Interneuron-specific therapeutics for normalizing neuronal cell excitability and treating dravet syndrome

Abstract

To provide therapeutic compositions and methods capable of modulating the activity of GABAergic interneurons or other cortical neurons.SOLUTION: Therapeutic virus vectors are provided, particularly recombinant adeno-associated virus (rAAV) vectors designed to contain an enhancer sequence that specifically restricts expression of an effector gene (for example, an SCN1A-encoding polynucleotide, a Gq-DREADD-encoding polynucleotide, or a PSAM-encoding polynucleotide) contained in the vector to PV-expressing GABAergic interneurons or neuron cell populations in the brain.SELECTED DRAWING: None

Description

[Technical Field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This is an international PCT application claiming priority to and the benefit of U.S. Provisional Application No. 62 / 801,483, filed February 5, 2019, U.S. Provisional Application No. 62 / 823,281, filed May 25, 2019, and U.S. Provisional Application No. 62 / 916,477, filed October 17, 2019. The contents of each of these provisional applications are incorporated herein by reference in their entirety.

[0002] STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH This invention was made with United States government support under Grant No. MH111529 awarded by the National Institutes of Health. The United States government has certain rights in this invention. [Background technology]

[0003] background There is a delicate balance between excitation and inhibition that must be carefully maintained for brain circuits to function properly and for the neuronal cells functioning within these circuits to be active. Alterations, defects, or disruptions in the balance of excitation and inhibition in brain circuits have been shown to result in numerous neurological, neurodevelopmental, or neurodegenerative diseases and disorders. Furthermore, lack of proper cortical interneuron function has been linked to neurodevelopmental and neurological diseases and disorders.

[0004] Abnormal or unusual function and activity of interneurons can arise as a result of deviations from the interneuron developmental pathway (e.g., aberrant fate specification during embryonic development due to genetic mutations) or acute insults (e.g., stroke, concussion). Alterations in unusual GABAergic neurotransmission and inhibitory cortical circuits can cause or induce clinical features and symptoms, e.g., seizures and epilepsy, that afflict patients with serious neurological diseases and disabilities, such as Dravet syndrome (DS), a pharmaco-resistant form of infantile epilepsy associated with cognitive impairment and premature death.

[0005] The lack of therapeutic compositions and methods that can regulate the activity of GABAergic interneurons or other cortical neurons with specificity and sensitivity has seriously hindered the medical community's ability to alleviate seizures in a wide variety of epilepsy cases, particularly in patients with focal seizures and DS.Such compositions and methods are urgently needed to combat and treat these devastating conditions as well as the severe symptoms of other neuropsychiatric disorders.The products, compositions, and methods described herein are provided to address and meet these needs. Summary of the Invention

[0006] Summary of the Disclosure and Aspects The present specification focuses on viral vectors, particularly recombinant adeno-associated viral (rAAV) vectors, their viral particles, and compositions and methods. The rAAV vectors contain (or are molecularly engineered to contain) at least one transgene (e.g., an effector gene, such as hM3Dq-modified muscarinic receptor (Gq-DREADD), a pharmacologically selective actuator molecule (PSAM), or a therapeutic gene, such as SCN1A) and a specific regulatory polynucleotide sequence that restricts transgene expression to interneuron (IN) cells, particularly fast-spiking parvalbumin-expressing GABAergic interneurons (referred to herein as PV interneurons (PV IN)) or neuronal cells of the cerebral cortex. In one embodiment, the specific regulatory polynucleotide sequence is derived from an enhancer sequence near the gene SCN1A, and restricts the expression of the transgene carried by the rAAV to a population of fast-spiking parvalbumin-expressing GABAergic interneurons in the brain. In one embodiment, the therapeutic gene is SCN1A. In a specific embodiment, the vector specifically transduces interneuron cells, particularly cortical interneuron cells, that are deficient or defective in the expression of the SCN1A gene encoding the sodium chloride channel Nav1.1, thereby normalizing the excitability of interneurons that are deficient or defective in SCN1A, thereby alleviating seizures and seizure symptoms in subjects with Dravet syndrome (DS).

[0007] In one aspect, to restrict transgene expression to GABAergic PV-expressing interneurons, or pyramidal (PYR) neurons, or vasoactive intestinal peptide (VIP)-expressing cortical interneurons in a mammal, a suitable viral vector, e.g., a lentiviral vector, or, in particular, a recombinant adeno-associated viral (rAAV) vector, is used and includes an enhancer element polynucleotide (also referred to herein as a regulatory element) described herein. In one embodiment, the enhancer element is provided in cis. In one embodiment, the regulatory element is S5E1, S5E2, S5E3, S5E4, S5E5, S5E6, S5E7, S5E8, S5E9, or S5E10 described herein, in particular human E1-E10. In one embodiment, the enhancer element is human E11-E35 described herein. In one embodiment, the enhancer element is S5E1 (E1). In one embodiment, the enhancer element is S5E2 (E2). In one embodiment, the enhancer element is S5E3 (E3). In one embodiment, the enhancer element is S5E4 (E4). In one embodiment, the enhancer element is E5. In one embodiment, the enhancer element is E6. In one embodiment, the enhancer element is E11. In one embodiment, the enhancer element is E14. In one embodiment, the enhancer element is E22. In one embodiment, the enhancer element is E29.

[0008] In one aspect, the enhancer-containing viral or rAAV vector expresses one copy of SCN1A in transduced PV-expressing interneuron cells for the treatment and therapy of DS. In other embodiments, the enhancer-containing viral or rAAV vector expresses an effector gene, e.g., a Gq-DREADD receptor, or, e.g., a pharmacologically selective actuator molecule (PSAM), an orthogonal ligand-gated ion channel (and its pharmacologically selective effector molecule (PSEM)), for chemogenetic modulation of PV interneuron activity for the treatment of all types of epilepsy, including focal epilepsy and pharmacologically refractory epilepsy, and for the treatment of DS.

[0009] In one aspect, a viral vector is provided that comprises a transgene polynucleotide sequence and an enhancer polynucleotide sequence that specifically restricts expression of the transgene to parvalbumin (PV)-expressing interneuron cells in the brain.

[0010] In one aspect, a viral vector is provided that comprises an enhancer polynucleotide sequence specifically associated with SCN1A gene expression and a transgene polynucleotide sequence, wherein the enhancer sequence restricts expression of the transgene to PV-expressing interneuron cells in the brain.

[0011] In one aspect, a suitable viral vector, e.g., a lentiviral vector, or, in particular, a recombinant adeno-associated viral (rAAV) vector, is used to restrict transgene expression to GABAergic vasoactive intestinal peptide-expressing cortical interneuron cells (VIP cINs) in the mammalian brain, where an enhancer element described herein is provided in cis. In one embodiment, the enhancer element is S5E6, as described herein.

[0012] In one aspect, a suitable viral vector, e.g., a lentiviral vector, or, in particular, a recombinant adeno-associated viral (rAAV) vector, is used to restrict transgene expression to both GABAergic interneurons and glutamatergic pyramidal neurons of the mammalian brain, in which an enhancer element described herein is provided in cis. In one embodiment, the pyramidal neurons are in cortical layer 5 of the mammalian brain. In one embodiment, the enhancer element that restricts expression to pyramidal neurons is S5E5, as described herein.

[0013] In an embodiment of the viral vector of the above aspect, the transgene is a reporter gene, a Designer receptor exclusively activated by designer drug (DREADD)-encoding gene, a pharmacologically selective actuator molecule (PSAM)-encoding gene, or a therapeutic gene, e.g., SCN1A. In one embodiment, the transgene is an SCN1A gene. In one embodiment, the transgene is a DREADD-encoding polynucleotide. In one embodiment, the DREADD-encoding polynucleotide is a Gq-DREADD-encoding gene that is activated by the chemogen clozapine-N4-oxide (CNO). In one embodiment, the transgene is a pharmacologically selective actuator molecule (PSAM)-encoding gene. In one embodiment, the expressed PSAM specifically interacts with a PSEM ligand. In one embodiment, the viral vector is a recombinant adeno-associated virus (rAAV) vector.

[0014] In another aspect, a recombinant adeno-associated virus (rAAV) vector is provided comprising an SCN1A transgene polynucleotide sequence or a functional portion thereof and an enhancer polynucleotide sequence that specifically restricts expression of the SCN1A transgene to interneuron cells of the brain.

[0015] In an embodiment of the viral vector or rAAV vector of the above aspect, after transduction of an interneuron or neuronal cell with the viral vector or rAAV vector, the Nav1.1 sodium channel encoded by the SCN1A transgene is functionally expressed in the interneuron or neuronal cell. In an embodiment of the viral vector or rAAV vector of the above aspect, after transduction of an interneuron or neuronal cell with the viral vector or rAAV vector, the Nav1.1 sodium channel encoded by the SCN1A transgene is functionally expressed in both a GABAergic interneuron and a glutamatergic pyramidal neuron. In one embodiment, the interneuron cell is a GABAergic interneuron cell. In one embodiment, the interneuron cell is a GABAergic interneuron cell in the telencephalon of the brain. In one embodiment, the GABAergic interneuron cell expresses parvalbumin (PV). In one embodiment, the neuronal cell is a pyramidal neuron cell, for example, a glutamatergic pyramidal neuron in the brain cortex. In one embodiment of any of the above aspects, the enhancer polynucleotide sequence comprises the polynucleotide sequence of mouse enhancer element E1, E2, E3, E4, E5, E6, E7, E8, E9, or E10 (SEQ ID NOs:5-14, respectively), or an ortholog thereof, e.g., a human ortholog. In one embodiment, the enhancer polynucleotide sequence comprises the polynucleotide sequence of human enhancer element E1, E2, E3, E4, E5, E6, E7, E8, E9, or E10 (SEQ ID NOs:15-24, respectively). In one embodiment, the viral vector or rAAV vector comprises an enhancer polynucleotide sequence comprising a nucleotide sequence containing one or more regions of about 100 bp or more that have at least 75% or more sequence identity to the polynucleotide sequence of human enhancer element E1, E2, E3, E4, E5, E6, E7, E8, E9, or E10 (SEQ ID NOs:15-24, respectively).In another embodiment, the viral or rAAV vector comprises an enhancer polynucleotide sequence comprising a nucleotide sequence containing one or more regions of about 100 bp or more having at least 75% or more sequence identity to the polynucleotide sequence of human enhancer element E2 (SEQ ID NO:16). In another embodiment, the viral or rAAV vector comprises an enhancer polynucleotide sequence comprising a nucleotide sequence containing one or more regions of about 100 bp or more having at least 75% or more sequence identity to the polynucleotide sequence of human enhancer element E5 (SEQ ID NO:19). In another embodiment, the viral or rAAV vector comprises an enhancer polynucleotide sequence comprising a nucleotide sequence containing one or more regions of about 100 bp or more having at least 75% or more sequence identity to the polynucleotide sequence of human enhancer element E6 (SEQ ID NO:20). In an embodiment of the above aspect, the viral or rAAV vector comprises an enhancer polynucleotide sequence comprising the polynucleotide sequence of human enhancer element E2 (SEQ ID NO:16). In other embodiments of the above aspects, the viral or rAAV vector comprises an enhancer polynucleotide sequence comprising the polynucleotide sequence of human enhancer element E5 (SEQ ID NO:19) or the polynucleotide sequence of human enhancer element E6 (SEQ ID NO:20). In other embodiments of the above aspects, the viral or rAAV vector comprises any one (or more) of the enhancer polynucleotide sequences comprising the polynucleotide sequence of human enhancer elements E11 (SEQ ID NO:25) through E35 (SEQ ID NO:49). In one embodiment, the capacity of the vector to package polynucleotide sequences greater than about 4.7 kb includes reassortment of multiple rAAV vectors by homologous recombination or reassortment of multiple rAAV vectors by acceptor site-mediated splicing.In one embodiment, the vector delivers the SCN1A gene to SCN1A-expressing GABAergic interneurons or glutamatergic pyramidal neuron cells in the brain, where the SCN1A gene is functionally expressed, thereby restoring normal levels of SCN1A in interneurons and neuron cells after administering the vector to the subject.In one embodiment, the subject is a human patient.In one embodiment, the human patient is an infant suffering from Dravet syndrome (DS).

[0016] In another aspect, a viral or virus-like particle is provided that includes the viral vector or rAAV vector of any of the above aspects.

[0017] In another aspect, a cell is provided that comprises the viral vector or rAAV vector of any of the above aspects. In one embodiment, the cell comprises a viral particle as set forth above.

[0018] In another aspect, a pharmaceutical composition is provided that includes a viral vector or rAAV vector of any of the above aspects and a pharmaceutically acceptable vehicle, carrier, or diluent.

[0019] In another aspect, there is provided a pharmaceutical composition comprising the viral particles of any of the above aspects and a pharmaceutically acceptable vehicle, carrier, or diluent. In embodiments of the above aspects, the pharmaceutical composition is in liquid dosage form.

[0020] In one aspect, provided is a method for restoring normal levels of SCN1A expression in a GABAergic interneuron cell that has a deficient or defective level of SCN1A expression, the method comprising contacting the cell with an effective amount of any of the viral vectors or rAAV vectors or viral particles or pharmaceutical compositions thereof of the above aspects to restore normal levels of SCN1A expression in the GABAergic interneuron cell.

[0021] In one aspect, provided is a method of treating infantile epilepsy and / or seizures in an infant having or at risk of having epilepsy, seizures, or Dravet Syndrome (DS), comprising administering to the infant a therapeutically effective amount of a viral vector or rAAV vector of any of the above aspects, a viral particle of any of the above aspects, or a pharmaceutical composition of any of the above aspects to treat the seizures, epilepsy, or DS in the subject.

[0022] In one aspect, provided is a method of treating Dravet syndrome (DS) in a subject having or at risk of having DS, comprising administering to the subject a therapeutically effective amount of a viral vector or rAAV vector, or viral particle or pharmaceutical composition thereof, of any of the above aspects to treat DS in the subject.

[0023] In one aspect, provided is a method for inhibiting or preventing seizures and / or epilepsy in a subject having or at risk of having seizures and / or epilepsy, the method comprising systemically administering to the subject a recombinant adeno-associated virus (rAAV) vector comprising an SCN1A transgene polynucleotide sequence or a functional portion thereof, an enhancer polynucleotide sequence that specifically restricts expression of the SCN1A transgene to interneuronal cells of the cerebral cortex of the subject, and a capsid that enhances transduction of the vector into interneuronal cells.

[0024] In one embodiment of the methods of any of the above aspects, the infant or subject is a human patient. In one embodiment of the methods of any of the above aspects, the enhancer polynucleotide sequence present in the viral vector or rAAV vector is selected from human enhancer elements E1, E2, E3, E4, E5, E6, E7, E8, E9, or E10, or E11-E35 (SEQ ID NOs:25-49, respectively). In one embodiment, the viral vector or rAAV vector comprises an enhancer polynucleotide sequence comprising a nucleotide sequence containing one or more regions of about 100 bp or more having at least 75% or more sequence identity to the polynucleotide sequence of human enhancer elements E1, E2, E3, E4, E5, E6, E7, E8, E9, or E10 (SEQ ID NOs:15-24, respectively) or E11-E35 (SEQ ID NOs:25-49, respectively). In one embodiment, the enhancer polynucleotide sequence is a human E2 enhancer polynucleotide sequence, or the enhancer polynucleotide sequence contains one or more regions of about 100 bp or more having at least 75% or more sequence identity to the polynucleotide sequence of human enhancer elements E1, E2, E3, E4, E5, E6, E7, E8, E9, or E10 (SEQ ID NOs:15-24, respectively) or E11-E35 (SEQ ID NOs:25-49, respectively). In one embodiment, the enhancer polynucleotide sequence is a human E5 enhancer polynucleotide sequence. In one embodiment, the enhancer polynucleotide sequence is a human E6 enhancer polynucleotide sequence. In certain embodiments, the enhancer polynucleotide sequence contains one or more regions of about 100 bp or more having at least 75% or more sequence identity to the polynucleotide sequence of human enhancer element E2 (SEQ ID NO:16).In other embodiments, the enhancer polynucleotide sequence contains one or more regions of about 100 bp or more that have at least 75% or more sequence identity to the polynucleotide sequence of human enhancer element E5 (SEQ ID NO:19) or the polynucleotide sequence of human enhancer element E6 (SEQ ID NO:20).

[0025] In one aspect, there is provided a method for delivering a transgene for restricted expression in interneuronal or neuronal cells expressing the SCN1A gene to inhibit or prevent seizures and / or epilepsy in a subject in need thereof, the method comprising contacting cells with a recombinant adeno-associated virus (rAAV) vector comprising an SCN1A transgene polynucleotide sequence or a functional portion thereof and an enhancer polynucleotide sequence that specifically restricts expression of the SCN1A transgene to interneuronal or neuronal cells of the cerebral cortex of the subject, thereby inhibiting or preventing seizures and / or epilepsy in the subject.

[0026] In one embodiment of the method of any of the above aspects, the rAAV vector, viral particle, virus-like particle, or pharmaceutical composition is administered systemically. In one embodiment of the method of any of the above aspects, the rAAV vector, viral particle, virus-like particle, or pharmaceutical composition is administered parenterally or intravenously. In one embodiment of the method of any of the above aspects, the rAAV vector, viral particle, or pharmaceutical composition is administered intracerebrally. In one embodiment of the method of any of the above aspects, the rAAV vector, viral particle, or pharmaceutical composition is administered as a prophylactic. In one embodiment of the method of any of the above aspects, the method further comprises administering adjunctive antiepileptic treatment to the infant or subject.

[0027] In another aspect, a viral vector is provided comprising a transgene polynucleotide sequence and an enhancer polynucleotide sequence that specifically restricts transgene expression to vasoactive intestinal peptide-expressing cortical interneuron cells (VIP cINs) in the brain. In another aspect, a viral vector is provided comprising an enhancer polynucleotide sequence specifically associated with SCN1A gene expression and a transgene polynucleotide sequence, wherein the enhancer sequence restricts transgene expression to vasoactive intestinal peptide-expressing cortical interneuron cells (VIP cINs) in the brain. In one embodiment, the enhancer polynucleotide sequence comprises a nucleotide sequence containing one or more regions of about 100 bp or more that have at least 75% or more sequence identity to the polynucleotide sequence of human enhancer element E6 (SEQ ID NO:20). In a specific embodiment, the enhancer polynucleotide sequence is human enhancer element E6 (SEQ ID NO:20). In one embodiment, the viral vector is a recombinant adeno-associated virus (rAAV) vector. In one embodiment, the transgene is the SCN1A gene.

[0028] In another aspect, a viral vector is provided comprising a transgene polynucleotide sequence and an enhancer polynucleotide sequence that specifically restricts transgene expression to pyramidal neurons of the brain. In another aspect, a viral vector is provided comprising an enhancer polynucleotide sequence specifically associated with SCN1A gene expression and a transgene polynucleotide sequence, wherein the enhancer sequence restricts transgene expression to pyramidal neurons of the brain. In one embodiment, the enhancer polynucleotide sequence comprises a nucleotide sequence containing one or more regions of about 100 bp or more that have at least 75% or more sequence identity to the polynucleotide sequence of human enhancer element E5 (SEQ ID NO: 19). In a specific embodiment, the enhancer polynucleotide sequence is human enhancer element E5 (SEQ ID NO: 19). In another specific embodiment, the enhancer sequence restricts transgene expression to pyramidal neurons in cortical layer 5 of the brain. In one embodiment, the viral vector is a recombinant adeno-associated virus (rAAV) vector. In one embodiment, the transgene is the SCN1A gene.

[0029] In one aspect, a viral vector is provided that specifically targets SCN1A-expressing neuronal cells, the viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NOs: 15 to 24, or a functional portion thereof. In one embodiment, the neuronal cells are parvalbumin cortical interneurons (PV cINs), pyramidal (PYR) neurons, or vasoactive intestinal peptide cortical interneurons (VIP cINs).

[0030] In one aspect, there is provided a viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NOs: 25 to 27 or a functional portion thereof, which specifically targets Pvalb-expressing cells.

[0031] In one aspect, there is provided a viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NOs: 28-31 or a functional portion thereof, which specifically targets Acan-expressing cells.

[0032] In one aspect, there is provided a viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NOs: 32 to 39 or a functional portion thereof, which specifically targets Tmem132c-expressing cells.

[0033] In one aspect, a viral vector is provided that comprises an enhancer polynucleotide sequence selected from SEQ ID NO:40 or SEQ ID NO:41, or a functional portion thereof, and that specifically targets Lrrc38-expressing cells.

[0034] In one aspect, a viral vector is provided that comprises an enhancer polynucleotide sequence selected from SEQ ID NO:42 or SEQ ID NO:43, or a functional portion thereof, and that specifically targets Inpp5j-expressing cells.

[0035] In one aspect, there is provided a viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NOs: 44 to 47 or a functional portion thereof, which specifically targets Mef2c-expressing cells.

[0036] In one aspect, there is provided a viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NO:48 or SEQ ID NO:49, or a functional portion thereof, which specifically targets Pthlh-expressing cells.

[0037] In one aspect, there is provided a viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NOs: 15 to 49, or a functional portion thereof, which specifically targets PV-expressing cells.

[0038] In any embodiment of the viral vector of any of the above aspects, the target cell is a PV-expressing neuronal cell. In embodiments of the viral vector of any of the above aspects, the viral vector is a lentiviral vector or a recombinant adeno-associated viral (rAAV) vector.

[0039] In one aspect, a cell is provided that comprises the viral vector of any of the above aspects and embodiments.

[0040] In one aspect, there is provided a virus or virus-like particle comprising the viral vector of any of the above aspects and embodiments. In one aspect, there is provided a cell comprising a virus or virus-like particle comprising the viral vector of any of the above aspects and embodiments.

[0041] In one aspect, there is provided a pharmaceutical composition comprising the viral vector or virus or virus-like particle of any of the above aspects and embodiments and a pharmaceutically acceptable vehicle, carrier, or diluent.

[0042] In another aspect, a method for restricting expression of a transgene to neuronal cells of a subject is provided, comprising administering to the subject a delivery vector comprising at least one enhancer element polynucleotide comprising the sequence of SEQ ID NOs: 15-49 and a transgene polynucleotide, wherein the transgene is specifically expressed in neuronal cells. In one embodiment of the method, the transgene is SCN1A. In one embodiment, the neuronal cells are parvalbumin-expressing cortical interneurons (PV cINs). In one embodiment, the enhancer element polynucleotide comprises the sequence set forth in SEQ ID NOs: 15-18 or SEQ ID NOs: 21-24.

[0043] In another embodiment of the above method, the neuronal cell is a pyramidal (PYR) cell. In one embodiment, the enhancer element polynucleotide comprises the sequence shown in SEQ ID NO:19.

[0044] In another embodiment of the above method, the neuronal cell is a vasoactive intestinal peptide-expressing cortical interneuron (VIP cIN). In one embodiment, the enhancer element polynucleotide comprises the sequence shown in SEQ ID NO:20.

[0045] In one embodiment of the above method and its embodiments, the delivery vector is a lentiviral vector or rAAV.In one embodiment of the method, the delivery vector is administered to the brain.In one embodiment of the method, the delivery vector is administered locally or systemically.In one embodiment, the subject is a mammal.In one embodiment, the subject is a human.

[0046] In another aspect, a viral vector is provided comprising a human enhancer polynucleotide sequence selected from SEQ ID NOs: 15-49. In one embodiment, the viral vector is a recombinant adeno-associated viral (rAAV) vector. In an embodiment, a viral particle or virus-like particle comprises the viral vector described above. In another embodiment, a cell comprises the viral vector described above. In one embodiment, a cell comprises the viral particle or virus-like particle described above. In one embodiment, a pharmaceutical composition comprises the viral vector described above or the viral particle or virus-like particle described above and a pharmaceutically acceptable vehicle, carrier, or diluent.

[0047] definition Unless otherwise defined, all technical and scientific terms used herein have the meanings commonly understood by those skilled in the art to which the described aspects and embodiments belong.The following references provide those skilled in the art with the general definitions of many of the terms used in the described embodiments: Singleton et al., Dictionary of Microbiology and Molecular Biology (2nd ed. 1994); The Cambridge Dictionary of Science and Technology (Walker ed., 1988); The Glossary of Genetics, 5th Ed., R. Rieger et al. (eds.), Springer Verlag (1991); and Hale & Marham, The HarperCollins Dictionary of Biology (1991).As used herein, the following terms have the meanings ascribed to them below, unless otherwise specified.

[0048] "Administering" means giving, providing, dispensing, or applying or contacting a composition, agent, therapeutic product, such as a viral vector (rAAV) carrying a transgene (e.g., an effector or therapeutic gene), to a subject. Administering or administration can be accomplished by any of a number of routes, including, but not limited to, parenteral or systemic, intravenous (IV), (injection), subcutaneous, intrathecal, intracranial, intramuscular, cutaneous, intradermal, inhalation, rectal, intravaginal, topical, oral, subcutaneous, intramuscular, or intraocular. In embodiments, administration is systemic, e.g., by inoculation, injection, or intravenous injection.

[0049] By "agent" is meant a peptide, polypeptide, nucleic acid molecule, or small molecule compound, antibody, or fragment thereof.

[0050] By "alteration" is meant a change (increase or decrease) in the expression level or activity of a gene or polypeptide as detected by standard, art-known methods, such as those described herein. As used herein, alteration includes a 10% change in expression level, a 25% change in expression level, a 40% change, or a 50% or greater change in expression level.

[0051] "Ameliorate" and "amelioration" mean to lessen, inhibit, attenuate, reduce, arrest, or stabilize the onset or progression of a disease.

[0052] "Analog" or "derivative" refers to a molecule that is not identical but has similar functional or structural characteristics. For example, a polypeptide analog retains the biological activity of the corresponding native polypeptide but has certain biochemical modifications that enhance the analog's function compared to the native polypeptide. Such biochemical modifications can, for example, increase the analog's protease resistance, membrane permeability, or half-life without altering its polynucleotide binding activity. In another example, a polynucleotide analog retains the biological activity of the corresponding native polynucleotide but has certain modifications that enhance the analog's function compared to the native polynucleotide. Such modifications can increase the polynucleotide's affinity for DNA, half-life, and / or nuclease resistance, and the analog may contain unnatural nucleotides or amino acids.

[0053] As used herein, the term "at risk," when applied to a neurological or neurodevelopmental disease, disorder, or condition, such as seizures or epilepsy, refers to a patient or individual who has a family history of or genetic risk factor genes for a neurological or neurodevelopmental disease, disorder, or condition.

[0054] The term "carrier" as used herein refers to a diluent, adjuvant, excipient, or vehicle that can be administered with a composition or pharmaceutical composition, such as a composition or pharmaceutical composition containing a polynucleotide, a viral vector, or a viral particle. Pharmaceutical carriers and pharmaceutically acceptable carriers include sterile liquids, such as water and oils, including those of petroleum, animal, vegetable, or synthetic origin, such as peanut oil, soybean oil, mineral oil, sesame oil, and the like. For injectable solutions, water or saline and aqueous dextrose and glycerol solutions may be used as carriers, particularly for injectable solutions. Carriers may also include solid dosage forms, including, but not limited to, one or more of a binder (for compressed pills), a glidant, an encapsulating agent, a flavorant, and a colorant. Suitable pharmaceutical carriers are described in "Remington's Pharmaceutical Sciences" by E.W. Martin.

[0055] As used herein, "comprises," "comprising," "containing," "having," and the like may have the meaning ascribed to those terms in U.S. patent law and may mean "includes," "including," and the like. Similarly, "consisting essentially of" or "consists essentially" have the meaning ascribed to those terms in U.S. patent law. This term is open-ended, allowing for more than what is recited to be present so long as the basic or novel characteristics of the recited items are not altered by the presence of more than what is recited but excluding aspects of the prior art.

[0056] "DREADD" is an acronym for "designer receptor exclusively activated by a designer drug" and refers to a modified G protein-coupled receptor (GPCR) that can be administered or specifically introduced into a subject or its cells, such as PV-expressing interneurons, using a viral vector (containing a polynucleotide sequence encoding the DREADD) or by genetic breeding. DREADDs are known as chemical genetic, or "chemogenetic," molecules that allow for precise temporal control of neuronal excitation and inhibition. After DREADD expression, the DREADD can be activated by a specific ligand (or agonist), which can be administered intravenously or orally. DREADDs and their ligands are designed to be orthogonal, i.e., they bind specifically to each other and do not cross-react. As a non-limiting example, five different classes of DREADDs can be used: hM3Dq increases intracellular calcium levels and induces burst firing; hM4Di reduces cAMP and the activation of certain potassium channels, causing neuronal silencing and inhibiting presynaptic neurotransmitter release. GsD elevates cAMP, resulting in modulation signaling. Rq(R165L) elevates arrestin signaling, a specific pathway implicated in psychotropic mechanisms. κ-opioid receptor DREADDs or KORDs reduce or inhibit neuronal excitation and also inhibit presynaptic neurotransmitter release (see, e.g., Kelly Rae Chi, 2015, The Scientist; and SM Sternson and BL Roth, 2014, Ann Rev Neuroscience, 37:387-407).

[0057] Orthogonal ligand-gated ion channels are termed pharmacologically selective actuator molecules (PSAMs) and pharmacologically selective effector molecules (PSEMs), and similar to the use of DREADDs, are other types of chemogenetic molecules used as optogenetic agents and in optogenetic methods. Each PSAM is activated exclusively by a PSEM-cognate synthetic agonist. As an example, three specific PSAM / PSEM tools have been designed, each with distinct ion conductance properties for controlling neuronal excitability (see, e.g., Shapiro, MG et al., 2012, ACS Chem. Neurosci., 3(8):619-629). These include cation-selective activators, PSAMs, and cation-selective effector molecules. Q79G,Q139G -5HT3HC / PSEM 22S , anion-selective silencer, PSAM L141F,Y115F -GlyR / PSEM 89S , and the third Ca 2+ PSAM is a selective channel Q79G,L141S -nAChR V13'T / PSEM 9S (See ibid. and Magnus, CJ et al., 2011, Science, 333(6047):1292-1296). Both DREADDs and PSAM-PSEMs allow for temporal control of neuronal activity from minutes to hours (see, e.g., Kelly Rae Chi, 2015, The Scientist; and SM Sternson and BL Roth, 2014, Ann Rev Neuroscience, 37:387-407). For example, various PSAMs have been used with various ion channels and PSEMs to control E / I balance in neurons, e.g., neurons. Such PSAM-PSEM pairs include ligand-PSEMs. 89S PSAMs are activated by , allowing cations to enter the cell and enhance excitability. L141F,Y115F -5HT3 HC; Ligand PSEM 89S PSAMs are activated by β-glucan and silence neuronsL141F,Y115F -GlyR; and PSAM, which is activated by the ligand PSEM9S and enhances calcium signaling Q79G,L141S -nAChR V13. Since there are two different PSEM ligands, PSAM-PSEM can also be combined in the same animal (subject).

[0058] "Detecting" refers to determining the presence, absence, or amount of the molecule, compound, or agent being detected.

[0059] "Disease" refers to any condition or disorder that adversely affects, damages, or interferes with the normal function of a cell, tissue, organ, or part of the body, such as the brain, including the cerebral cortex and brain tissue of the brain. In one embodiment, the disease is seizures or epilepsy. In another embodiment, the disease is Dravet syndrome.

[0060] By "effective amount" is meant the amount required to ameliorate disease symptoms compared to untreated patients. For therapeutic treatment of disease, the effective amount of an active compound used in practicing the described methods will vary depending on the method of administration, the age, weight, and general health of the subject. Ultimately, the attending physician, clinician, or veterinarian will determine the appropriate amount and administration regimen. Such an amount is referred to as an "effective" amount. In one embodiment, an effective amount is the amount of an rAAV vector containing a specific enhancer sequence (e.g., an SCN1A-specific enhancer, e.g., E1-E10 described herein) and one or more transgene sequences (e.g., SCN1A) inserted therein that is necessary to reduce, ameliorate, alleviate, inhibit, or stabilize the symptoms or severity of a neurological disease or disorder, e.g., seizures, epilepsy, or Dravet syndrome (DS). In another embodiment, an effective amount is the amount of an rAAV vector comprising a specific enhancer sequence (e.g., an SCN1A-specific enhancer, e.g., E1-E10 described herein) and one or more transgene sequences (e.g., SCN1A) inserted therein necessary to cause specific inhibitory activity in interneuron cells, e.g., GABAergic interneuron cells or PV-expressing GABAergic interneuron cells. In one embodiment, the enhancer is E2 described herein, which restricts expression of a transgene, e.g., SCN1A, or, in the case of chemogenetic modulation of PV interneuron activity, an effector such as Gq-DREADD or PSAM, to PV interneuron cells.

[0061] As used herein, the term "endogenous" refers to a molecule (e.g., a polypeptide, peptide, nucleic acid, or cofactor) that is found in nature in a particular organism (e.g., a human) or in a particular location within an organism (e.g., an organ, tissue, or cell, e.g., a human cell).

[0062] As used herein, the term "exogenous" refers to a molecule (e.g., a polypeptide, peptide nucleic acid, or cofactor) that is not found naturally, or endogenously, in a particular organism (e.g., a human) or in a particular location within an organism (e.g., an organ, tissue, or cell, e.g., a human cell). Exogenous materials include those provided to an organism from an external source or to a culture extracted therefrom.

[0063] A "regulatory element," "regulatory sequence," "enhancer," "enhancer element," or "enhancer sequence" refers to a nucleic acid or polynucleotide sequence of approximately 50 to 2500 nucleotides, or a region of a nucleic acid or polynucleotide sequence, e.g., DNA or RNA, containing one or more binding sites recognized and bound by one or more binding proteins, e.g., transcription factors. Generally, binding proteins function as activators, increasing the likelihood that transcription of a specific target gene will occur. Enhancers can activate transcription regardless of the enhancer's location, distance, or orientation relative to the gene's promoter. For example, enhancer sequences can be located upstream of a gene, downstream of a gene, within the gene's coding region, or up to one million base pairs away from the gene. Typically, binding of a DNA-binding protein or transcription factor to an enhancer alters or modifies DNA conformation, thereby allowing interactions between or among the DNA-bound transcription factors.

[0064] Enhancers have been described as clusters of DNA sequences that can bind combinations of transcription factors, which then interact with components of the Mediator complex or TFIID to help recruit RNA polymerase II (RNAPII). To accomplish this, enhancer-bound transcription factors circularize the intervening sequences and contact the gene's promoter region, thus enabling enhancers to function in a distance-independent manner. Furthermore, eukaryotic gene activation requires decompaction of the chromatin fiber, which is carried out by enhancer-bound transcription factors, recruiting histone-modifying enzymes or ATP-dependent chromatin remodeling complexes to alter chromatin structure and increase DNA accessibility to other proteins. (For a review of enhancer function, see, e.g., Ong, C.-T. and Corces, VG, 2011, Nat. Rev. Genetics, 12(4):283-293.)

[0065] As described herein, ten enhancers near the SCN1A gene were screened for their ability to restrict expression of a transgene, i.e., SCN1A, to PV-expressing interneuron cells (PV cells), most of which express the SCN1A gene. The isolated enhancer sequences, designated herein as S5E1 (E1) through S5E10 (E10), were found to be capable of restricting SCN1A expression to GABAergic interneurons. As an example, the E2 enhancer (S5E2) was demonstrated to target and restrict transgene expression to PV-expressing interneurons that express SCN1A. It is understood that a significant fraction of cells expressing SCN1A are not PV-expressing interneurons. In one aspect, the enhancers described herein enable the restriction of expression of a transgene, e.g., SCN1A, or another effector gene, e.g., Gq-DREADD or PSAM, to PV interneurons rather than to all SCN1A-expressing neurons. As another example, isolated E5 enhancer (S5E5) has been shown to target and restrict transgene expression to glutamatergic pyramidal neurons in the brain.In an embodiment, such enhancer is E1, E2, E3, E4, E5, E6, E7, E8, E9, or E10 as described herein.In one embodiment, enhancer element is isolated from its natural environment.Such enhancer element is used in vectors, for example, viral vectors, to deliver to cells, tissues, or body regions, for example, the brain.

[0066] By "fragment" is meant a portion of a polypeptide or nucleic acid molecule, which portion contains at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or 90% of the entire length of the reference nucleic acid molecule or polypeptide. A fragment may contain 10, 20, 30, 40, 50, 60, 70, 80, 90, or 100, 200, 300, 400, 500, 600, 700, 800, 900, or 1000 nucleotides or amino acids.

[0067] "Functionally expressed" means that a gene or transgene contained within or inserted into a polynucleotide of an rAAV or rAAV vector described herein is expressed in an infected or transduced cell to produce its encoded product, which product is functional and / or active in the cell. In one embodiment, the cell is an interneuron cell. In one embodiment, the cell is a GABAergic interneuron cell. In one embodiment, the cell is a GABAergic interneuron cell that expresses parvalbumin (PV). In one embodiment, the cell is a neuron, particularly a glutamatergic pyramidal interneuron cell. In one embodiment, the transgene is a detectable reporter gene, such as d-Tomato, ChR2, GFP, RFP, etc. In one embodiment, the transgene is a designer receptor exclusively activated by designer drugs (DREADD) or Gq-DREADD. In one embodiment, the transgene is a PSAM. In one embodiment, the transgene is SCN1A, which encodes the sodium channel Nav1.1.

[0068] "Hybridization" refers to hydrogen bonding between complementary nucleobases, which may be Watson-Crick, Hoogsteen, or reversed Hoogsteen hydrogen bonds. For example, adenine and thymine are complementary nucleobases that pair by forming hydrogen bonds.

[0069] The term "interneuron" refers to a neuron (nerve cell) that relays impulses between sensory neurons and motor neurons, i.e., a local circuit neuron in the central nervous system (CNS). Generally, neurons are specialized cells that function primarily in transmitting nerve impulses. Neurons have cell processes, such as dendrites and axons. Dendrites are short processes at the neuron's cell body that receive input from other neurons and transmit signals to the cell body. The axon is the longer, single process at the cell body that relays signals toward the neuron's tip (called the synaptic terminal). Three main types of neurons include sensory neurons, interneurons (of the CNS), and motor neurons. The human brain contains approximately 100 billion interneurons, which receive impulses from sensory neurons. Interneurons interpret information received from other neurons and relay impulses to motor neurons for appropriate responses in a function called "integration."

[0070] The terms "isolated," "purified," or "biologically pure" refer to material that is free, to varying degrees, from components that normally accompany or are associated with it as found in the natural state. "Isolated" refers to some degree of separation from the original source or surroundings. "Purified" refers to a greater degree of separation than isolation. A "purified" or "biologically pure" protein or polynucleotide is sufficiently free from other materials so that any impurities do not materially affect the biological properties of the protein or polynucleotide or cause other adverse events. That is, a polynucleotide (nucleic acid), polypeptide, or peptide is purified if it is substantially free of cellular material, viral material, and culture medium when produced by recombinant DNA methods, or substantially free of chemical precursors and other chemicals when chemically synthesized. Purity and homogeneity are typically determined using analytical chemistry methods, such as polyacrylamide gel electrophoresis or high-performance liquid chromatography. The term "purified" can refer to the nucleic acid, protein, or peptide giving rise to essentially one band in an electrophoretic gel. In the case of proteins that can be subject to modifications, such as phosphorylation or glycosylation, different modifications may result in different isolated proteins, which can be purified separately.

[0071] An "isolated polynucleotide" refers to a nucleic acid (e.g., DNA) that is free of the genes that flank it in the naturally occurring genome of the organism from which the nucleic acid molecule, e.g., a nucleic acid molecule described herein, is derived. Thus, the term includes, for example, recombinant DNA integrated into a vector; a self-replicating plasmid or virus; or the genomic DNA of a prokaryote or eukaryote, or existing as a separate molecule independent of other sequences (e.g., cDNA or genomic or cDNA fragments generated by PCR or restriction endonuclease digestion). Furthermore, the term includes RNA molecules transcribed from DNA molecules, as well as recombinant DNA that is part of a hybrid gene encoding additional polypeptide sequences.

[0072] "Isolated polypeptide" refers to a polypeptide that has been separated from components that naturally accompany it. Typically, a polypeptide is isolated when it is at least 60%, by weight, free from the proteins and naturally-occurring organic molecules with which it is naturally associated. Preferably, the preparation is at least 75%, or at least 85%, or at least 90%, or at least 99%, by weight, the desired polypeptide. Isolated polypeptides may be obtained, for example, by extraction from a natural source, by expression of a recombinant nucleic acid encoding such a polypeptide, or by chemically synthesizing the protein. Purity can be measured by any appropriate method, for example, column chromatography, polyacrylamide gel electrophoresis, or HPLC analysis.

[0073] By "marker" is meant any protein or polynucleotide having an alteration in expression, level, or activity that is associated with a disease or disorder. In one embodiment, the marker is an SCN1A polynucleotide or SCN1A polypeptide.

[0074] The term "mutation" as used herein refers to the substitution of a nucleotide base in a sequence, e.g., a nucleotide base in a nucleic acid sequence or an amino acid residue in an amino acid sequence, for another residue, or the deletion or insertion of one or more residues in a sequence. Mutations are typically described herein by identifying the original residue followed by the position of the residue in the sequence and the identity of the newly substituted residue. Various methods for making the amino acid substitutions (mutations) provided herein are well known in the art and can be found, for example, in Green and Sambrook, Molecular Cloning: A Laboratory Manual (4 th ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY (2012)).

[0075] As used herein, "obtaining," as in "obtaining a drug," includes synthesizing, purchasing, or otherwise obtaining a drug.

[0076] "Polynucleotide" refers to a nucleic acid molecule, e.g., a double-stranded (ds) DNA polynucleotide, a single-stranded (ss) DNA polynucleotide, a dsRNA polynucleotide, or a ssRNA polynucleotide, that encodes one or more polypeptides. The term encompasses positive-sense (i.e., protein-encoding) DNA polynucleotides that can be transcribed to form RNA transcripts, which can then be translated to produce polypeptides after one or more optional RNA processing events (e.g., intron excision by RNA splicing, or ligation of a 5' cap or 3' polyadenylation tail). The term further encompasses positive-sense RNA polynucleotides that can be directly translated to produce polypeptides after one or more optional RNA processing events. As used herein, a polynucleotide may be contained within a viral vector, such as a recombinant adeno-associated viral vector (rAAV).

[0077] As used herein, the terms "nucleic acid" and "nucleic acid molecule" refer to a compound comprising a nucleobase and an acidic moiety, e.g., a nucleoside, a nucleotide, or a polymer of nucleotides. Typically, polymeric nucleic acids, e.g., nucleic acid molecules comprising three or more nucleotides, are linear molecules in which adjacent nucleotides are linked to each other by phosphodiester bonds. In some embodiments, "nucleic acid" refers to an individual nucleic acid residue (e.g., a nucleotide and / or a nucleoside). In some embodiments, "nucleic acid" refers to an oligonucleotide chain comprising three or more individual nucleotide residues. As used herein, the terms "oligonucleotide" and "polynucleotide" can be used interchangeably to refer to a polymer of nucleotides (e.g., a string of at least three nucleotides). In some embodiments, "nucleic acid" encompasses RNA and single-stranded and / or double-stranded DNA. Nucleic acids can be naturally occurring, e.g., in the context of a genome, transcript, mRNA, tRNA, rRNA, siRNA, snRNA, plasmid, cosmid, chromosome, chromatid, or other naturally occurring nucleic acid molecule. On the other hand, a nucleic acid molecule may be a non-natural molecule, e.g., recombinant DNA or RNA, an artificial chromosome, an engineered genome, or a fragment thereof, or a synthetic DNA, RNA, or DNA / RNA hybrid, and may contain non-natural nucleotides or nucleosides. Furthermore, the terms "nucleic acid," "DNA," "RNA," and / or similar terms include nucleic acid analogs, e.g., analogs having other than a phosphodiester backbone. Nucleic acids may be purified from natural sources, produced using recombinant expression systems, and optionally purified, chemically synthesized, etc. Where appropriate, e.g., in the case of chemically synthesized molecules, nucleic acids may contain nucleoside analogs, e.g., analogs having chemically modified bases or sugars and backbone modifications. Nucleic acid sequences are presented in the 5' to 3' direction unless otherwise specified.In some embodiments, nucleic acids include natural nucleosides (e.g., adenosine, thymidine, guanosine, cytidine, uridine, deoxyadenosine, deoxythymidine, deoxyguanosine, and deoxycytidine); nucleoside analogs (e.g., 2-aminoadenosine, 2-thiothymidine, inosine, pyrrolo-pyrimidine, 3-methyladenosine, 5-methylcytidine, 2-aminoadenosine, C5-bromouridine, C5-fluorouridine, C5-iodouridine, C5-propynyl-uridine, C5-propynyl-cytidine, C ...bromouridine, C5-bromouridine, C5-bromouridine, C5-bromouridine, C5-bromouridine, C5-bromouridine, C5-thiouridine, C5-thiouridine, C5-thiouridine, C5-thiouridine, C5-bromouridine, C5-bromouridine, C5-thiouridine, C5-bromour the bases are or contain: 7-deazaadenosine, 7-deazaguanosine, 8-oxoadenosine, 8-oxoguanosine, O(6)-methylguanine, and 2-thiocytidine; chemically modified bases; biologically modified bases (e.g., methylated bases); intercalated bases; modified sugars (2'-e.g., fluororibose, ribose, 2'-deoxyribose, arabinose, and hexose); and / or modified phosphate groups (e.g., phosphorothioate and 5'-N-phosphoramidite linkages).

[0078] As used herein, the term "pharmaceutically acceptable" refers to molecular entities, biological products, and compositions that are physiologically tolerable and that, when administered to a patient (e.g., a human patient), typically do not produce an allergic or other adverse reaction, e.g., stomach upset, dizziness, etc.

[0079] As used herein, the terms "prevent," "preventing," "prevention," "prophylactic treatment," and the like refer to reducing the likelihood of a disorder or condition occurring in a subject who does not have the disorder or condition but who is at risk of developing the disorder or condition, who is susceptible to the disorder or condition, or who is predisposed to the disorder or condition.

[0080] As used herein, the term "pseudotyped" refers to a viral vector containing one or more foreign viral structural proteins, such as envelope glycoproteins. Pseudotyped viruses can be derived from viruses in which the envelope glycoproteins of enveloped viruses or the capsid proteins of non-enveloped viruses are derived from a different virus than the source of the original viral genome and genome replication apparatus (D.A. Sanders, 2002, Curr. Opin. Biotechnol., 13:437-442). The foreign viral envelope proteins of pseudotyped viruses can be used to alter host tropism or increase or decrease viral particle stability. Examples of pseudotyped viral vectors include viruses containing one or more envelope glycoproteins that do not naturally occur on the outside of wild-type viruses. Pseudotyped viral vectors can infect cells and express and produce proteins or molecules encoded by polynucleotides contained within the viral vector, such as reporter or effector proteins or molecules, e.g., the sodium channel Nav1.1 encoded by the SCN1A gene.

[0081] As used herein, the term "recombinant," in the context of a protein or nucleic acid, refers to a protein or nucleic acid that does not occur in nature (or in a naturally occurring protein or nucleic acid sequence), but is the product of bioengineering, often or typically the product of utilizing molecular biological or molecular genetic tools and techniques practiced by those of skill in the art. For example, in some embodiments, a recombinant protein or nucleic acid molecule comprises an amino acid or nucleotide sequence that contains at least one, at least two, at least three, at least four, at least five, at least six, at least seven, or at least eight mutations compared to any naturally occurring sequence.

[0082] By "reduce" is meant to negatively alter by at least 5%, 10%, 25%, 50%, 75%, or 100%.

[0083] "Reference" refers to a standard or control condition. A "reference sequence" is a defined sequence used as a basis for sequence comparison. A reference sequence can be a portion or the entirety of a specified sequence, for example, a full-length cDNA or gene sequence, or a portion of a complete cDNA or gene sequence. For polypeptides, the length of a reference polypeptide sequence is generally at least about 16 amino acids, at least about 20 amino acids, at least about 25 amino acids, or about 35 amino acids, about 50 amino acids, or about 100 amino acids. For nucleic acids, the length of a reference nucleic acid sequence is generally at least about 50 nucleotides, at least about 60 nucleotides, at least about 75 nucleotides, or about 100 nucleotides, or about 300 nucleotides, or any integer close thereto or therebetween.

[0084] By "specifically binds" is meant a nucleic acid molecule, polypeptide, or complex thereof (e.g., a binding protein, e.g., a transcription factor and its cognate nucleic acid binding region), or compound, or molecule that recognizes and binds a given polypeptide and / or nucleic acid molecule, but does not substantially recognize and bind other molecules present in a sample, e.g., a biological sample.

[0085] By "subject" is meant a mammal, including but not limited to a human or non-human mammal, such as a non-human primate, e.g., a marmoset, or a non-human mammal, e.g., a bovine, equine, canine, ovine, or feline mammal, or a sheep, goat, llama, camel, or rodent (rat, mouse), ferret, gerbil, hamster, or zebrafinch. A subject is typically a patient, e.g., a human patient, undergoing treatment for a particular disease or condition described herein (e.g., a neuropsychiatric, neurological, or neurodevelopmental disease, disorder, or condition, e.g., seizures, epilepsy, or DS). Examples of subjects and patients include mammals, e.g., humans, undergoing treatment for such a disease or condition or at risk of having such a disease or condition.

[0086] Ranges provided herein are understood to be shorthand for all values within that range. For example, a range of 1 to 50 is understood to include any number, combination of numbers, or subrange from the group consisting of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50, inclusive of the first and last values.

[0087] As used herein, the term "therapeutically effective amount" refers to an amount of a therapeutic agent that, when administered to a patient in need of treatment, is sufficient to treat, alleviate, reduce, diagnose, prevent, and / or delay the onset of one or more symptoms of a disease, disorder, and / or condition. In some cases, a therapeutically effective amount may also refer to an amount of a therapeutic agent administered prophylactically (e.g., prior to the onset of the most severe disease) to a subject at risk of developing a disease or its symptoms, such as a neurological, neurodegenerative, or neurodevelopmental disease or disorder. In one embodiment, the disorder is Dravet syndrome (DS).

[0088] As used herein, the terms "treat," "treating," "treatment," and the like refer to reducing or ameliorating a disorder and / or its associated symptoms. It is understood, although not excluded, that treatment of a disorder or condition does not require the complete elimination of the disorder, condition, or its associated symptoms. "Treat" or "treatment" can refer to therapeutic treatment, the purpose of which is to prevent or slow (alleviate or reduce) an undesirable physiological change or disorder. Beneficial or desired clinical results include, but are not limited to, alleviation of symptoms, whether detectable or undetectable, reduction in the extent of the disease, stabilization of the disease state (i.e., no worsening), delay or slowing of disease progression, remission or palliation of the disease state, and relief (whether partial or complete). Subjects in need of treatment include those already with the condition or disorder, as well as those susceptible to the condition or disorder, or those in whom the condition or disorder is to be prevented.

[0089] As used herein, the terms "prevent," "preventing," "prevention," "prophylactic treatment," and the like refer to inhibiting or blocking the full development of a disease state or disease in a subject, or reducing the likelihood of a disease, disorder, or condition occurring in a subject who does not have the disease, disorder, or condition but who is at risk of developing the disease, disorder, or condition or who is susceptible to developing the disease, disorder, or condition.

[0090] As used herein, the term "vector" refers to a nucleic acid (e.g., a DNA vector, e.g., a plasmid), an RNA vector, a virus, or other suitable replicon (e.g., a viral vector). "Vector" also refers to a nucleic acid (polynucleotide) molecule into which a foreign nucleic acid can be inserted without destroying the vector's ability to express, replicate, and / or integrate in a host cell. Various vectors have been developed to deliver polynucleotides encoding exogenous proteins into prokaryotic or eukaryotic cells. A vector may contain a polynucleotide sequence containing a gene of interest (e.g., a transgene, e.g., a therapeutic gene, a reporter gene, or more specifically, the SCN1A gene encoding the Nav1.1 sodium channel), as well as additional sequence elements that can, for example, regulate the transcription, translation, and / or integration of these polynucleotide sequences into a cellular genome. A vector may contain regulatory sequences, such as a promoter, e.g., a subgenomic promoter, a region that induces gene transcription, and an enhancer region. The vector may contain a polynucleotide sequence (enhancer sequence) that increases the translation rate of these genes or improves the stability or nuclear export of mRNA resulting from gene transcription.These sequence elements may include, for example, 5' untranslated region and 3' untranslated region, internal ribosome entry site (IRES), and / or polyadenylation signal site to induce efficient transcription of the gene carried on the expression vector.Vector, for example, the viral vector or rAAV vector described herein, may also be called an expression vector.

[0091] " Transduction " refers to the process in which the DNA or polynucleotide contained in a virus or viral vector, for example, one or more transgenes, is introduced or transferred into a cell by the virus or viral vector, and the DNA or polynucleotide is expressed.In one embodiment, the DNA or polynucleotide transduced into a cell by a viral vector, for example, the rAAV vector described herein, is stably expressed in the cell.In some cases, the virus or viral vector is said to infect the cell.

[0092] As used herein, the term "vehicle" refers to the solvent, diluent, or carrier component of a pharmaceutical composition.

[0093] "Virus particle" (also called virion) refers to a virus (infectious agent) that exists as an independent particle containing the core viral genome or genetic material (RNA or DNA), a protein coat called a capsid that surrounds and protects the genetic material, and, in some cases, a lipid envelope surrounding the capsid. A virus particle may refer to the form of a virus before it infects and is taken up by a cell, or it may refer to the form of a virus that has infected a cell.

[0094] "Virus-like particle (VLP)" refers to a viral particle composed of one or more viral structural proteins but lacking the viral genome. Because VLPs lack the viral genome, they are non-infectious, resulting in safer and potentially more economical vaccines and vaccine products. Furthermore, VLPs can often be produced by heterologous expression and are easily purified. Most VLPs contain at least the viral core protein, which drives the budding and release of the particle from the host cell.

[0095] "Substantially identical" refers to a polypeptide or nucleic acid molecule that exhibits at least 50% identity to a reference amino acid sequence (e.g., any one of the amino acid sequences described herein) or nucleic acid sequence (e.g., any one of the nucleic acid sequences described herein). Preferably, such a sequence is at least 60% identical, preferably at least 70% identical, more preferably 80% or 85% identical, and most preferably 90%, 95%, or even 99% identical at the amino acid level or nucleic acid level, e.g., over a specified comparison window. Optimal alignment can be performed using the homology alignment algorithm of Needleman and Wunsch, 1970, J. Mol. Biol., 48:443. Substantial identity between two peptide or polypeptide sequences indicates that one peptide or polypeptide is immunologically reactive with a specific antibody raised against the other peptide or polypeptide, although such cross-reactivity is not required for two polypeptides to be considered substantially identical. Thus, for example, a peptide or polypeptide is substantially identical to another peptide or polypeptide if the two peptides or polypeptides differ only by conservative substitutions. "Substantially similar" peptides or polypeptides share sequences as described above, except that residue positions that are not identical may differ only by conservative amino acid changes. Conservative substitutions typically include, but are not limited to, substitutions within the following groups: glycine and alanine; valine, isoleucine, and leucine; aspartic acid and glutamic acid; asparagine and glutamine; serine and threonine; lysine and arginine; and phenylalanine and tyrosine, as well as others known to those skilled in the art.

[0096] Sequence identity is typically measured using sequence analysis software (e.g., Sequence Analysis Software Package of the Genetics Computer Group, University of Wisconsin Biotechnology Center, 1710 University Avenue, Madison, Wis. 53705, BLAST, BESTFIT, GAP, or PILEUP / PRETTYBOX programs). Such software matches identical or similar sequences by assigning degrees of homology to various substitutions, deletions, and / or other modifications. Conservative substitutions typically include substitutions within the following groups: glycine, alanine; valine, isoleucine, leucine; aspartic acid, glutamic acid, asparagine, glutamine; serine, threonine; lysine, arginine; and phenylalanine, tyrosine. In an exemplary approach to determining the degree of identity, e, which indicates closely related sequences, is used. -3 ~e -100 The BLAST program may be used with a probability score of

[0097] "Substantially identical" generally refers to a polypeptide or nucleic acid molecule that exhibits at least 50% identity to a reference amino acid sequence (e.g., any one of the amino acid sequences described herein) or nucleic acid sequence (e.g., any one of the nucleic acid sequences described herein). In embodiments, such a sequence is at least 60%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or more identical, or at least 99% identical at the amino acid or nucleic acid level to the sequence used for comparison.

[0098] Polynucleotides or viral nucleic acid molecules useful in the methods and compositions described herein include any nucleic acid molecule encoding a polypeptide or fragment thereof or encoding a component of a viral vector described herein. The polynucleotide or viral nucleic acid molecule may encode a polypeptide product contained in the viral vector, such as a recombinant adeno-associated virus (rAAV), as well as a peptide or fragment thereof. Such nucleic acid molecules do not need to be 100% identical to the endogenous sequence or viral vector nucleic acid sequence, but typically exhibit substantial identity. Polynucleotides that have substantial identity to the endogenous sequence or viral vector sequence typically can hybridize to at least one strand of a double-stranded nucleic acid molecule or to the viral vector nucleic acid molecule. Nucleic acid molecules useful in the described methods include any nucleic acid molecule encoding a polypeptide or fragment thereof described herein. "Hybridize" means pairing under various stringency conditions, i.e., nucleic acid molecules forming double-stranded molecules between complementary polynucleotide sequences (e.g., genes or nucleic acid sequences described herein) or portions thereof (see, e.g., Wahl, GM and SL Berger (1987) Methods Enzymol. 152:399; Kimmel, AR (1987) Methods Enzymol. 152:507).

[0099] For example, stringent salt concentrations are typically less than about 750 mM NaCl and 75 mM trisodium citrate, preferably less than about 500 mM NaCl and 50 mM trisodium citrate, and more preferably less than about 250 mM NaCl and 25 mM trisodium citrate. Low stringency hybridization can be achieved in the absence of organic solvents, such as formamide, whereas high stringency hybridization can be achieved in the presence of at least about 35% formamide, more preferably at least about 50% formamide. Stringent temperature conditions typically include a temperature of at least about 30°C, more preferably at least about 37°C, and most preferably at least about 42°C. Various additional parameters, such as hybridization time, the concentration of detergents, e.g., sodium dodecyl sulfate (SDS), and the use or non-use of carrier DNA, are well known to those skilled in the art. Various stringency levels can be achieved by combining these various conditions as needed. In one embodiment, hybridization is performed at 30° C. in 750 mM NaCl, 75 mM trisodium citrate, and 1% SDS. In a more preferred embodiment, hybridization is performed at 37° C. in 500 mM NaCl, 50 mM trisodium citrate, 1% SDS, 35% formamide, and 100 μg / ml denatured salmon sperm DNA (ssDNA). In another embodiment, hybridization is performed at 42° C. in 250 mM NaCl, 25 mM trisodium citrate, 1% SDS, 50% formamide, and 200 μg / ml ssDNA. Useful variations of these conditions will be readily apparent to those of skill in the art.

[0100] For most applications, wash steps following hybridization also vary in stringency. Wash stringency conditions can be defined by salt concentration and temperature. As noted above, wash stringency can be increased by decreasing salt concentration or increasing temperature. For example, stringent salt concentrations for wash steps are preferably less than about 30 mM NaCl and 3 mM trisodium citrate, and most preferably less than about 15 mM NaCl and 1.5 mM trisodium citrate. Stringent temperature conditions for wash steps typically include temperatures of at least about 25°C, more preferably at least about 42°C, and even more preferably at least about 68°C. In one embodiment, wash steps are performed at 25°C in 30 mM NaCl, 3 mM trisodium citrate, and 0.1% SDS. In another embodiment, wash steps are performed at 42°C in 15 mM NaCl, 1.5 mM trisodium citrate, and 0.1% SDS. In yet another embodiment, the washing step is carried out at 68°C in 15 mM NaCl, 1.5 mM trisodium citrate, and 0.1% SDS. Further variations of these conditions will be readily apparent to those skilled in the art. Hybridization techniques are well known to those skilled in the art and are described, for example, in Benton and Davis (Science 196:180, 1977); Grunstein and Hogness (Proc. Natl. Acad. Sci., USA 72:3961, 1975); Ausubel et al. (Current Protocols in Molecular Biology, Wiley Interscience, New York, 2001); Berger and Kimmel (Guide to Molecular Cloning Techniques, 1987, Academic Press, New York); and Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, New York.

[0101] Nucleic acids that do not hybridize to each other under stringent conditions are still substantially identical if the polypeptides they encode are substantially identical. This occurs, for example, when a single copy of a nucleic acid is created using the maximum codon degeneracy permitted by the genetic code. In such cases, the nucleic acids typically hybridize under moderately stringent hybridization conditions. Non-limiting examples of "moderately stringent hybridization conditions" include hybridization at 37°C in a buffer containing 40% formamide, 1M NaCl, and 1% SDS, followed by a wash in 1xSSC at 45°C. Positive hybridization is at least twice the background level. Those skilled in the art will readily recognize that alternative hybridization and wash conditions can be used to achieve similar stringency conditions.

[0102] "Ortholog" refers to any polypeptide or nucleic acid molecule of one organism that is highly related to a reference protein or nucleic acid sequence from another organism. The degree of relatedness may be expressed as the likelihood that the reference protein will identify the sequence in, for example, a BLAST search. The likelihood that a reference sequence will identify a random sequence as an ortholog is extremely low, e.g. -10 , e -20 , e -30 , e -40 , e -50 , e -75 , e -100 Those skilled in the art will understand that an ortholog is likely to be functionally related to the reference protein or nucleic acid sequence. In other words, an ortholog and its reference molecule, for example, a mouse ortholog and a human ortholog, are expected to play similar, if not identical, functional roles in the respective organisms.

[0103] Orthologs are not required to share a particular degree of amino acid sequence identity with a reference sequence when aligned with the reference sequence. Protein orthologs may share significant amino acid sequence identity across the entire length of the protein, for example, or alternatively across only one functionally important domain of the protein. Such functionally important domains may be defined by genetic mutation or by structure-function assays. Orthologs can be identified using methods practiced in the art. The functional role of orthologs can be assayed using methods well known to those skilled in the art. For example, function may be assayed in vivo or in vitro using biochemical, immunological, or enzymatic assays; or transformation rescue. Alternatively, bioassays may be performed in tissue culture. Function may also be assayed by gene inactivation (e.g., by RNAi, siRNA, or gene knockout), gene overexpression, and other methods.

[0104] Ranges provided herein are understood to be shorthand for all values within that range. For example, a range of 1 to 50 is understood to include any number, combination of numbers, or subrange from the group consisting of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50, inclusive of the first and last values.

[0105] By SCN1A is meant a polypeptide or protein (sodium channel Nav1.1) or fragments thereof having at least about 85% or 85% or at least about 90%, about 95%, about 98%, about 99% or 90%, 95%, 98%, 99% or more amino acid sequence identity to the amino acid sequence of the classical amino acid sequence of SCN1A, human isoform 1, OmniProt identification number P35498-1 (length 2,009 amino acids; mass (Da): 228,972); RefSeq numbers NP_001159435.1; NP_001189364.1; NP_001340877). The polypeptide (protein) sequence of human SCN1A is as follows: TIFF2025118768000001.tif205138TIFF2025118768000002.tif182138

[0106] The Nav1.1 sodium channel is encoded by a human SCN1A polynucleotide sequence or fragment thereof having at least about 85%, or 85%, or at least about 90%, or about 95%, or about 98%, or about 99%, or 90%, 95%, 98%, 99%, or more sequence identity to the SCN1A polynucleotide sequence of accession number NCBI CCDS 54413.1 (RefSeq numbers NM_001165963.2; NM_001202435.2; NM_001353948.1), as set forth below (genomic information from Genome Reference Consortium GRCh38.p12; GenBank assembly accession: GCA_000001405.27 (latest); RefSeq assembly accession: GCF_000001405.38 (latest)).

[0107] SCN1A nucleotide sequence (6030 nt): TIFF2025118768000003.tif211146TIFF2025118768000004.tif140146

[0108] The sodium channel Nav1.1, encoded by the SCN1A gene, is expressed in three distinct neuronal populations in the cortex, including parvalbumin-expressing fast-spiking cortical interneurons (PV cINs), vasoactive intestinal peptide-expressing dis-inhibitory cortical interneurons (VIP cINs), and layer 5 pyramidal neurons.

[0109] The amino acid sequence of the unmodified human muscarinic acetylcholine receptor M3 is provided in the NCBI reference sequence NP_000731.1 as shown below. Also encompassed are polypeptides or proteins or functional fragments thereof having at least about 85% or 85%, or at least about 90%, about 95%, about 98%, about 99% or 90%, 95%, 98%, 99% or more sequence identity to TIFF2025118768000005.tif45146.

[0110] The amino acid sequence of the human Gq-DREADD (hM3Dq) excitatory receptor is derived from the amino acid sequence of the unmodified human muscarinic acetylcholine receptor M3 shown above, as follows: As shown in TIFF2025118768000006.tif216147, in the Gq-DREADD (hM3Dq) receptor amino acid sequence (590 aa), the tyrosine at position 149 has been replaced by a cysteine, and the arginine at position 239 has been replaced by a glycine (U.S. Patent Application Publication No. 2018 / 0078658).

[0111] As used herein, the term "or" is understood to be inclusive unless specifically stated otherwise or clear from context. As used herein, the terms "a," "an," and "the" are understood to be singular or plural unless specifically stated otherwise or clear from context.

[0112] As used herein, the term "about" or "approximately" means within an acceptable error range for the type of value being described and the method used to measure that value. For example, these terms can indicate within 20%, more preferably within 10%, and most preferably even within 5% of a given value or range. More specifically, "about" can be understood to mean within 20%, 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2%, 1%, 0.5%, 0.1%, 0.05%, or 0.01% of a stated value or range. Alternatively, particularly in biological systems, the term "about" can mean within one log unit (i.e., one order of magnitude), preferably within half, of a given value. Unless specifically stated or clear from the context, the term "about" as used herein is understood to mean within normal tolerances in the art, e.g., within two standard deviations of the mean. Unless clear from the context, all numerical values provided herein are modified by the term about.

[0113] The recitation of a list of chemical or moiety groups in any definition of a variable herein includes defining that variable as any one group or combination of listed groups. The recitation of an embodiment of a variable or aspect herein includes that embodiment as any one embodiment or in combination with any other embodiment or portion thereof as described in this disclosure.

[0114] Any composition or method provided herein can be combined with any one or more of the other compositions and methods provided herein. [The present invention 1001] A viral vector comprising a transgene polynucleotide sequence and an enhancer polynucleotide sequence that specifically restricts expression of the transgene to parvalbumin (PV)-expressing interneuron cells in the brain. [The present invention 1002] A viral vector comprising an enhancer polynucleotide sequence specifically associated with SCN1A gene expression and a transgene polynucleotide sequence, wherein the enhancer sequence restricts expression of the transgene to PV-expressing interneuron cells in the brain. [The present invention 1003] The viral vector of the present invention 1001 or 1002, wherein the transgene is a reporter gene, a designer receptor exclusively activated by designer drugs (DREADD)-encoding gene, a pharmacologically selective actuator molecule (PSAM)-encoding therapeutic gene, or a therapeutic gene. [The present invention 1004] The viral vector of any one of 1001 to 1003, wherein the transgene is an SCN1A gene. [The present invention 1005] The viral vector of any one of 1001 to 1003, wherein the transgene is a DREADD-encoding gene. [The present invention 1006] 1005. The viral vector of the present invention, wherein the DREADD-encoding gene is a Gq-DREADD-encoding gene that is activated by the chemogen clozapine-N4-oxide (CNO). [The present invention 1007] 1003. The viral vector of the present invention, wherein the transgene is a pharmacologically selective actuator molecule (PSAM)-encoding therapeutic gene. [The present invention 1008] The viral vector of any one of claims 1001 to 1007, which is a recombinant adeno-associated virus (rAAV) vector. [The present invention 1009] A recombinant adeno-associated virus (rAAV) vector comprising an SCN1A transgene polynucleotide sequence or a functional portion thereof and an enhancer polynucleotide sequence that specifically restricts expression of the SCN1A transgene to interneurons or neuronal cells of the brain. [The present invention 1010] The rAAV vector of the present invention 1004 or 1009, wherein the Nav1.1 sodium channel encoded by the SCN1A transgene is functionally expressed in interneuron cells after transduction of the interneuron cells with the rAAV vector. [The present invention 1011] The viral vector or rAAV vector of any one of 1001 to 1010, wherein the interneuron cell is a GABAergic interneuron cell. [The present invention 1012] 1009. The rAAV vector of the present invention, wherein the interneuron cells are GABAergic interneuron cells in the telencephalon of the brain. [The present invention 1013] 1011. The rAAV vector of the present invention, wherein GABAergic interneuron cells express parvalbumin (PV). [The present invention 1014] The rAAV vector of any one of 1009 to 1011, wherein GABAergic interneuron cells express vasoactive intestinal peptide (VIP). [The present invention 1015] The rAAV vector of any one of 1009 to 1011, wherein the neuronal cell is a pyramidal (PYR) neuron of the cerebral cortex. [The present invention 1016] The viral vector or rAAV vector of any of claims 1001 to 1013, wherein the enhancer polynucleotide sequence comprises a nucleotide sequence containing one or more regions of about 100 bp or more that have at least 75% or more sequence identity to the polynucleotide sequence of human enhancer element E1, E2, E3, E4, E7, E8, E9, or E10 (SEQ ID NOs: 15 to 18 or 21 to 24, respectively). [The present invention 1017] Any of the viral vectors or rAAV vectors of claims 1001 to 1013, wherein the enhancer polynucleotide sequence comprises the polynucleotide sequence of human enhancer element E1, E2, E3, E4, E7, E8, E9, or E10 (SEQ ID NO: 15 to 18 or 21 to 24, respectively). [The present invention 1018] A viral vector or rAAV vector of the present invention, wherein the enhancer polynucleotide sequence comprises a nucleotide sequence containing one or more regions of about 100 bp or more that have at least 75% or more sequence identity to the polynucleotide sequence of human enhancer element E2 (SEQ ID NO:16). [The present invention 1019] The rAAV vector of the present invention 1014 or 1015, wherein the enhancer polynucleotide sequence comprises a nucleotide sequence containing one or more regions of about 100 bp or more that have at least 75% or more sequence identity to the polynucleotide sequence of human enhancer element E6 (SEQ ID NO:20) or human enhancer element E5 (SEQ ID NO:19). [The present invention 1020] The rAAV vector of the present invention, wherein the enhancer polynucleotide sequence comprises the polynucleotide sequence of human enhancer element E6 (SEQ ID NO:20) or the polynucleotide sequence of human enhancer element E5 (SEQ ID NO:19). [The present invention 1021] The viral vector or rAAV vector of any of claims 1001 to 1020, wherein the capacity of the vector to package polynucleotide sequences greater than about 4.7 kb includes reassortment of multiple rAAV vectors by homologous recombination or reassortment of multiple rAAV vectors by acceptor site-mediated splicing. [The present invention 1022] The viral vector or rAAV vector of any of claims 1004 or 1009 to 1020, wherein the vector delivers the SCN1A gene to SCN1A-expressing GABAergic interneuron cells in the brain, and the SCN1A gene is functionally expressed, thereby restoring normal levels of SCN1A in the interneuron cells after administration of the vector to a subject. [The present invention 1023] The viral vector or rAAV vector of the present invention 1022, wherein the subject is a human patient. [The present invention 1024] The viral vector or rAAV vector of the present invention 1023, wherein the human patient is an infant suffering from Dravet syndrome (DS). [The present invention 1025] A virus particle or virus-like particle comprising the virus vector or rAAV vector of any one of the present inventions 1001 to 1024. [The present invention 1026] A cell comprising the viral vector or rAAV vector of any one of the present inventions 1001 to 1024. [The present invention 1027] A cell comprising a virus particle or virus-like particle of the present invention. [The present invention 1028] A pharmaceutical composition comprising any one of the viral vectors or rAAV vectors of the present inventions 1001 to 1024 and a pharmaceutically acceptable vehicle, carrier, or diluent. [The present invention 1029] A pharmaceutical composition comprising a virus or virus-like particle of the present invention 1025 and a pharmaceutically acceptable vehicle, carrier, or diluent. [The present invention 1030] The pharmaceutical composition of invention 1028 or invention 1029, which is in a liquid dosage form. [The present invention 1031] A method for restoring normal levels of SCN1A expression in GABAergic interneuron cells or neuronal cells that are deficient or defective in SCN1A expression levels, comprising the step of contacting the cells with an effective amount of any of the viral vectors or rAAV vectors of the present invention 1004 or 1009 to 1022, viral particles thereof, or pharmaceutical compositions thereof, thereby restoring normal levels of SCN1A expression in the GABAergic interneuron cells or neuronal cells. [The present invention 1032] A method for treating infantile epilepsy and / or seizures in an infant having epilepsy, seizures, or Dravet syndrome (DS) or at risk of having epilepsy, seizures, or Dravet syndrome (DS), comprising administering to the infant a therapeutically effective amount of a viral vector or rAAV vector of any of inventions 1001 to 1024, a viral particle or virus-like particle of invention 1025, or a pharmaceutical composition of any of inventions 1028 to 1030, to treat the seizures, epilepsy, or DS in the subject. [The present invention 1033] A method for treating Dravet syndrome (DS) in a subject having or at risk of having Dravet syndrome (DS), comprising administering to the subject a therapeutically effective amount of any one of the viral vectors or rAAV vectors, viral particles thereof, or pharmaceutical compositions of the present invention 1004 or 1009 to 1022, thereby treating DS in the subject. [The present invention 1034] A method for inhibiting or preventing seizures and / or epilepsy in a subject having or at risk of having seizures and / or epilepsy, comprising systemically administering to the subject a recombinant adeno-associated virus (rAAV) vector comprising an SCN1A transgene polynucleotide sequence or a functional portion thereof, an enhancer polynucleotide sequence that specifically restricts expression of the SCN1A transgene to interneuronal or neuronal cells of the subject's cerebral cortex, and a capsid that enhances transduction of the vector into interneuronal cells. [This invention 1035] The method of any of claims 1032 to 1034, wherein the infant or subject is a human patient. [The present invention 1036] Any of the methods of claims 1031 to 1035, wherein the enhancer polynucleotide sequence in the rAAV vector comprises one or more regions of about 100 bp or more that have at least 75% or more sequence identity to the polynucleotide sequence of human enhancer element E1, E2, E3, E4, E5, E6, E7, E8, E9, or E10 (SEQ ID NOs: 15 to 24, respectively). [This invention 1037] The method of claim 1036, wherein the enhancer polynucleotide sequence in the rAAV vector comprises one or more regions of about 100 bp or more that have at least 75% or more sequence identity to the polynucleotide sequence of human enhancer element E2 (SEQ ID NO:16). [The present invention 1038] 1037. The method of claim 1037, wherein the enhancer polynucleotide sequence is the human enhancer element E2 polynucleotide sequence of SEQ ID NO:16. [This invention 1039] The method of claim 1036, wherein the enhancer polynucleotide sequence in the rAAV vector comprises one or more regions of about 100 bp or more that have at least 75% or more sequence identity to the polynucleotide sequence of human enhancer element E6 (SEQ ID NO:20) or the polynucleotide sequence of human enhancer element E5 (SEQ ID NO:19). [The present invention 1040] 1039. The method of claim 1039, wherein the enhancer polynucleotide sequence is the human enhancer element E6 polynucleotide sequence of SEQ ID NO:20 or the human enhancer element E5 polynucleotide sequence of SEQ ID NO:19. [This invention 1041] A method for delivering a transgene for restricted expression in interneuronal or neuronal cells expressing the SCN1A gene to inhibit or prevent seizures and / or epilepsy in a subject in need thereof, the method comprising contacting the cells with a recombinant adeno-associated virus (rAAV) vector comprising an SCN1A transgene polynucleotide sequence or a functional portion thereof and an enhancer polynucleotide sequence that specifically restricts expression of the SCN1A transgene to interneuronal or neuronal cells of the subject's cerebral cortex, thereby inhibiting or preventing seizures and / or epilepsy in the subject. [The present invention 1042] The method of any of claims 1031 or 1034 to 1041, wherein the interneuron cell is selected from a PV-expressing cortical interneuron (PV-cIN), a vasoactive intestinal peptide-expressing disinhibited cortical interneuron (VIP cIN), or a pyramidal neuron. [This invention 1043] The method of claim 1041 or 1042, wherein the enhancer polynucleotide sequence in the rAAV vector comprises one or more regions of about 100 bp or more that have at least 75% or more sequence identity to the polynucleotide sequence of human enhancer element E1, E2, E3, E4, E5, E6, E7, E8, E9, or E10 (SEQ ID NOs: 15 to 24, respectively). [This invention 1044] The enhancer polynucleotide sequence in the rAAV vector is Polynucleotide sequence of human enhancer element E2 (SEQ ID NO: 16); the polynucleotide sequence of human enhancer element E6 (SEQ ID NO:20), or Polynucleotide sequence of human enhancer element E5 (SEQ ID NO:19) The method of the present invention 1041 or 1042, comprising one or more regions of about 100 bp or more having at least 75% or more sequence identity with [This invention 1045] The method of claim 1041 or claim 1042, wherein the enhancer polynucleotide sequence in the rAAV vector is selected from human enhancer elements E1, E2, E3, E4, E5, E6, E7, E8, E9, or E10 (SEQ ID NOs: 15 to 24, respectively). [The present invention 1046] The method of claim 1045, wherein the enhancer polynucleotide sequence is the human enhancer element E2 polynucleotide sequence of SEQ ID NO:16, the human enhancer element E6 (SEQ ID NO:20), or the human enhancer element E5 (SEQ ID NO:19). [This invention 1047] The method of any of claims 1032 to 1046, wherein the rAAV vector, virus particle, virus-like particle, or pharmaceutical composition is administered systemically. [This invention 1048] The method of any of claims 1032 to 1046, wherein the rAAV vector, viral particle, or pharmaceutical composition is administered parenterally. [This invention 1049] The method of claim 1047 or claim 1048, wherein the rAAV vector, virus particle, virus-like particle, or pharmaceutical composition is administered intravenously. [The present invention 1050] The method of any of claims 1032 to 1046, wherein the rAAV vector, virus particle, virus-like particle, or pharmaceutical composition is administered intracerebrally. [This invention 1051] The method of any of claims 1032 to 1050, wherein the rAAV vector, virus particle, virus-like particle, or pharmaceutical composition is administered as a prophylactic. [This invention 1052] The method of any of claims 1032 to 1051, further comprising administering adjunctive anti-epileptic treatment to the infant or subject. [This invention 1053] A viral vector comprising a transgene polynucleotide sequence and an enhancer polynucleotide sequence that specifically restricts expression of the transgene to vasoactive intestinal peptide-expressing cortical interneuron cells (VIP cINs) in the brain. [This invention 1054] A viral vector comprising an enhancer polynucleotide sequence specifically associated with SCN1A gene expression and a transgene polynucleotide sequence, wherein the enhancer sequence restricts expression of the transgene to vasoactive intestinal peptide-expressing cortical interneuron cells (VIP cINs) in the brain. [This invention 1055] The viral vector of the present invention 1053 or 1054, wherein the enhancer polynucleotide sequence comprises a nucleotide sequence containing one or more regions of about 100 bp or more having at least 75% or more sequence identity with the polynucleotide sequence of human enhancer element E6 (SEQ ID NO:20). [This invention 1056] The viral vector of any one of 1053 to 1055, wherein the enhancer polynucleotide sequence is human enhancer element E6 (SEQ ID NO: 20). [This invention 1057] A viral vector comprising a transgene polynucleotide sequence and an enhancer polynucleotide sequence that specifically restricts expression of the transgene to pyramidal neurons of the brain. [This invention 1058] A viral vector comprising an enhancer polynucleotide sequence specifically associated with SCN1A gene expression and a transgene polynucleotide sequence, wherein the enhancer sequence restricts expression of the transgene to pyramidal neurons in the brain. [This invention 1059] The viral vector of the present invention 1057 or 1058, wherein the enhancer polynucleotide sequence comprises a nucleotide sequence containing one or more regions of about 100 bp or more having at least 75% or more sequence identity with the polynucleotide sequence of human enhancer element E5 (SEQ ID NO:19). [The present invention 1060] The viral vector of any one of 1057 to 1059, wherein the enhancer polynucleotide sequence is human enhancer element E5 (SEQ ID NO: 19). [This invention 1061] The viral vector of any one of 1058 to 1060, wherein the enhancer sequence restricts expression of the transgene to glutamatergic pyramidal neurons in the brain. [This invention 1062] The viral vector of any one of claims 1058 to 1061, wherein the enhancer sequence restricts expression of the transgene to pyramidal neurons in cortical layer 5 of the brain. [This invention 1063] The viral vector of any one of 1053 to 1062 of the present invention, which is a lentiviral vector or a recombinant adeno-associated viral (rAAV) vector. [This invention 1064] The viral vector of any one of 1053 to 1063 of the present invention, wherein the transgene is an SCN1A gene. [This invention 1065] A viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NOs: 15 to 24 or a functional part thereof, which specifically targets SCN1A-expressing neuronal cells. [The present invention 1066] 1065. The viral vector of the present invention, wherein the neuronal cells are parvalbumin cortical interneurons (PV cINs), pyramidal (PYR) neurons, or vasoactive intestinal peptide cortical interneurons (VIP cINs). [This invention 1067] A viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NOs: 25 to 27 or a functional part thereof, which specifically targets Pvalb-expressing cells. [The present invention 1068] A viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NOs: 28 to 31 or a functional part thereof, which specifically targets Acan-expressing cells. [The present invention 1069] A viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NOs: 32 to 39 or a functional portion thereof, which specifically targets Tmem132c-expressing cells. [The present invention 1070] A viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NO: 40 or SEQ ID NO: 41, or a functional part thereof, which specifically targets Lrrc38-expressing cells. [This invention 1071] A viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NO: 42 or SEQ ID NO: 43, or a functional part thereof, which specifically targets Inpp5j-expressing cells. [This invention 1072] A viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NOs: 44 to 47 or a functional part thereof, which specifically targets Mef2c-expressing cells. [This invention 1073] A viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NO:48 or SEQ ID NO:49 or a functional portion thereof, which specifically targets Pthlh-expressing cells. [This invention 1074] A viral vector comprising an enhancer polynucleotide sequence selected from SEQ ID NOs: 15 to 49 or a functional part thereof, which specifically targets PV-expressing cells. [This invention 1075] The viral vector of any one of claims 1065 and 1067 to 1074, wherein the target cell is a PV-expressing neuronal cell. [This invention 1076] The viral vector of any one of 1065 to 1075 of the present invention, which is a recombinant adeno-associated virus (rAAV) vector. [This invention 1077] A virus particle or virus-like particle comprising the virus vector of any one of 1065 to 1076 of the present invention. [This invention 1078] A cell comprising any one of the viral vectors of the present inventions 1065 to 1076. [This invention 1079] A cell comprising the virus particle or virus-like particle of the present invention. [The present invention 1080] A pharmaceutical composition comprising the viral vector of any one of the present inventions 1065 to 1076 or the virus particle or virus-like particle of the present invention 1077, and a pharmaceutically acceptable vehicle, carrier, or diluent. [This invention 1081] A method for restricting expression of a transgene to neuronal cells of a subject, comprising administering to the subject a delivery vector comprising at least one enhancer element polynucleotide comprising a sequence of SEQ ID NO: 15-49 and a transgene polynucleotide, wherein the transgene is specifically expressed in neuronal cells. [This invention 1082] 1081. The method of claim 1081, wherein the transgene is SCN1A. [This invention 1083] The method of claim 1082, wherein the neuronal cells are parvalbumin-expressing cortical interneurons (PV cINs). [This invention 1084] The method of claim 1082 or claim 1083, wherein the enhancer element polynucleotide comprises the sequence shown in SEQ ID NO: 15-18 or SEQ ID NO: 21-24. [This invention 1085] The method of claim 1082, wherein the neuronal cells are pyramidal (PYR) cells. [The present invention 1086] The method of claim 1085, wherein the enhancer element polynucleotide comprises the sequence shown in SEQ ID NO:19. [This invention 1087] The method of claim 1082, wherein the neuronal cells are vasoactive intestinal peptide-expressing cortical interneurons (VIP cINs). [This invention 1088] The method of claim 1087, wherein the enhancer element polynucleotide comprises the sequence shown in SEQ ID NO:20. [This invention 1089] 108. The method of any of claims 1081 to 1088, wherein the delivery vector is a lentiviral vector or rAAV. [The present invention 1090] The method of claim 1089, wherein the delivery vector is administered to the brain. [This invention 1091] The method of claim 1090, wherein the delivery vector is administered locally or systemically. [This invention 1092] The method of any one of claims 1081 to 1091, wherein the subject is a mammal. [This invention 1093] The method of claim 1092, wherein the subject is a human. [This invention 1094] A viral vector comprising a human enhancer polynucleotide sequence selected from SEQ ID NOs: 15 to 49. [This invention 1095] The viral vector of the present invention is a recombinant adeno-associated virus (rAAV) vector. [This invention 1096] A virus particle or virus-like particle comprising the viral vector of the present invention 1094 or 1095. [This invention 1097] A cell comprising the viral vector of the present invention 1094 or 1095. [This invention 1098] A cell comprising a virus particle or virus-like particle of the present invention. [This invention 1099] A pharmaceutical composition comprising the viral vector of the present invention 1094 or 1095 or the virus particle or virus-like particle of the present invention 1096 and a pharmaceutically acceptable vehicle, carrier, or diluent. [Brief explanation of the drawings]

[0115] [Figure 1A-1-1]Figures 1A-1, 1A-2, 1A-3, 1B-1, 1B-2, 1C, and 1D present tabular data and information related to the discovery and identification of specific enhancer (regulatory) sequences, referred to herein as "E1-E35." Enhancers specific for SCN1A-restricted gene expression in GABAergic interneurons, such as PV-expressing interneurons, e.g., E1-E10, as well as enhancers targeting other genes listed in the table, are shown. Figure 1A-1 presents tabular data illustrating the gene, target (e.g., neuronal cell type), specificity, location (e.g., intergenic or intronic), chromosomal location, and genomic start and stop site characteristics of 35 (35) enhancer elements, referred to as E1-E35, in the mouse genome. Similarly, Figures 1A-2 and 1A-3 present tabular data illustrating the gene, target (e.g., neuronal cell type), specificity, location (e.g., intergenic or intronic), chromosomal location, and start and stop site characteristics of these 35 (35) E1-E35 enhancer elements in the human genome. By way of example, enhancer (regulatory) elements E1-E10 (also referred to herein as S5E1-S5E10) were identified near the human SCN1A gene in the mouse genome (Figure 1A-1) and human genome (Figures 1A-2 and 1A-3). In Figures 1A-1-1A-3, the polynucleotide sequences of the mouse and human enhancer elements described herein have start and stop sites in the mouse and human genomes as shown in the tables (and in the tables of Figures 15A-1, 15A-2, 16A-1, and 16A-2). The mouse and human enhancer sequences are provided via web-accessible genome information listed in the tables in Figures 1A-1 to 1A-3. Figures 1B-1 and 1B-2 show images demonstrating reporter gene expression restricted by the E1 to E10 enhancer elements in PV-expressing interneurons in the cortical layers of the brain.The images show the results of immunohistochemical (IHC) staining analysis for dTomato in brain sections after systemic in vivo injection of the pAAV-S5-E2-dTomato vector into mice, allowing for the detection of specific cells transduced by the vector. Figures 1C and 1D show graphs quantifying the degree of specificity (Figure 1C) and sensitivity (Figure 1D) of reporter gene expression in PV-expressing interneurons in the cortex. Reporter gene expression is controlled by the E1-E10 enhancer elements contained in the rAAV vector. Specificity was quantified as the percentage of cells expressing the viral reporter dTomato that coexpress the PV interneuron marker PV, as assessed by immunohistochemistry on brain sections after systemic in vivo injection of the pAAV-S5-E2-dTomato vector into mice. Sensitivity was quantified as the percentage of cells expressing the PV interneuron marker PV that co-express the viral reporter dTomato, as assessed by immunohistochemistry on brain sections after systemic in vivo injection of pAAV-S5-E2-dTomato vector into mice. Bars represent the mean + / - standard error of the mean (s.e.m.). [Figure 1A-1-2] See the description of Figure 1A-1-1. [Figure 1A-2-1] See the description of Figure 1A-1-1. [Figure 1A-2-2] See the description of Figure 1A-1-1. [Figure 1A-3-1] See the description of Figure 1A-1-1. [Figure 1A-3-2] See the description of Figure 1A-1-1. [Figure 1B-1] See the description of Figure 1A-1-1. [Figure 1B-2] See the description of Figure 1A-1-1. [Figure 1C] See the description of Figure 1A-1-1. [Figure 1D] See the description of Figure 1A-1-1. [Figure 2A]Figures 2A and 2B show images demonstrating the localization of reporter gene expression using rAAV vectors containing an E2 enhancer element sequence and a reporter transgene (e.g., d-Tomato) or effector gene (e.g., Gq-DREADD) throughout brain structures, including the cortex. Figure 2A shows images demonstrating the results of immunohistochemical (IHC) staining analysis for the dTomato reporter in brain sections (sagittal sections at the top of the figure; coronal sections at the bottom of the figure) after systemic in vivo injection of pAAV-S5-E2-dTomato vector into animals (mice), allowing for the detection of specific cells transduced by the vector. Figure 2B shows images demonstrating the results of immunohistochemical (IHC) staining analysis for the expressed dTomato reporter in brain sections after systemic in vivo injection of pAAV-S5-E2-dTomato vector into animals (mice), allowing for the detection of specific PV-expressing cells. In brain sections, reporter gene expression from the pAAV-S5-E2-dTomato vector was visualized (Figure 2B, left panel, red). Reporter gene expression from pAAV-S5-E2-Gq-DREADD-dTomato was visualized (Figure 2B, right panel, green for Gq-DREADD and red for dTomato). Detection of specific PV-expressing cells transduced by the vector was visualized (Figure 2B, left panel and Figure 2B, right panel). [Figure 2B] See legend to Figure 2A. [Figure 3A]Figures 3A-3F show schematics, plots, graphs, and confocal microscopy images related to the identification of SCN1A enhancers. Figure 3A shows a schematic of the scATAC-seq pipeline. Interneurons were collected from the visual cortex of adult Dlx6aCre::Sun1-eGFP mice. Figure 3B shows a plot of 3,500 nuclei in UMAP space. Clusters obtained from the SnapATAC pipeline were organized into four major classes of interneurons. Figure 3C shows a Venn diagram depicting the number of unique and common peaks across four interneuron populations: PV, SST, VIP, and ID2. Figure 3D shows a schematic of the enhancer selection method at the SCN1A locus, as described in the methods herein (Example 8). Figures 3E and 3F show results obtained after systemic injection of adult mice with the indicated rAAV-E[x]-dTomato vectors containing enhancer elements as described, followed by analysis 3 weeks after injection. Immunohistochemical (IHC) analysis of the reporter in the S1 cortex against the indicated markers was used to assess reporter expression intensity (Figure 3E, upper panel) and specificity of viral reporter expression for the indicated markers (all other panels). Representative fluorescent images of the indicated viral reporters in the somatosensory cortex (Figure 3F, left panel). Dashed lines indicate the limits of the anatomical structures. The scale bar represents 100 μm. Points on the graph indicate individual measurements, and the line represents the mean + / - s.e.m. [Figure 3B] See legend to Figure 3A. [Figure 3C] See legend to Figure 3A. [Figure 3D] See legend to Figure 3A. [Figure 3E] See legend to Figure 3A. [Figure 3F] See legend to Figure 3A. [Figure 4]Figures 4A-4E show images, graphs, and recording traces associated with viral targeting of PV cortical interneurons (PV cINs) in mice. Adult mice were injected systemically (Figures 4A-4B) or locally (Figure 4D) with rAAV-E2-dTomato, which expresses the reporter dTomato under the control of E2 regulatory elements, and analyzed by immunohistochemistry (IHC) or ISH for both the reporter and PV markers 3 weeks after injection. Figure 4C shows slice recordings of intrinsic properties of virally labeled neurons. Figure 4D (right panel) shows a graph illustrating the specificity of expression, expressed as the percentage of reporter-expressing cells coexpressing PV, compared with the intensity of reporter expression. Figure 4E shows images resulting from an experiment in which mice were injected locally with rAAV-E2-dTomato, which expresses the reporter dTomato under the control of E2 regulatory elements, and analyzed at the indicated developmental stages for the reporter and the indicated markers. Scale bars represent 250 μm (Figure 4A) and 50 μm (Figures 4B, 4D, 4E). Points on the graphs represent individual measurements, and lines represent the mean + / - sem. [Figure 5A]Figures 5A–5E show images, current-clamp recording traces, and graphs related to viral monitoring and manipulation of PV cortical interneurons (PCc INs) in mice. rAAV was injected locally (Figure 5A—P10 injection with rAAV-E2-SYP-dTomato; Figure 5B—P14 injection with rAAV-E2-GCaMP6f; Figures 5D and 5E—adult injection with rAAV-E2-C1V1-eYFP) or systemically (Figure 5C—adult injection with rAAV-E2-PSAM4-5HT3-LC-GFP) into the somatosensory (S1) cortex of mice. Figure 5A shows representative images of colocalization of the SYP-dTomato reporter with the synaptic marker Syt2 1 week after injection, along with corresponding quantification. Figure 5B shows the results of Ca2+ imaging during vibrissa stimulation performed 2–3 weeks after injection. In the right panel, the success rate was calculated as the percentage of ΔF / F peaks above threshold in response to vibrissa stimulation. Figure 5C shows the results of current-clamp recordings performed on brain slices 4 weeks after injection. Traces show representative cell responses at the indicated currents at baseline and after bath application of varenicline. Figure 5D shows the results of current-clamp recordings performed on brain slices 1 week after injection. While viral reporter-expressing cells were exposed to a constant 2-second laser stimulus (550 nm), voltage was recorded for 3 seconds. During laser stimulation, adjacent pyramidal cells that do not express the viral reporter were also recorded. Figure 5E illustrates in vivo single-unit analysis of neuronal activity, showing raster plots of virally infected neurons upon laser stimulation and corresponding population quantification data. The left panel shows fast-spiking neurons, and the right panel shows normally spiking excitatory neurons. Notably, due to the mosaic nature of the local viral injection, individual cell responses were bimodal. This likely reflects whether certain cells were infected or uninfected. The scale bar represents 5 μm. The center bar above the "Trial" versus "Time" graph represents laser stimulation. Points on the graph represent individual measurements, and the line represents the mean + / - sem. [Figure 5B] See legend to Figure 5A. [Figure 5C]See legend to Figure 5A. [Figure 5D] See legend to Figure 5A. [Figure 5E] See legend to Figure 5A. [Figure 6A] Figures 6A and 6B show diagrams, graphs, images, and recording traces related to viral targeting and manipulation of PV cortical interneurons (PV cINs) in primates, including humans. Figure 6A: Animals from the indicated species were injected locally (rats and macaques) or systemically (marmosets) with rAAV-E2-C1V1-eYFP or rAAV-E2-dTomato and analyzed 2–8 weeks after injection. Specificity of expression was shown as the percentage of virally labeled cells co-expressing PV. Figure 6B: Human brain tissue obtained from surgical resection was exposed to rAAV-E2-dTomato (i–iii) or rAAV-E2-C1V1-eYFP (iv) and maintained in culture for 7–14 days. The upper right panel shows the percentage of fast-spiking neurons among virally labeled cells, as assessed by electrophysiological recording of intrinsic properties. (iv) Electrophysiological current-clamp recording of virally labeled cells upon laser stimulation. Scale bar represents 25 μm. The bar above the "direct photoactivation (PV)" trace represents laser stimulation, and the arrowhead indicates a neuron co-expressing PV and the viral reporter. Points on the graph represent individual measurements, and the line represents the mean + / - sem. [Figure 6B] See legend to Figure 6A. [Figure 7] Fluorescence images of sagittal sections from adult mice systemically injected with the indicated rAAV-E[x]-dTom viral reporter vectors and analyzed 3 weeks after injection using IHC for the viral reporter. Scale bar represents 500 μm. [Figure 8A]Figures 8A-8D show images and graphs of results after systemic injection of rAAV-E2-dTomato in adult mice. Figure 8A shows slice recordings of the intrinsic properties of virally labeled neurons. The left panel shows a representative cell expressing the viral reporter. The triangular trace at the top center represents the recording pipette. Quantification indicates the indicated parameters. The darker gray points in the "Identity" graph represent cells with typical fast-spiking (FS) properties. Figure 8B shows representative slice recording traces of positive and negative fast-spiking cells (FS and nFS, respectively). The scale bar represents 20 μm. Points on the graph represent individual measurements, and the line represents the mean + / - s.e.m. Figures 8C and 8D show results after systemic injection of rAAV-E2-dTomato in adult mice and analysis 3 weeks after injection. Figure 8C: Coronal and sagittal sections were analyzed by IHC for viral reporter and PV, reporting specificity for PV across brain regions. Figure 8D: Native viral expression was analyzed from the indicated organs. Scale bars represent 100 µm (Figure 8C) and 250 µm (Figure 8D). Points on the graphs represent individual measurements, and lines represent the mean + / - s.e.m. [Figure 8B] See legend to Figure 8A. [Figure 8C] See legend to Figure 8A. [Figure 8D] See legend to Figure 8A. [Figure 9A]Figures 9A-9C show images, recording trace data, and graphs. Mice received systemic injections (Figure 9A: P14 injection with rAAV-E2-GCaMP6f) and local injections into the somatosensory cortex (Figure 9B: rAAV-E2-C1V1-eYFP; Figure 9C: rAAV-E2-GqDREADD). Figure 9A: Mice were analyzed 1 week after injection. The left panel shows a wide-field image of two representative peaks indicated by pound signs in the middle panel. The right panel shows a fluorescence image taken after GCaMP recording. Figure 9B: Slice electrophysiology current-clamp recordings were performed 1 week after injection. Voltage was recorded for 3 seconds while targeting viral reporter-expressing cells with 10 Hz or 40 Hz laser stimulation (550 nm). Figure 9C: Slice electrophysiology current-clamp recordings were performed 1 week after injection. Voltage was recorded before and after CNO bath application. The scale bar represents 500 μm. The "+CNO" bar represents laser stimulation. The dots on the graph represent individual measurements. [Figure 9B] See legend to Figure 9A. [Figure 9C] See legend to Figure 9A. [Figure 10] Figures 10A and 10B show staining images and data plots associated with a study in which human brain tissue obtained from surgical resections was exposed to AAV-E2-dTomato and maintained in culture for 7–14 days. Figure 10A: Representative image of dendrites of virally labeled cells filled with biocytin during the recording procedure. Figure 10B: Slice recording of intrinsic properties of virally labeled neurons. Quantification is shown for the indicated parameters. The darker rightmost points in the "Identity" graph represent cells with typical fast-spiking (FS) properties. Scale bar represents 100 μm. Points on the graph represent individual measurements, and lines represent the mean + / - sem. [Figure 11-1] Figure 11 shows a table showing quantification of marker / reporter-expressing cells. Quantification was performed using a minimum of two independent biological replicates as described in Example 7. The table shows the specific number of cells and conditions for each individual quantification. [Figure 11-2] See description of Figure 11-1. [Figure 11-3] See description of Figure 11-1. [Figure 11-4] See description of Figure 11-1. [Figure 11-5] See description of Figure 11-1. [Figure 11-6] See description of Figure 11-1. [Figure 11-7] See description of Figure 11-1. [Figure 11-8] See description of Figure 11-1. [Figure 11-9] See description of Figure 11-1. [Figure 11-10] See description of Figure 11-1. [Figure 12] Shown is a UMAP plot of 3500 neuronal nuclei collected from four Dlx6aCre::Sun1-GFP mice reflecting promoter accessibility of the indicated classical interneuron markers. [Figure 13A-1] Figures 13A and 13B show slices, images, and graphs related to the identification of region-specific viral enhancers. Figure 13A: Adult mice were systemically injected with the indicated rAAV vectors containing an enhancer element polynucleotide sequence and a detectable reporter or marker (e.g., GFP) polynucleotide, i.e., rAAV-E[x]-eGFP, and analyzed 3 weeks after injection. Immunohistochemistry (IHC) for the reporter and the indicated markers in the S1 cortex was used to assess the density of neuronal cell bodies expressing the viral reporter (left panel) and the specificity of viral reporter expression for the indicated markers (right panel). For the E29 virus, no cell bodies were observed in the thalamus, except in the thalamic reticular nucleus (TRN). Figure 13B: Adult macaques were injected with rAAV-E22-eGFP into V1 and analyzed 8 weeks after injection using IHC for the reporter and the indicated markers. Scale bars represent 100 μm (a), 50 μm (b, left), and 10 μm (b, right). Points on the graphs represent individual measurements, and lines represent the mean + / - sem. [Figure 13A-2] See legend to Figure 13A-1. [Figure 13B] See legend to Figure 13A-1. [Figure 14] Figure 1 shows images and graphs related to a study in which adult mice were injected with the indicated modified rAAV-E2-dTomato constructs and analyzed 3 weeks after injection using a viral reporter and IHC for PV. The corresponding specificity is indicated to the right of the graph. The scale bar represents 2 μm. Points on the graph represent individual measurements, and the line represents the mean + / - sem. [Figure 15A-1] Figures 15A-1 and 15A-2 show a table containing specifications of all enhancers tested, including the associated gene, target population, specificity for the target population, location, presence of ATAC peaks, and conservation with the human sequence. [Figure 15A-2] See legend to Figure 15A-1. [Figure 16A-1]Figures 16A-1 and 16A-2 show tables compiling various parameters associated with each of the enhancers tested, including enhancer name (E1-E35), gene, target, % specificity, mouse chromosome location (mouse_mm10_Chr), enhancer sequence start site in the mouse genome (mouse_mm10_start), enhancer sequence stop site in the mouse genome (mouse_mm10_stop), size in base pairs (bp), human chromosome location (human_hg38_Chr), enhancer sequence start site in the human genome (human_hg38_start), enhancer sequence stop site in the human genome (human_hg38_stop), and percent conservation between the mouse and human enhancer sequences. In the tables shown in Figures 15A-1 and 15A-2, 16-A1 and 16-A2, and 1A1-1A3, the total number of base pairs (bp) shown for each polynucleotide sequence of listed enhancers E1-E35 reflects, as will be understood by one of skill in the art, that the first base pair (bp) counted in the sequence is zero (0). Nevertheless, the total number of bp comprising the polynucleotide sequence of each enhancer (E1-E35) can be obtained by simply counting the total number of bp in the sequence based on the tabulated data shown in the figures described herein. [Figure 16A-2] See legend to Figure 16A-1. DETAILED DESCRIPTION OF THE INVENTION

[0116] Detailed Description of the Present Embodiment Embodiments characterized and described herein relate to strategies, methods, and products developed to identify multiple novel enhancers (E1-E35) for use with viral vectors, e.g., recombinant adeno-associated viral (rAAV) vectors, for example, to target functionally distinct neuronal subtypes, particularly those located within the cerebral cortex. By examining the regulatory properties of the disease gene SCN1A, enhancers were identified that target the breadth of expression of the disease gene SCN1A, including, by way of non-limiting example, two enhancers selective for parvalbumin (PV) and vasoactive intestinal polypeptide (VIP) cortical interneurons. The functional utility of these regulatory elements was demonstrated, and the PV-specific enhancers were found to enable selective targeting and manipulation of these neurons across species, from mice to humans. Furthermore, the selection method described herein can be generalized to other genes and to certain characterized PV-specific enhancers with high specificity for distinct brain regions, such as E11, E14, E22, and E29. Recombinant viral vectors, such as rAAV vectors, carrying this enhancer sequence provide viral tools for use in cell-type-specific circuit manipulation and therapeutic intervention to treat and ameliorate neuropathological or neuropsychiatric diseases, conditions, and pathologies.

[0117] Specific viral-based therapeutic products, compositions, methods and approaches for treating or ameliorating neurological, neurodevelopmental, neurogenerative or neuropsychiatric diseases, disorders and pathologies are described herein.As described, viral vectors and vehicles for gene delivery are designed and produced to contain specific enhancer sequences (enhancers) and the polynucleotide sequences of genes of interest, such as effector genes (e.g., transgenes or reporter genes), which are specifically and functionally expressed in specific interneurons or neuronal cell populations after transduction of interneurons or neuronal cells by the viral vectors or vehicles.In one aspect, a viral vector or vehicle is provided that contains the polynucleotide of a specific enhancer sequence (enhancer), and is specifically and functionally expressed in specific interneurons or neuronal cell populations after transduction of interneurons or neuronal cells by the viral vectors or vehicles. In one embodiment, the enhancer carried by the virus can restrict transgene expression to certain interneuron or neuron cells. In an embodiment, transgene expression is restricted to cells defective in that gene. In one embodiment, transgene expression is specifically regulated in interneurons or other neuron cells. In another embodiment, the transgene is an effector gene or a therapeutic gene. In an embodiment, the enhancer element restricts gene expression to one or more neuron cell types, including fast-spiking cortical interneuron parvalbumin (PV)-expressing cortical interneuron cells (PV-cIN cells); vasoactive intestinal peptide (VIP)-expressing disinhibited cortical interneuron cells (VIP cIN cells); and pyramidal (PYR) neurons, particularly pyramidal neurons in cortical layer 5 of the brain.

[0118] In one embodiment, the viral vector contains a specific enhancer sequence and a transgene (effector gene) associated with a neurological, neurodevelopmental, or neurodevelopmental disease, disorder, or condition, where the enhancer can restrict expression of the transgene to interneuron cell populations that have a loss of function, are defective, or express a mutant, variant, or defective form of the gene associated with the neurological or neurodevelopmental disease, disorder, or condition. In a specific embodiment, the enhancer sequence inserted into the viral vector polynucleotide is identified as having the specificity to regulate expression of the SCN1A gene, which encodes the Nav1.1 sodium channel, and to restrict expression to SCN1A-expressing cells, particularly GABAergic interneuron cells. Loss of function of the SCN1A gene is the most common cause of Dravet syndrome (DS), a debilitating form of infantile epilepsy that is associated with cognitive impairment and premature death. In certain embodiments, the specific expression of transgene (effector gene) in interneurons can be confirmed by detecting markers specific to interneuron cells, such as, but not limited to, GABA GAD67 or PV interneuron cell markers. In one embodiment, the viral vector or vehicle is an adeno-associated virus (AAV) or recombinant AAV (rAAV). The terms "AAV" and "rAAV" are used interchangeably herein.

[0119] The term "transgene" is used herein to refer to a gene of interest (effector gene) contained in the rAAV vector or vehicle described herein, which is specifically expressed and functions in a specific cell type or population, as described herein, particularly due to an enhancer sequence also contained in the rAAV vector that restricts expression of the gene to a defined cell population, such as PV-expressing interneurons or SCN1A-expressing interneurons or subtypes thereof. In some cases, the gene of interest (effector gene) is expressed in the cell type transduced by rAAV, and the encoded product is a normal gene that functions to provide a normal or normally functioning product in cells, such as cells with a loss of function of the same gene as the transgene. In some cases, the transgene or effector gene may be a reporter gene, such as green fluorescent protein (GFP) or red fluorescent protein (RFP), that provides a detectable signal after transduction of cells with the rAAV vector. In some cases, the transgene or effector gene may be both a reporter and a gene encoding a product that, when expressed and active, results in normal cellular function. The latter type of gene may be considered a therapeutic gene. In certain embodiments, the rAAV contains an SCN1A-specific enhancer sequence and an SCN1A transgene.

[0120] The rAAV vectors and methods described herein are based, at least in part, on the discovery and demonstration that specific enhancers can restrict expression of a transgene carried by the viral vector, e.g., a gene or reporter gene associated with a neurological disease, disorder, or condition, to interneuron cells ("interneurons") located in the brain where the gene is expressed and where the encoded gene (transgene) product is functional. In one aspect, such an expressed functional gene offsets, replaces, or supersedes the abnormal, unusual, or lack of function of a gene encoding a product involved in the normal function of the interneuron cell.

[0121] In one embodiment, to restrict transgene expression to GABAergic PV-expressing interneurons in a mammal, a suitable viral vector, e.g., a lentiviral vector, or, in particular, a recombinant adeno-associated viral (rAAV) vector, is used, in which an enhancer element described herein is provided in cis. In an embodiment, the enhancer element is one of S5E1 (E1), S5E2 (E2), S5E3 (E3), S5E4 (E4), S5E6 (E6), S5E7 (E7), S5E8 (E8), S5E9 (E9), and S5E10 (E10). In embodiments, the enhancer element is E2, which can limit expression of the viral reporter to parvalbumin (PV)-expressing cortical interneurons (PV cINs), as described herein; E6, which is selective for VIP interneurons; or E5, which labels interneuron populations across all cortical layers but is particularly selective for pyramidal neurons in layer 5 of the cerebral cortex, particularly glutamatergic pyramidal neurons. In certain embodiments, the enhancer element is E2. In another particular embodiment, the enhancer element is E5. In yet another particular embodiment, the enhancer element is E6.

[0122] In one embodiment, the enhancer-containing viral vector or rAAV vector expresses one copy of SCN1A in transduced PV-expressing interneuron cells for the treatment and therapy of seizures, all forms of epilepsy, or DS. In other embodiments, the enhancer-containing vector or rAAV vector expresses an effector such as Gq-DREADD or PSAM for chemogenetic modulation of PV interneuron activity to treat epilepsy, including all forms of seizures, focal epilepsy, and pharmacologically refractory epilepsy, and also to treat DS and its symptoms.

[0123] Generally, the viral or rAAV vector comprises a polynucleotide comprising an enhancer sequence selected from S5E1-S5E10 described herein and a transgene sequence, e.g., a polynucleotide sequence encoding an SCN1A gene, a polynucleotide sequence encoding a hM3Dq modified muscarinic receptor (Gq-DREADD) receptor, or a polynucleotide sequence encoding a PSAM. In one embodiment, the polynucleotide comprises an enhancer sequence selected from E2, E5, or E6 described herein. In certain embodiments, methods are provided for therapeutic and prophylactic treatment of seizures and epilepsy, more specifically Dravet syndrome, in an individual (e.g., a human patient) in need thereof.

[0124] In one aspect, a method is provided in which a viral vector, such as a recombinant adeno-associated virus (rAAV) vector, is administered to an individual or subject in need thereof, for example, a patient suffering from seizures, epilepsy, or DS, comprising an enhancer sequence described herein, for example, E2, E5, or E6, and a transgene polynucleotide sequence encoding, for example, an SCN1A-encoding polynucleotide sequence, an hM3Dq modified muscarinic receptor (Gq-DREADD)-encoding polynucleotide sequence, or a PSAM-encoding polynucleotide sequence, so that SCN1A, Gq-DREADD, or PSAM is expressed in the interneurons of the individual or subject, particularly PV-expressing interneurons. Thus, a method is provided in which interneurons in an individual or subject in need thereof that do not express SCN1A, Gq-DREADD, or PSAM, particularly PV-expressing interneurons, are converted into interneurons that express SCN1A, Gq-DREADD, or PSAM, respectively. Thus, expression of the gene and encoded protein is linked to the presence of enhancer elements (E1-E10) described herein, which are also provided as components of the rAAV vector genome. In one embodiment, the enhancer element is E2, E5, or E6. In one embodiment, an individual or subject in need, e.g., a patient suffering from seizures, epilepsy, or DS, is administered a viral vector, such as a recombinant adeno-associated viral (rAAV) vector, comprising an enhancer sequence described herein, e.g., E2, and a transgene polynucleotide sequence encoding SCN1A.

[0125] In one embodiment, a prophylactic or therapeutic treatment method for the prevention and / or therapy of seizures, epilepsy, or DS is provided, comprising introducing into an individual or subject in need thereof a viral vector or rAAV vector comprising an enhancer sequence (E1-E10) described herein and a sequence encoding an SCN1A-encoding polynucleotide sequence, such that the severity of the seizures, epilepsy, or DS symptoms experienced by the individual or subject is reduced, or the seizures, epilepsy, or DS symptoms are treated or prevented. In one embodiment, the enhancer element is E2, E5, or E6. In one embodiment, the individual or subject in need thereof is experiencing seizures (e.g., epileptic seizures) or DS symptoms at the time of administration of the vector. After administration of the vector to the individual or subject, the severity of the seizures, epilepsy, or DS symptoms is reduced, or the seizures, epilepsy, or DS symptoms are treated or prevented.

[0126] In one embodiment, a method of prophylactic or therapeutic treatment for the prevention and / or therapy of seizures, epilepsy, or DS is provided, comprising introducing into an individual a viral vector or rAAV vector comprising an enhancer sequence (E1-E10) described herein and a sequence encoding an hM3Dq modified muscarinic receptor (Gq-DREADD)-encoding polynucleotide sequence, followed by administering to the individual an effective amount of a Gq-DREADD agonist to reduce the severity of the seizures, epilepsy, or DS symptoms, or to treat or prevent the seizures, epilepsy, or DS symptoms. In one embodiment, the enhancer element is E2, E5, or E6. In one embodiment, the individual or subject in need is experiencing a seizure (e.g., an epileptic seizure) upon administration of the Gq-DREADD receptor agonist. After administration of the agonist, the severity of the seizure is reduced. In embodiments, the Gq-DREADD receptor agonist is clozapine-N4-oxide (CNO) or another suitable Gq-DREADD receptor agonist known and used in the art.

[0127] In aspects of the treatment and prevention methods described herein, the individual or subject is experiencing partial or generalized seizures or is at risk of developing partial or generalized seizures. In other embodiments, the individual or subject has, is suspected of having, or has been diagnosed with any form of epilepsy, including but not limited to, drug-resistant epilepsy. According to the described methods, seizures, epilepsy, or DS symptoms are inhibited, blocked, reduced, alleviated, or prevented.

[0128] In one embodiment, a composition comprising a viral vector or rAAV vector is administered to a subject in need thereof. In one embodiment, administration of a composition comprising a vector comprising an enhancer element described herein, e.g., E1-E10, and a polynucleotide encoding SCN1A (or the vector itself) facilitates the conversion of interneurons or PV-expressing interneurons in the brain of an individual or subject that do not express SCN1A to interneurons or PV-expressing interneurons that express SCN1A. In another embodiment, administration of a composition comprising a vector comprising an enhancer element described herein, e.g., E1-E10, and a polynucleotide encoding a Gq-DREADD receptor (or the vector itself) facilitates the conversion of interneurons or PV-expressing interneurons in the brain of an individual or subject that do not express Gq-DREADD receptors to interneurons or PV-expressing interneurons that express Gq-DREADD receptors, thereby generating interneurons or PV-expressing interneurons that are responsive to Gq-DREADD agonists. In another embodiment, administration of a composition comprising an enhancer element described herein, e.g., E1-E10, and a vector comprising a polynucleotide encoding PSAM (or the vector itself) facilitates the conversion of an individual's or subject's interneurons that do not express PSAM or PV-expressing interneurons in the brain to interneurons that do express PSAM or PV-expressing interneurons. In one embodiment, the vectors, compositions, and methods described herein are used in the prophylactic or therapeutic treatment of partial and / or generalized seizures. In one embodiment, the enhancer element is E2, E5, or E6.

[0129] In one aspect, the vectors, compositions, and methods described herein may be used in the prophylactic or therapeutic treatment of various types of epilepsy, including but not limited to drug-resistant epilepsy, and / or may constitute an alternative to pharmacological treatment. In embodiments, the vectors, compositions, and methods described herein are used in the prophylactic or therapeutic treatment of one or more seizure disorders, including, but not limited to, epilepsy, including localization-related epilepsy, generalized epilepsy, epilepsy with generalized and / or focal seizures, seizures associated with Lennox-Gastaut syndrome, seizures as a complication of a disease or condition (e.g., encephalopathy, phenylketonuria, juvenile Gaucher disease, Unvericht-Lundborg's progressive myoclonic epilepsy, stroke, head trauma, stress, hormonal changes, drug use or withdrawal, alcohol use or abstinence, sleep deprivation, fever, infection, brain cancer, etc., or chemically induced seizure disorders).

[0130] In one embodiment, the vectors or rAAV vectors, compositions, and methods described herein are used in the prophylactic or therapeutic treatment of individuals or subjects in need thereof, such as individuals or subjects who have experienced and / or are at risk of experiencing seizures, and who may therefore be diagnosed with or suspected of having any seizure disorder. In one embodiment, administration of a viral vector or rAAV vector comprising an enhancer element and a transgene described herein may occur before the onset of a seizure, e.g., an epileptic seizure, or DS symptoms, for example, days, weeks, months, or years prior to administration. For example, those skilled in the art have demonstrated that rAAV-driven expression can persist for at least six years in a non-human primate model (Rivera, VM et al., 2005, Blood, 105:1424-1430).

[0131] In one embodiment, the rAAV vector containing the SCN1A-specific enhancer sequence also contains a capsid protein, which enhances the targeting ability of the viral vector and enables the vector to specifically transduce interneuron cells, such as GABAergic interneuron cells and / or a specific subpopulation of GABAergic interneuron cells, particularly those in the cerebral cortex of the brain. rAAV vectors that transduce GABAergic interneurons and rAAV vectors containing capsid proteins that increase the likelihood of the virus specifically transducing GABAergic interneurons, particularly the subpopulation of GABAergic interneurons that also express parvalbumin (PV), called PV-expressing interneurons (also called PV-expressing cortical interneurons), are highly suitable for use in the compositions and methods described herein. In another embodiment, rAAV vectors containing an SCN1A-specific enhancer sequence, e.g., E5, also contain a capsid protein that enhances the targeting ability of the viral vector and enables the vector to specifically transduce pyramidal neurons, e.g., glutamatergic pyramidal neuron cells of the brain cortex.

[0132] In one embodiment, the transgene (effector gene) inserted into the viral vector has a function (or loss of function) that has been found to be causally associated with neurological disorders characterized by seizures or adverse epilepsy symptoms, such as infantile febrile epilepsy or Dravet syndrome (DS). The enhancer sequence in the vector restricts expression of the transgene to interneurons or subtypes thereof, or neurons, e.g., pyramidal neurons, and specifically regulates, e.g., increases or enhances, the expression of a normal, functional version of the gene in interneuron cells. In one embodiment, the interneuron is a GABAergic interneuron cell. In one embodiment, the interneuron GABAergic cell is a PV-expressing interneuron cell. In one embodiment, the neuron cell is a pyramidal neuron cell. In one embodiment, the pyramidal neuron cell is a glutamatergic pyramidal neuron.

[0133] In certain embodiments, the AAV vectors, vector-based compositions, and delivery and treatment methods provided herein are useful for treating patients suffering from Dravet syndrome (DS) and its significant symptoms, such as epilepsy and associated seizures. In one embodiment, the patient is a human patient, particularly an infant or young child suffering from DS. As further described below, Dravet syndrome (DS) is a type of infantile epilepsy associated with many significant symptoms, including cognitive impairment and life-threatening seizures. Loss of function of the sodium channel Nav1.1, encoded by the SCN1A gene, is the most common cause of DS. Previous studies using DS mouse models suggest that the cause is loss of SCN1A gene function in GABAergic interneurons, the primary defect underlying seizures, the most damaging symptom of this syndrome. Currently, there is no reliable treatment that eliminates or reduces seizures in DS patients. Therefore, the viral products, compositions, and methods described herein provide a much-needed and highly beneficial treatment for patients suffering from DS.

[0134] Thus, in certain embodiments, the transgene or effector gene contained in the AAV vector or vehicle is SCN1A, and the enhancer is a nucleic acid sequence (e.g., a cis-acting regulatory element in the AAV vector) that restricts expression of the SCN1A gene to SCN1A-expressing interneurons and is specific for regulating expression of the SCN1A gene in interneuron cells, e.g., GABAergic interneurons or PV-expressing GABAergic interneurons. In another specific embodiment, the transgene or effector gene contained in the AAV vector or vehicle is SCN1A, and the enhancer is a nucleic acid sequence (e.g., a cis-acting regulatory element in the AAV vector) that restricts expression of the SCN1A gene to SCN1A-expressing pyramidal neurons and is specific for regulating expression of the SCN1A gene in pyramidal neuron cells, e.g., glutamatergic pyramidal neurons, in the brain cortex, e.g., in cortical layer 5 of the brain.

[0135] A method utilizing molecularly engineered AAV vectors designed with a specific enhancer that restricts expression of the normal SCN1A effector gene encoding the Nav1.1 sodium channel to interneuron cells specifically involves transducing interneuron cells in a subject with a vector containing an SCN1A-specific enhancer sequence and the SCN1A gene, resulting in expression of the gene in interneurons, and administering a therapeutically effective amount of a viral vector, viral particle, or pharmaceutical composition containing the viral vector or particle to a subject (e.g., a human infant with DS) to produce a functional response in the subject's interneuron cells after administration, e.g., providing a functional Nav1.1 sodium channel or increasing sodium channel function. Functional expression of SCN1A in the transduced interneuron cells normalizes the excitability of interneuron cell populations deficient in SCN1A, such as GABAergic interneurons and PV-expressing GABAergic interneurons. This result restores the delicate E / I balance in brain regions.

[0136] To successfully and specifically express genes contained in AAVs as a form of therapy for DS, we developed an approach to explore the regulatory properties of this effector gene to identify enhancer polynucleotide sequences that can specifically restrict expression to neuronal cell populations defective in the SCN1A gene (Figures 3A-3D). In one embodiment, the enhancer sequence is a cis-acting element that regulates, e.g., increases, enhances, augments, or otherwise improves, expression of the SCN1A gene, particularly in interneuron cells, e.g., GABAergic interneuron cells or PV-expressing GABAergic interneuron cells, and particularly in interneurons with loss of function of the SCN1A gene. In one embodiment, the enhancer sequence is a cis-acting element that regulates, e.g., increases, enhances, augments, or otherwise improves, expression of the SCN1A gene, particularly in pyramidal neurons, e.g., glutamatergic pyramidal neuron cells. The terms "enhancer" and "enhancer element" are used interchangeably herein. The term "enhancer element" is sometimes referred to herein as "regulatory element."

[0137] In one embodiment, the enhancer polynucleotide sequence that specifically regulates expression of the SCN1A gene in interneuron cells has a length of about 25-50, 50-100, 100-150, 150-200, 200-250, 250-300, 300-350, 350-400, 400-450, 450-500, 500-550, 550-600, 600-650, 650-700, 700-750, 750-800, 800-850, 850-900, 900-95 The PV-specific enhancer sequences may be 0, 950-1000, 1050, 1100, 1150, 1200, 1250, 1300, 1350, 1400, 1450, 1500, 1550, 1600, 1650, 1700, 1650, 1800, 1850, 1900, 1950, 2000, 2050, or 2500 nucleotides (base pairs (bp)), or longer, e.g., longer than 2500 nucleotides (bp), including all greater and lesser values within these above bp lengths. In some embodiments, PV-specific enhancer sequences suitable for use are 261 bp, 521 bp, 547 bp, 606 bp, 618 bp, 663 bp, 832 bp, 1280 bp, 1644 bp, or 2430 bp. In other embodiments, PV-specific enhancer sequences suitable for use are 267 bp, 586 bp, 636 bp, 665 bp, 844 bp, 849 bp, 894 bp, 1636 bp, 1766 bp, or 5124 bp. Enhancer sequences with specificity for regulating (e.g., enhancing) expression of the SCN1A gene in interneuron cells may be derived from genomic polynucleotides, e.g., intronic or intergenic sequences of DNA or RNA (Figures 1A-1 to 1A-3).

[0138] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more that have at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following mouse polynucleotide (DNA) sequence (E1), also referred to as "S5E1," located at start / stop positions 66256056 / 66257335 on chromosome 2 shown in FIG. 1A-1 , or a human ortholog thereof: TIFF2025118768000007.tif76146

[0139] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more that have at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following mouse polynucleotide (DNA) sequence (E2), also referred to as "S5E2," located at start / stop positions 66364036 / 66364653 on chromosome 2 shown in FIG. 1A-1 , or a human ortholog thereof: TIFF2025118768000008.tif58146

[0140] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more that have at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following mouse polynucleotide (DNA) sequence (E3), also referred to as "S5E3," located at start / stop positions 66383190 / 66384021 on chromosome 2 shown in FIG. 1A-1 , or a human ortholog thereof: TIFF2025118768000009.tif76146

[0141] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more that have at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following mouse polynucleotide (DNA) sequence (E4), also referred to as "S5E4," located at start / stop positions 66387764 / 66388024 on chromosome 2 shown in FIG. 1A-1 , or a human ortholog thereof: TIFF2025118768000010.tif29146

[0142] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more that have at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following mouse polynucleotide (DNA) sequence (E5), also referred to as "S5E5," located at start / stop positions 66392447 / 66393109 on chromosome 2 shown in FIG. 1A-1 , or a human ortholog thereof: TIFF2025118768000011.tif58146

[0143] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more that have at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following mouse polynucleotide (DNA) sequence (E6), also referred to as "S5E6," located at start / stop positions 66401767 / 66402372 on chromosome 2 shown in FIG. 1A-1 , or a human ortholog thereof: TIFF2025118768000012.tif60146

[0144] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more that have at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following mouse polynucleotide (DNA) sequence (E7), also referred to as "S5E7," located at start / stop positions 66407834 / 66410263 on chromosome 2 shown in FIG. 1A-1 , or a human ortholog thereof: TIFF2025118768000013.tif144146

[0145] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more that have at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following mouse polynucleotide (DNA) sequence (E8), also referred to as "S5E8," located at start / stop positions 66439814 / 66441457 on chromosome 2 shown in FIG. 1A-1 , or a human ortholog thereof: TIFF2025118768000014.tif101146

[0146] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more that have at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following mouse polynucleotide (DNA) sequence (E9), also referred to as "S5E9," located at start / stop positions 66441748 / 66442268 on chromosome 2 shown in FIG. 1A-1 , or a human ortholog thereof: TIFF2025118768000015.tif46146

[0147] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more that have at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following mouse polynucleotide (DNA) sequence (E10), also referred to as "S5E10," located at start / stop positions 66450594 / 66451140 on chromosome 2 shown in FIG. 1A-1 , or a human ortholog thereof: TIFF2025118768000016.tif52146

[0148] In one aspect, the human sequences (human orthologous sequences) of the 10 mouse enhancer sequences were determined based on the alignment of the mouse and human genome sequences of SCN1A, including 100 kb upstream and 100 kb downstream sequences. Thus, human orthologous sequences that are highly conserved between the mouse and human sequences were identified.

[0149] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence designated herein as E1 or S5E1, located at human_hg38 start165953030 / human_hg38 stop165954796 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000017.tif104146

[0150] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, referred to herein as E2 or S5E2, located at human_hg38 start166084035 / human_hg38 stop166084884 (Figures 1A-2 and 1A-3) of the human genome sequence: TIFF2025118768000018.tif77146

[0151] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, referred to herein as E3 or S5E3, located at human_hg38 start166090876 / human_hg38 stop166091720 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000019.tif77146

[0152] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50 to 500 bp or more, 50 to 250 bp or more, 100 to 200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, referred to herein as E4 or S5E4, located at human_hg38 start166094366 / human_hg38 stop166094633 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000020.tif28146

[0153] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, referred to herein as E5 or S5E5, located at human_hg38 start166103693 / human_hg38 stop166104587 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000021.tif82146

[0154] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, referred to herein as E6 or S5E6, located at human_hg38 start166118214 / human_hg38 stop166118879 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000022.tif65146

[0155] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50 to 500 bp or more, 50 to 250 bp or more, 100 to 200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, referred to herein as E7 or S5E7, located at human_hg38 start165892760 / human_hg38 stop165897884 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000023.tif119146TIFF2025118768000024.tif180146

[0156] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, referred to herein as E8 or S5E8, located at human_hg38 start166148156 / human_hg38 stop166149792 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000025.tif142146

[0157] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50 to 500 bp or more, 50 to 250 bp or more, 100 to 200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, referred to herein as E9 or S5E9, located at human_hg38 start166150066 / human_hg38 stop166150702 (Figures 1A-2 and 1A-3) of the human genome sequence: TIFF2025118768000026.tif59146

[0158] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, referred to herein as E10 or S5E10, located at human_hg38 start166160023 / human_hg38 stop166160609 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000027.tif53146

[0159] In one embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of about 100 bp or more that have at least 75% or more sequence identity to the human polynucleotide (DNA) sequence of the E1 (S5E1) to E10 (S5E10) enhancer element sequences described above (e.g., SEQ ID NOs:15-24). In another embodiment, the SCN1A-specific enhancer sequence comprises a nucleotide sequence containing one or more regions of about 100 bp or more that have at least 75% or more sequence identity to the human polynucleotide (DNA) sequence of the E2 (S5E2) enhancer element sequence described above (e.g., SEQ ID NO:16).

[0160] In another aspect, the enhancer sequences described herein include a nucleotide sequence containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated herein as E11, located at human_hg38 start 36816984 / human_hg38 stop 36817612 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000028.tif58146

[0161] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E12 herein, located at human_hg38 start 36817484 / human_hg38 stop 36817720 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000029.tif23146

[0162] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E13 herein, located at human_hg38 start 36818134 / human_hg38 stop 36818727 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000030.tif53146

[0163] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence designated herein as E14, located at human_hg38 start 88802240 / human_hg38 stop 88802877 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000031.tif58146

[0164] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E15 herein, located at human_hg38 start 88803290 / human_hg38 stop 88803678 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000032.tif34146

[0165] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E16 herein, located at human_hg38 start 88807290 / human_hg38 stop 88807962 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000033.tif64146

[0166] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E17 herein, located at human_hg38 start 88833390 / human_hg38 stop 88833984 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000034.tif52146

[0167] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E18 herein, located at human_hg38 start128377753 / human_hg38 stop128378783 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000035.tif94146

[0168] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E19 herein, located at human_hg38 start128289803 / human_hg38 stop128290279 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000036.tif46146

[0169] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E20 herein, located at human_hg38 start128323153 / human_hg38 stop128323718 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000037.tif52146

[0170] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E21 herein, located at human_hg38 start 128332503 / human_hg38 stop 128332974 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000038.tif47146

[0171] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E22 herein, located at human_hg38 start128336003 / human_hg38 stop128336491 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000039.tif47146

[0172] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E23 herein, located at human_hg38 start128365603 / human_hg38 stop1283366181 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000040.tif52146

[0173] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E24 herein, located at human_hg38 start 128375853 / human_hg38 stop 128376606 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000041.tif70146

[0174] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E25 herein, located at human_hg38 start128408553 / human_hg38 stop128408930 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000042.tif34146

[0175] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E26 herein, located at human_hg38 start 13388723 / human_hg38 stop 13390212 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000043.tif131146

[0176] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E27 herein, located at human_hg38 start 13469123 / human_hg38 stop 13470861 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000044.tif154146

[0177] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E28 herein, located at human_hg38 start 31124894 / human_hg38 stop 31125629 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000045.tif64146

[0178] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E29 herein, located at human_hg38 start 31132544 / human_hg38 stop 31133831 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000046.tif113146

[0179] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E30 herein, located at human_hg38 start 88655733 / human_hg38 stop 88657379 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000047.tif148146

[0180] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E31 herein, located at human_hg38 start 88872683 / human_hg38 stop 88872997 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000048.tif29146

[0181] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E32 herein, located at human_hg38 start 88745133 / human_hg38 stop 88745535 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000049.tif40146

[0182] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E33 herein, located at human_hg38 start 88799783 / human_hg38 stop 88801354 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000050.tif142146

[0183] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E34 herein, located at human_hg38 start 27969472 / human_hg38 stop 27969690 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000051.tif22146

[0184] In another aspect, the enhancer sequences described herein include nucleotide sequences containing one or more regions of 50-500 bp or more, 50-250 bp or more, 100-200 bp or more, or 100 bp or more having at least 70% or more, at least 75% or more, at least 80% or more, at least 85% or more, at least 90% or more, or at least 95% or more sequence identity to the following human polynucleotide (DNA) sequence, designated E35 herein, located at human_hg38 start 27973822 / human_hg38 stop 27974489 of the human genome sequence (Figures 1A-2 and 1A-3): TIFF2025118768000052.tif58146

[0185] In one embodiment, the enhancer sequences described herein comprise a nucleotide sequence containing one or more regions of about 100 bp or greater that have at least 75% or greater sequence identity to the human polynucleotide (DNA) sequence of the E11-E35 enhancer element sequences described above (e.g., SEQ ID NOs:25-49). In another embodiment, the enhancer sequence comprises a nucleotide sequence containing one or more regions of about 100 bp or greater that have at least 75% or greater sequence identity to the human polynucleotide (DNA) sequence of, for example, the E1 (SEQ ID NO:15), E2 (SEQ ID NO:16), E5 (SEQ ID NO:19), E6 (SEQ ID NO:20), E11 (SEQ ID NO:25), E14 (SEQ ID NO:28), E22 (SEQ ID NO:36), or E29 (SEQ ID NO:43) enhancer element sequences described above.

[0186] Genetic Epilepsy with Febrile Seizures plus (GEFS+) and Dravet Syndrome Genetic epilepsy with febrile seizures plus (GEFS+) is a rare condition that constitutes a spectrum of seizure disorders with varying degrees of severity. GEFS+ is usually diagnosed in families in which members have a combination of fever-induced febrile seizures and other types of recurrent seizures (epilepsy), including seizures not associated with fever (afebrile seizures). An additional type of seizure, called generalized seizures, typically involves both sides of the brain. However, some affected individuals experience seizures that involve only one side of the brain (partial seizures). The most common types of seizures in GEFS+ individuals include myoclonic seizures, which cause involuntary muscle spasms; atonic seizures, which involve sudden onset of weak muscle tone; and absence seizures, which cause brief periods of loss of consciousness that manifest as staring spells. GEFS+ is usually diagnosed in families, but it can also occur in individuals with no family history of the condition.

[0187] The most common and mildest feature of the GEFS+ spectrum is simple febrile seizures, which begin in infancy and typically resolve by age 5. When febrile seizures persist beyond age 5, or when other types of seizures develop, the condition is called febrile seizures plus (FS+) and typically resolves during early adolescence.

[0188] Dravet syndrome (DS), also known as severe myoclonic epilepsy in infancy (SMEI) or early infantile epileptic encephalopathy-6 (EIEE6), is a condition often considered part of the GEFS+ spectrum and is the most severe of this group of disorders. Because not all affected individuals exhibit myoclonic epilepsy, the term Dravet syndrome is preferred. Affected infants typically have prolonged seizures lasting several minutes (status epilepticus) and are precipitated by fever. Other types of seizures, including afebrile seizures, begin in early childhood. These seizure types may include myoclonic or absence seizures. In Dravet syndrome, these seizures are difficult to manage with medication and may worsen over time. Deterioration of brain function is also common in Dravet syndrome. Children with Dravet syndrome typically present with symptoms within the first year of life, but the condition stalls thereafter. Some affected children lose previously acquired abilities and experience developmental regression. Many children suffering from Dravet syndrome have difficulty coordinating their movements (ataxia) and are intellectually disabled.

[0189] Causes of GEFS+ Mutations in several genes, including unspecified mutations, can cause GEFS+. The most commonly associated gene is SCN1a. Alterations in this gene cause more than 80% of Dravet syndrome cases and approximately 10% of other GEFS+ cases. Mutations in other genes have been found in only a small number of affected individuals or families. The SCN1A gene and other genes associated with GEFS+ encode subunits of ion channels that transport positively charged ions into cells. The transport of these ions generates electrical signals and helps transmit them between neurons (nerve cells). Mutations in the SCN1A gene have various effects on sodium channels. Many genetic mutations that cause or are associated with Dravet syndrome reduce the number of functional channels in each cell. Mutations that cause milder GEFS+ disorders likely alter channel structure. All of these genetic changes affect the channel's ability to transport sodium ions into neurons. Some harmful mutations are thought to reduce channel activity, while others may increase it. "Changes in GABAergic receptor subunit genes impair channel function, leading to uncontrolled signaling between neurons, which likely leads to seizures. While I don't want to be bound by theory and don't intend to, some studies have reported that certain SCN1A gene mutations cause constant signaling stimulation between neurons. This overstimulation of certain neurons in the brain induces abnormal brain activity associated with seizures."

[0190] Although it is not known whether all SCN1A gene mutations have the same effect, genome-wide association studies have demonstrated that loss of function of the voltage-gated sodium channel Nav1.1, encoded by the SCN1A gene, is the most common cause of Dravet syndrome. Previous studies using mouse models of Dravet syndrome suggest that it is loss of SCN1A function in GABAergic interneurons, the primary defect underlying the seizures that are the most detrimental symptom of this syndrome.

[0191] In animal studies, SCN1A- / - mice were found to develop severe ataxia and seizures and die on postnatal day 15. SCN1A+ / - mice exhibited spontaneous seizures and sudden death beginning after postnatal day 21, with a notable dependence on genetic background. Loss of SCN1A did not alter the voltage-dependent activation or inactivation of sodium channels in hippocampal neurons. However, sodium current density was significantly reduced in inhibitory interneurons of SCN1A- / - and + / - mice (Yu, FH et al., 2006, Nat Neurosci, 9(9):1142-1149; Yu et al., 2007, Nat Neurosci, 10(1):134). These studies suggest that reduced sodium currents in GABAergic inhibitory interneurons caused by heterozygous SCN1A mutations may contribute to the hyperexcitability leading to epilepsy in SMEI patients.

[0192] GABAergic cortical interneurons GABAergic interneurons release the neurotransmitter gamma-aminobutyric acid (GABA) and are central inhibitory neurons essential for the regulation and maintenance of neural circuits and activity. (Kelsom, C. and Lu, W., 2013, Cell Biosci., 3:19) GABAergic interneurons in the mammalian cerebral cortex comprise several distinct cortical interneuron subtypes that can be broadly classified and categorized by expressed protein markers.

[0193] Interneurons play a crucial role in the wiring and neural circuits of the developing nervous system in both invertebrate and vertebrate organisms. Generally, interneurons are a specialized type of neuron (nerve cell) whose primary role is to form connections with other types of neurons. Interneurons are neither motor nor sensory neurons, and they differ from projection neurons in that they send signals to distant locations, such as the brain or spinal cord. Importantly, interneurons function to regulate neural circuits and circuit activity. The majority of interneurons in the central nervous system are inhibitory interneurons. In contrast to excitatory neurons, inhibitory cortical interneurons typically release the neurotransmitters gamma-aminobutyric acid (GABA) and glycine. Cortical interneurons are located in the cerebral cortex, which is defined as the outer layer of neural tissue that functions to cover the cerebral and cerebellar structures in the brain. (Ibid.)

[0194] GABAergic interneurons include numerous interneuron subtypes that can be broadly classified by the surface markers they express. The four major cortical interneuron subtypes are parvalbumin (PV)-expressing interneurons, somatostatin (SST)-expressing interneurons (which constitute a heterogeneous population), and ionotropic serotonin receptor 5HT3a (5HT3aR)-expressing interneurons. Together, these three subtypes account for approximately 100% of the neocortical GABAergic interneuron population in mice. These interneurons reside in each layer of the cerebral cortex, but originate in various subpallial locations and subsequently migrate into the cerebral cortex.

[0195] Cortical circuit function is maintained by a balance between excitatory and inhibitory inputs, and disruption of this balance likely contributes to the development of neurological, neurodevelopmental, or neuropsychiatric disorders, including but not limited to epilepsy, autism spectrum disorder, and intellectual disability.

[0196] The role of GABAergic cortical interneurons GABAergic neurons play an inhibitory role, releasing the neurotransmitter GABA into synapses to regulate the firing rate of target neurons. Neurotransmitter release typically occurs via postsynaptic GABA receptors to trigger neuronal signaling pathways. A They act through ionotropic receptors. The role / function of interneurons is typically divided into three components: (1) afferent input, (2) intrinsic properties of the interneuron, and (3) the interneuron's targets. Generally, interneurons receive input from various sources, including pyramidal cells and cells derived from other cortical and subcortical regions (Kelsom, C. and Lu, W., 2013, Cell Biosci., 3:19). Regarding output, cortical interneurons participate in feedforward and feedback inhibition. Regardless of the output type, the cortical interneuron network is further complicated by the fact that a single cortical interneuron can have multiple connections with excitatory neuronal targets.

[0197] Cortical interneuron subtypes It is estimated that there are over 20 different GABAergic interneuron subtypes in the cerebral cortex. Subtypes are also distinguished from one another based on the calcium-binding proteins they express, which serve as markers. Based on studies conducted in both mouse and rat brain tissue, the calcium-binding protein parvalbumin (PV) and the neuropeptide somatostatin (SST) have been identified as key markers for defining the most predominant interneuron subtypes within the cerebral cortex. Notably, the expression of these markers does not overlap, making the PV-expressing interneuron population independent of the SST-expressing population. In addition to PV- and SST-positive GABAergic interneurons, which together comprise approximately 70% of the total GABAergic cortical interneuron population, a separate interneuron subgroup expressing 5HT3aR has been found to comprise approximately 30% of all interneurons. These three interneuron subpopulations account for nearly 100% of all GABAergic cortical interneurons. However, each of these populations, particularly the 5HT3aR-expressing population, is heterogeneous and expresses other proteins or neuropeptides that contribute to their characterization (Kelsom, C. and Lu, W., 2013, Cell Biosci., 3:19).

[0198] Parvalbumin (PV)-expressing interneurons PV-expressing interneurons account for approximately 40% of the GABAergic cortical interneuron population. This interneuron population has a fast-spiking pattern and fires sustained high-frequency trains of brief action potentials. These interneurons also have the smallest input resistance and the fastest membrane time constant of all interneurons.

[0199] Two types of PV interneurons, basket cells and chandelier cells, constitute the PV interneuron group. Basket cells synapse on the soma and proximal dendrites of target neurons and are typically multipolar interneurons. Several studies have shown that fast-spiking basket neurons are the primary inhibitory system in the neocortex, mediating rapid inhibition of target neurons, among other functions. These fast-spiking basket neurons likely play a major role in regulating the delicate balance between excitatory and inhibitory inputs in the cerebral cortex. Unlike basket neurons, the chandelier cell subgroup of PV-expressing interneurons targets the axon initial segments of pyramidal neurons. Although both basket cells and chandelier cells are fast-spiking, they differ in their electrophysiological properties. In contrast to other interneurons, chandelier cells may be excitatory rather than inhibitory due to their depolarizing effect on the membrane potential. (Kelsom, C. and Lu, W., 2013, Cell Biosci., 3:19).

[0200] In the neocortex, e.g., mouse neurocortex, another group of PV-expressing cells, independent of chandelier and basket neurons, is called multipolar bursting cells. These cells differ from chandelier and basket cells in electrophysiology and connectivity. Multipolar bursting neurons synapse with pyramidal cells (or other multipolar bursting cells) that exhibit paired-pulse facilitation. In contrast, chandelier and basket cells are typically strongly inhibitory. (Kelsom, C. and Lu, W., 2013, Cell Biosci., 3:19)

[0201] Somatostatin (SST)-expressing interneurons SST-expressing interneurons constitute the second largest interneuron group in the mouse neocortex, accounting for approximately 30% of the total cortical interneuron population. SST GABAergic interneurons are a heterogeneous population of cortical interneurons. SST-positive interneurons, called Martinotti cells, have ascending axons that branch in layer I of the cerebral cortex and establish synapses on dendritic tufts of pyramidal neurons. Martinotti cells are also found in layers II–VI of the cortex, but are most abundant in layer V. In contrast to PV-positive interneurons, excitatory inputs to Martinotti cells are strongly facilitatory. Further subpopulations of SST-expressing cortical interneurons show differences in firing properties, expression of molecular markers, and connectivity of various neurons within this population. (Kelsom, C. and Lu, W., 2013, Cell Biosci., 3:19)

[0202] 5HT3aR-expressing interneurons A third population of GABAergic cortical interneurons, termed the 5HT3aR interneuron group, accounts for approximately 30% of the GABAergic cortical interneuron population. Based on mouse studies, this population of GABAergic interneurons in the cortex expresses 5HTa3 receptors but not PV or SST.

[0203] 5HT3aR interneurons are a heterogeneous population. Within the 5HT3aR interneuron group, there are several interneuron subsets that also express other protein or neuropeptide markers, including vasoactive intestinal polypeptide (VIP). VIP-expressing interneurons are localized in cortical layers II and III. While VIP-expressing interneurons do not express PV or SST, they do express the 5HTa3 receptor and account for approximately 40% of the 5HT3aR population. VIP interneurons generally synapse within dendrites, and some have been observed to target other interneurons. Compared to other cortical interneurons, VIP interneurons have a very high input resistance and are among the most excitable interneurons.

[0204] Sixty percent of cortical interneurons in the 5HT3aR-expressing population do not express VIP. Of this VIP-negative 5HT3aR group, nearly 80% express the interneuron marker reelin. Within this latter category of cortical interneurons, a population of neurogliaform cells, called spiderweb cells, express neuropeptide Y (NPY) and exhibit multiple dendrites radiating from a circular cell body. In contrast to other types of interneurons, which can only synapse on homologous neurons, neurogliaform interneurons can form synaptic connections with each other and with other interneuron types. Thus, neurogliaform cells use slow GABA receptors to elicit long-lasting inhibitory postsynaptic potentials on pyramidal neurons and other interneurons. A and GABA B They play an important role in regulating neural circuits and function by activating receptors.

[0205] pyramidal neurons Pyramidal neurons, also known as pyramidal cells, are neurons with a pyramidal-shaped cell body (soma) ranging from 20 to 120 μm in diameter and two distinct dendritic arbors. Basal dendrites arise from the base, and apical dendrites arise from the apical end of the pyramidal cell body. Like most neurons, pyramidal neurons have multiple dendrites and a single axon, but both the dendrites and axon are extensively branched. Pyramidal neuron dendrites are typically considered input structures, receiving synaptic connections from other neurons, while the axon serves as an output to other neurons. Pyramidal neuron dendrites can also release retrograde signaling molecules (e.g., endocannabinoids), so communication is somewhat bidirectional. Extensive branching of dendrites and axons allows a single neuron to communicate with thousands of other neurons in a network. (Spruston, N., 2009, Scholarpedia, 4(5):6130).

[0206] Pyramidal neurons are found in forebrain structures such as the cerebral cortex, hippocampus, and amygdala of mammals, birds, fish, and reptiles, but not in the olfactory bulb, striatum, midbrain, hindbrain, or spinal cord. Pyramidal neurons are the most abundant members of the excitatory neuron family in brain regions where they are present, such as cortical structures. These neurons release the neurotransmitter glutamate. Their abundance suggests their important role in nervous system function and cognitive processing. Pyramidal neurons comprise approximately two-thirds of all neurons in the mammalian cerebral cortex, where they function to convert synaptic inputs into patterned action potential outputs. Pyramidal neurons receive synaptic input from tens of thousands of excitatory synapses and thousands of inhibitory synapses. Most excitatory inputs, such as glutamatergic pyramidal neurons, use glutamate as a neurotransmitter, whereas inhibitory inputs use GABA.

[0207] Although the nature of the stimulus determines the type of output a pyramidal neuron produces (e.g., single spike vs. burst), intrinsic neuronal excitability is another important determinant of how the neuron responds to input. Neurons are typically classified according to how they respond to current injection, which can vary among pyramidal neuron types. Most pyramidal neurons respond to successive depolarizing current injections with a train of spikes, indicating spike-frequency adaptation (adaptation). Many pyramidal neurons respond with one or more bursts of action potentials. The nature of this response is determined primarily by the type of voltage-gated ion channels expressed in the neuron, but the structure of the dendritic tree is also important (Mainen, ZF et al., 1996, Nature, 382:363-366; Spruston, N., 2008, Nature Reviews Neuroscience, 9:206-221; Spruston, 2009, Scholarpedia, 4(5):6130).

[0208] Adeno-associated virus (AAV) AAV is a small (25 nm), non-enveloped virus containing a linear, single-stranded DNA genome packaged in a viral capsid. AAV belongs to the Parvoviridae family and the Dependovirus genus, as productive infection by AAV occurs only in the presence of adenovirus or herpesvirus helper viruses. In the absence of helper virus, AAV (serotype 2) can transduce cells and establish latency by specific, but rare, integration into chromosome 19q13.4. Thus, AAV is the only mammalian DNA virus known to be capable of site-specific integration. (Daya, S. and Berns, KI, 2008, Clin. Microbiol. Rev., 21(4):583-593)

[0209] After successful infection, the AAV life cycle progresses through two stages: the lytic stage and the lysogenic stage. The lytic stage persists in the presence of adenovirus or herpesvirus helper viruses. During this period, AAV undergoes productive infection, characterized by genome replication, viral gene expression, and virion production. Adenovirus genes that provide helper functions for AAV gene expression include E1a, E1b, E2a, E4, and VA RNA. While adenovirus and herpesvirus provide different sets of helper functions, both regulate cellular gene expression, creating a permissive intracellular environment for productive AAV infection. Herpesviruses support AAV gene expression by providing viral DNA polymerase and helicase, as well as early functions required for HSV transcription.

[0210] In the absence of adenovirus or herpesvirus, AAV replication is limited, viral gene expression is suppressed, and the AAV genome can establish latency by integrating into a 4-kb region on chromosome 19 (q13.4) called AAVS1. The AAVS1 locus is near several muscle-specific genes, TNNT1 and TNNI3. The AAVS1 region itself is upstream of MBS85, a gene whose product has been shown to be involved in actin organization. Tissue culture experiments suggest that the AAVS1 locus is a safe integration site.

[0211] Recombinant AAV (rAAV) as a vector for gene delivery and therapeutic treatment AAVs are well suited for use as vectors and vehicles for gene transfer into the nervous system, enabling gene expression and knockdown, gene editing, circuit modulation, in vivo imaging, disease model development, and evaluation of therapeutic candidates for treating neurological diseases. AAVs provide safe, long-term expression in the nervous system. Most of the aforementioned applications rely on local AAV injection into the adult brain to bypass the blood-brain barrier (BBB) and to temporally and spatially restrict transgene expression.

[0212] AAV vectors have been highly successful in meeting all of the desirable characteristics of a delivery vehicle, including the ability to attach to and enter target cells, successfully translocate to the nucleus, maintain nuclear expression for sustained periods, and an overall lack of pathogenicity and toxicity. Recombinant AAV (rAAV) is advantageous as a delivery vector, particularly for delivery to interneurons in brain tissue, because it is locally injectable, exhibits stable expression over long periods, is nonpathogenic, and does not integrate into the genome of transduced cells. Twelve human AAV serotypes (AAV serotype 1 (AAV-1) to AAV-12) and over 100 serotypes derived from nonhuman primates have been reported to date (Daya, S. and Berns, K. I., 2008, Clin. Microbiol. Rev., 21(4):583-593). Furthermore, rAAV has been approved by the FDA for use as a vector in at least 38 protocols for several different human clinical trials. AAV's lack of pathogenicity, persistence, and its many available serotypes have enhanced the virus's potential as a delivery vehicle for gene therapy applications according to the compositions and methods described.

[0213] Recombinant AAV (rAAV) vectors have been constructed that do not encode replication (Rep) proteins and lack the cis-active 38-base pair integration efficiency element (IEE) required for frequent site-specific integration. The inverted terminal repeats (ITRs) are cis signals required for packaging, so they are retained. Therefore, current recombinant AAV (rAAV) vectors persist primarily as extrachromosomal elements.

[0214] Recombinant AAV (rAAV) vectors for gene therapy have primarily been based on the AAV-2 serotype. AAV-2-based rAAV vectors can transduce muscle, liver, brain, retina, and lung, and require several weeks for optimal expression. The efficiency of rAAV transduction depends on the efficiency of each AAV infection step: viral binding, entry, transport, nuclear entry, uncoating, and second-strand synthesis.

[0215] Several novel AAV vector technologies have been developed to increase the genome capacity of AAV or enhance gene expression. Trans-splicing AAV vectors have been used to increase the vector's capacity to accommodate heterologous polynucleotides by exploiting AAV's ability to form head-to-tail concatemers through recombination in the ITRs. In this approach, a transgene cassette is split between two rAAV vectors containing appropriately positioned splice donor and acceptor sites. Transcription from the recombined AAV molecules, followed by correct splicing of the mRNA transcript, generates a functional gene product. While slightly less efficient than rAAV vectors, trans-splicing AAV vectors enable delivery of therapeutic genes up to 9 kb in size and have been successfully used for gene expression in the retina, lung, and muscle.

[0216] The rAAV-encoding polynucleotides described herein contain an SCN1A enhancer polynucleotide sequence. Due to their nature as enhancers, the orientation of the enhancer polynucleotide sequence, i.e., 5'-3' or 3'-5', is not critical to its function. Thus, enhancer sequences (e.g., E1-E10, e.g., E2, PV-specific enhancer sequences, or E5 or E6 described herein) may be used in the reverse orientation or as reverse complementary sequences. A "PV-specific enhancer" refers to an enhancer sequence described herein that targets and restricts transgene expression to PV-expressing cortical interneurons (PV-cINs) as described herein.

[0217] Furthermore, the enhancer does not need to be positioned at a specific distance relative to other sequences, such as the SCN1A coding sequence. Furthermore, the rAAV polynucleotide may contain additional elements, such as a reporter or detectable marker, such as a fluorescent protein, or an element that may enhance RNA stability and protein yield, such as the Woodchuck Hepatitis Virus Posttranscriptional Regulatory Element (WPRE). The rAAV polynucleotide may also contain a promoter for transcribing one or more polynucleotides (genes) inserted between the inverted terminal repeats (ITRs). A polyadenylation signal, such as a bovine growth hormone polyadenylation signal and / or an SV40 polyomavirus / simian virus 40 polyadenylation signal, may be included as an element in the rAAV polynucleotide. The rAAV polynucleotide can contain a minimal promoter, such as the human β-globin minimal promoter (phβg), and a chimeric intron sequence (Hermeming et al., 2004, J Virol Methods, 122(1):73-77). Without wishing to be bound by theory, the ITRs may aid in the formation of concatemers in the nucleus after the single-stranded AAV vector DNA is converted into double-stranded (ds) DNA by the host cell DNA polymerase complex. Thus, administration of the described rAAV may result in the formation of episomal concatemers in the nuclei of transduced interneuron cells. In non-dividing cells, such as adult interneurons, the concatemers may remain intact in these cells throughout the life of the interneuron. Advantageously, integration of the rAAV polynucleotide into host chromosomes is likely minimal or nonexistent and does not alter or affect the expression or regulation of any other human genes.

[0218] Recombinant AAV vectors can be produced using standard and well-established techniques in the art and commercially available reagents. It is understood by those skilled in the art that rAAV vectors used in several clinical trials have shown promising results. For example, as reported by Kotterman, MA et al., 2014, Nat. Rev. Genet., 15:445-451, rAAV-based therapy received marketing approval in the European Union in 2012. In some embodiments, the plasmid vector may encode all or part of the well-known replication (rep), capsid (cap), and adeno-helper components. The rep component contains four overlapping genes encoding Rep proteins (e.g., Rep78, Rep68, Rep52, and Rep40) required for the AAV life cycle. The cap component contains overlapping nucleotide sequences of capsid proteins VP1, VP2, and VP3, which interact together to form a capsid with icosahedral symmetry. A second plasmid encoding helper components, including the adenoviral genes E2A, E4orf6, and VA RNA for viral replication, can also be introduced into cells by co-transfection to provide helper functions to the AAV vector.

[0219] In one aspect, the method for producing rAAV for the products, compositions, and uses described herein includes culturing cells containing the rAAV polynucleotide expression vector as described; culturing the cells so that the polynucleotide can be expressed, producing rAAV in the cells, and separating or isolating the rAAV from the cells in the cell culture and / or cell culture medium. Such methods are known to and can be performed by those skilled in the art. rAAV can be purified from the cells and cell culture medium to any desired degree of purity using conventional techniques.

[0220] In one embodiment, the rAAV vector contains an SCN1A-restricted enhancer polynucleotide sequence and a sequence encoding a chemical genetic DREADD ("designer receptor exclusively activated by designer drugs"), such as a Gq-DREADD receptor (Hu, J. et al., 2016, J Biol Chem, 291:7809-7820). The amino acid sequence of the Gq-DREADD receptor is reported by Armbruster et al. (2007, Proc Natl Acad Sci USA, 104:5163-5168). The amino acid sequence of the Gq-DREADD receptor is a derivative of the amino acid sequence of the human muscarinic acetylcholine receptor, M3, in which the tyrosine at position 149 is replaced by a cysteine and the arginine at position 239 is replaced by a glycine. The unmodified human sequence is provided under NCBI accession number NP000731.1. In one embodiment, the polynucleotide sequence encoding the Gq-DREADD receptor in the rAAV vector can be modified, for example, by including codons optimized for expression of the Gq-DREADD receptor in human interneurons.

[0221] In one embodiment, the rAAV vector contains an SCN1A regulatory enhancer polynucleotide sequence and a sequence encoding a chemogenetic PSAM.

[0222] Recombinant AAV vectors have small genomes (approximately 5 kb) and can be engineered to package and contain larger genomes (transgenes), e.g., genomes larger than 4.7 kb. For example, two approaches developed to package large amounts of genetic material (genes, polynucleotides, nucleic acids) include split AAV vectors and fragment AAV (fAAV) genome reassembly (Hirsch, ML et al., 2010, Mol Ther 18(1):6-8; Hirsch, ML et al., 2016, Methods Mol Biol, 1382:21-39). Split rAAV vector applications have been developed to take advantage of the fact that rAAV genomes naturally concatenate within cells after transduction and are substrates for enhanced homologous recombination (HR) (Hirsch, ML et al., 2016, Methods Mol Biol, 1382:21-39). This approach involves "splitting" a large transgene into two separate vectors, which, when co-transduced, allow for reconstitution of the large gene within cells via vector genome concatenation via HR or non-homologous end joining (NHEJ). Generally, there are three strategies for split rAAV approaches: overlapping, trans-splicing, and hybrid trans-splicing.

[0223] Fragmented AAV (fAAV) as an approach for AAV-mediated large gene delivery was developed based on reports that attempted encapsidation of transgenic cassettes exceeding the packaging capacity of the AAV capsid resulted in packaging of heterogeneous single-stranded genomic fragments (<5 kb) of both polarities. After transduction of multiple fAAV particles, the genomic fragments can undergo opposite-strand annealing, followed by host-mediated DNA synthesis to reassemble the desired large genome intracellularly. (Hirsch, ML et al., 2016, Methods Mol Biol, 1382:21-39)

[0224] An advantage and benefit of the vectors, compositions, and methods described herein is the identification and use of sufficiently small enhancer elements (cis-acting elements) that can specifically restrict gene expression to a defined cell population, e.g., interneuron cells. In one embodiment, the enhancer element is at least one of the E1-E10 enhancer sequences described herein that is SCN1A-specific and restricts gene expression, e.g., the SCN1A gene, to interneuron cells, e.g., GABAergic interneurons and PV-expressing GABAergic interneurons, or pyramidal neurons, e.g., glutamatergic pyramidal neurons. The gene (transgene) delivered by the rAAV vector described herein is active, functional, and expressed in a specific cell, i.e., the product encoded by the gene (transgene) is produced and functionally expressed by the cell. As a specific example, the rAAV vectors described herein that have been engineered to contain enhancer sequences that specifically restrict expression of a transgene, e.g., a reporter gene or SCN1A, to GABAergic interneuron cells or GABAergic PV-expressing cortical interneuron cells, transduce these specific cell types, and the encoded reporter protein, or in the case of SCN1A, the Nav1.1 sodium channel, is functionally expressed in the specific cell types. As another specific example, the rAAV vectors described herein have been engineered to contain enhancer sequences that specifically restrict expression of a transgene, e.g., a reporter gene or SCN1A, to pyramidal cells, e.g., glutamatergic pyramidal cells, in the brain cortex.

[0225] Another advantage is that the described SCN1A-specific enhancer regulatory elements E1-E10 are small enough in size / length (e.g., less than about 2 kb) to be inserted into rAAV vectors along with other effector element polynucleotide sequences, such as reporter polynucleotides, DREADDs, and transgenes. For example, assuming the minimum size of essential reporter elements (e.g., enhanced green fluorescent protein (EGFP) or orange fluorescent protein (dTomato)) alone or in combination with effector or reporter elements (e.g., channelrhodopsin (ChR2) or DREADDs) averages about 700 bp to 2 kb, respectively, this leaves up to about 2 kb of packaging capacity remaining for insertion of cis-acting DNA regulatory elements, such as enhancer sequences, into rAAV vectors. The SCN1A-restricted enhancer sequences identified and described herein can restrict expression to defined cell populations, such as interneurons or GABAergic interneurons, or pyramidal neuron cells, and are small enough that additional nucleic acid sequences, reporter elements, and transgenes can also be cloned into the AAV vector.

[0226] Cell-specific AAV capsid Rational design of AAV vectors that exhibit selective tissue / organ targeting has broadened the application of AAV as a vector / vehicle for gene therapy. Both direct and indirect targeting approaches have been used to enhance the cell targeting specificity and retargeting of AAV vectors. For example, in direct targeting, AAV vector targeting to a specific cell type is mediated by a small peptide or ligand inserted directly into the viral capsid sequence. This approach has been successfully used to target endothelial cells. Direct targeting requires detailed knowledge of the capsid structure so that the peptide or ligand is positioned at a site exposed on the capsid surface. The insertion does not significantly affect capsid structure and assembly, and natural affinity is removed to maximize targeting to specific cell types. In indirect targeting, AAV vector targeting is mediated by a binding molecule that interacts with both the viral surface and a specific cell surface receptor. For AAV vectors, such binding molecules can include bispecific antibodies and biotin. The advantage of indirect targeting is that various adapters can be attached to the capsid without significantly altering the capsid structure, allowing for easy removal of natural affinities. Disadvantages of using adapters for targeting include the potential for reduced stability of the capsid-adapter complex in vivo.

[0227] Furthermore, AAV vectors containing capsids that enhance cell transduction and gene transfer to the central nervous system and brain via the vasculature can be produced. (Chan, KY et al., 2017, Nat. Neurosci., 20(8):1172-1179) Such vectors facilitate robust transduction of neuronal cells, including interneurons. When used with enhancers and cell-type-specific promoters, such AAVs can induce target gene expression in neuronal cells of the nervous system.

[0228] For applications that do not require high expression levels per cell, the amount of virus used, i.e., the viral dose, can be reduced. Using a lower viral load for systemic gene delivery reduces costs and manufacturing burdens and minimizes the potential risk of adverse reactions to the viral component.

[0229] Recombinant adeno-associated viral vector delivery and treatment approaches Generally, the delivery of effector genes for treating neurological diseases, for example, by modifying or correcting gene expression at the gene level, for example, by gene therapy, can be achieved using suitable and effective vectors, for example, viruses or viral vectors, for example, AAV or rAAV.The use of rAAV vectors effectively delivers therapeutic genes to the cells where the genes are expressed.Other methods and approaches for delivering genes to cells involve the use of purified DNA under hydrodynamic pressure, for example, DNA attached to gold particles or the shotgun approach using lipid-DNA complexes, but these methods and approaches often do not efficiently deliver genes, resulting in gene expression that is less than that required for therapeutic efficacy.In addition, these methods cannot be applied to human use.On the other hand, viruses are the natural carriers for delivering and expressing exogenous genes in host cells in vivo.

[0230] An advantage associated with the use of rAAV as a viral vector is that rAAV transgene expression typically persists for years or even lifelong periods, as demonstrated in animal models, in contrast to non-rAAV viral vectors, where transgene expression often has an initial burst that usually fades after a relatively short time, e.g., a few weeks.

[0231] To achieve enhanced therapy or treatment, the dose of rAAV vector required for a therapeutic response may be reduced, for example, by using certain rAAV serotypes. Alternatively, the surface of the rAAV vector capsid may be modified to contain specific ligands for attachment to target tissues and cells, as described above. Another approach considers the transport of viral particles from endocytoplasmic vesicles to the nucleus (Zhao, W. et al., 2007, Gene Ther., 14:545-550; Daya, S. and Berns, KI, 2008, Clin. Microbiol. Rev., 21(4):583-593). Typically, the viral particle-to-infectivity ratio of rAAV vector preparations is 10:1 to 100:1. This high ratio reflects incomplete or empty vector particles as well as transport from endoplasmic vesicles to the nucleus. During transport, vector particles can become ubiquitinated and be targeted to the proteasome for degradation rather than to the nucleus where the transgene can be expressed. It has been discovered that phosphorylation of tyrosine residues on the surface of the rAAV vector capsid is required for ubiquitination and targeting to the proteasome. When seven tyrosine residues on the surface of the AAV-2 capsid were replaced with phenylalanine residues, the multiplicity of infection (MOI) required for detection of transgene expression was significantly reduced in cell culture and in several mouse models of transduction of liver and eye cells. This may enhance the ability to increase transgene expression to therapeutic levels in the treatment of disease.

[0232] One or more treatment approaches for keeping seizures under control are included in the therapeutic products, compositions, and methods described herein, which involve cutting-edge gene therapy or pharmacogenetic approaches, which are likely to lead to the development of clinically relevant therapies for alleviating seizure symptoms in DS.

[0233] For direct delivery to the brain, rAAV vectors may be administered by open neurosurgical procedures or by local injection to bypass the blood-brain barrier, to restrict transgene expression temporally and spatially, and to target specific brain regions, such as interneuron cells and brain tissues containing these cells.

[0234] Systemic rAAV delivery (via intravenous injection) offers a noninvasive alternative for broad gene delivery to the nervous system. However, the required high viral load and relatively low transduction efficiency have limited the widespread adoption of this method. Several groups have developed rAAV capsids that enhance gene transfer to the CNS and certain tissues and cell populations after intravenous delivery. For example, the AAV-AS capsid18 utilizes a polyalanine N-terminal extension to the AAV9.4719VP2 capsid protein to enhance neuronal transduction, particularly in the striatum. The AAV2-based AV-BR1 capsid20 may be useful for efficient and selective transduction of brain endothelial cells. Another AAV capsid, AAV-PHP.B, contains a capsid that transduces the majority of neurons and astrocytes across many regions of the adult mouse brain and spinal cord after intravenous injection. In one embodiment, the rAAV comprises a capsid that specifically transduces interneurons, including PV interneurons, in the cerebral cortex (brain).

[0235] Other rAAV vector administration methods may include lipid-mediated vector delivery, hydrodynamic delivery, and gene guns. In certain embodiments, the rAAV vector comprises a capsid that increases the likelihood of directly infecting or transducing interneuron cells, such as GABAergic interneuron cells and GABAergic PV-expressing interneuron cells, or pyramidal cells, such as glutamatergic pyramidal cells, and brain tissues containing these cells.

[0236] The viral vectors and compositions described herein may be used in the treatment of neurological, neurodevelopmental, and neurodegenerative diseases and disorders, particularly epilepsy and its associated symptoms, including DS, which often includes severe seizure symptoms. A distinguishing feature between seizure categories is whether the seizure activity is partial (e.g., focal) or generalized. In one embodiment, the viral vectors and compositions described herein are used to treat partial and / or generalized seizures. Partial seizures are typically considered to be those in which seizure activity is restricted to a discrete cortical region. As will be understood by those skilled in the art, a seizure is characterized as a simple partial seizure if consciousness is fully maintained during the seizure. If consciousness is impaired, the seizure is characterized as a complex partial seizure. Complex partial seizures also include those that begin as a partial seizure and then spread throughout the cortex. Thus, these types of seizures are considered partial seizures with secondary generalization.

[0237] Generalized seizures involve distant brain regions simultaneously and bilaterally. For example, absence or petit mal seizures may involve a sudden, brief loss of consciousness without loss of postural control. Atypical absence seizures usually involve a longer loss of consciousness and a more gradual onset and end. Generalized tonic-clonic or grand mal seizures are considered the primary type of generalized seizure and typically occur suddenly and without warning. The initial phase of the seizure is usually accompanied by tonic muscle contractions and a marked increase in sympathetic tone, leading to respiratory disturbances and dilated heart rate, blood pressure, and pupil size. After approximately 10–20 seconds, the tonic phase of the seizure typically evolves into a clonus phase, which is typically caused by periods of muscle relaxation superimposed on the tonic muscle contractions. The relaxation periods progressively increase until the end of the seizure phase, which usually lasts less than one minute. The postictal phase is characterized by unresponsiveness, muscle atonia, and excessive salivation that can lead to wheezing breathing and partial airway obstruction.

[0238] Atonic seizures are characterized by a sudden loss of postural muscle tone lasting approximately 1-2 seconds. During the brief loss of consciousness, there is usually no postictal confusion. Myoclonic seizures are characterized by sudden, brief muscle contractions that may involve one or the entire body. Without limitation, the rAAV products, compositions, and methods of use described herein include the prophylactic and / or therapeutic treatment of seizures, including those afflicting individuals with DS. In one embodiment, the rAAV products, compositions, and methods of use described herein are used for the prophylactic and / or therapeutic treatment of epilepsy associated with loss of or impaired function of the sodium channel Nav1.1, encoded by the SCN1A gene. In a specific embodiment, the rAAV products, compositions, and methods of use described herein are used for the prophylactic and / or therapeutic treatment of Dravet syndrome (DS). In another embodiment, the rAAV products, compositions, and methods of use described herein are used for the prophylactic and / or therapeutic treatment of drug-resistant epilepsy. Drug-resistant epilepsy refers to an epileptic condition that is not controlled despite the use of two or more drugs that are suitable for treating this type of epilepsy and are administered at maximum tolerated doses (MTDs). In embodiments, drug-resistant epilepsy encompasses a condition in which a previous antiepileptic drug treatment or combination of treatments has not resulted in seizure freedom.

[0239] Pharmacogenetic approach Pharmacogenetic approaches are being considered for use with the viral vectors, rAAV vectors, compositions thereof, and methods described herein. Such approaches use viral vectors, e.g., rAAV vectors, containing the enhancer elements (e.g., E1-E10) described herein and a polynucleotide encoding a Gq-DREADD receptor or PSAM to specifically deliver the Gq-DREADD receptor or PSAM to PV interneurons. The targeted PV neurons stably express the receptor (Gq-DREADD or PSAM) in a specific region via local injection, as determined by the type of pathology being treated, or throughout the cortex via systemic injection. The individual (patient) is then administered a drug that activates the receptor (e.g., CNO or PSEM, respectively). This approach results in controlled changes in the excitability of PV interneurons expressing the receptor, modulating the excitation / inhibition (E / I) balance in neurons (interneurons and PV-expressing interneurons) in a dose- and time-dependent manner, resulting in normalization of brain activity.

[0240] Pharmaceutical Compositions Also provided is a pharmaceutical composition or formulation for treating subjects suffering from or at risk of developing neurological or neurodevelopmental diseases, disorders, or conditions, such as DS.In one embodiment, the pharmaceutical composition comprises (as an active agent) an AAV vector or viral particle, for example, an AAV vector or viral particle containing the SCN1A-specific enhancer sequence described herein, and a pharmaceutically acceptable carrier, excipient, or diluent.When formulated into a pharmaceutical composition, the rAAV vector as a therapeutic compound or product can be mixed with a pharmaceutically acceptable carrier, diluent, or excipient.

[0241] The therapeutic agent can be contained in any suitable amount in any suitable carrier material, generally in an amount of 1-95% by weight based on the total weight of the composition. The composition may be provided in a dosage form suitable for parenteral (e.g., subcutaneous, intravenous, intramuscular, or intraperitoneal) administration, so that agents such as the viral vectors described herein can be delivered systemically. In one embodiment, systemic injection of the rAAV vectors described herein allows for characterization of expression specificity across brain regions, particularly when a reporter product is also encoded by the vector. Pharmaceutical compositions can be formulated according to conventional pharmaceutical practice (see, e.g., Remington: The Science and Practice of Pharmacy (20th ed.), ed. A.R. Gennaro, Lippincott Williams & Wilkins, 2000 and Encyclopedia of Pharmaceutical Technology, eds. J. Swarbrick and J.C. Boylan, 1988-1999, Marcel Dekker, New York).

[0242] Pharmaceutical compositions can be formulated to release the active agent more or less immediately upon administration, or at any predetermined time or time after administration. The latter type of composition is commonly known as a controlled release formulation, which includes: (i) formulations that produce a substantially constant drug concentration in the body over an extended period of time; (ii) formulations that produce a substantially constant drug concentration in the body over an extended period of time after a predetermined lag time; (iii) formulations that sustain action for a predetermined period of time by maintaining a relatively constant effective level in the body, concomitantly minimizing undesirable side effects associated with fluctuations in plasma levels of the active agent (sawtooth kinetic pattern); and (iv) formulations that release the active agent at a predetermined time, e.g., adjacent to or in contact with a target site or location. These include formulations that localize the effect to, for example, a tissue or organ region by spatial arrangement of the controlled-release composition, (v) formulations that allow convenient dosing, such as administering a dose once every week, every two weeks, or every few weeks, and (vi) formulations that target specific tissues or cell types using carriers, chemical derivatives, or specially designed vectors (e.g., containing certain capsid compositions) to deliver a therapeutic agent to, for example, interneurons, or PV-expressing GABAergic interneurons, or pyramidal neurons, e.g., glutamatergic pyramidal neurons. For some applications, controlled-release formulations eliminate the need for frequent daytime dosing to maintain therapeutic plasma levels of the administered agent.

[0243] Methods for obtaining controlled release, in which the release rate exceeds the metabolic rate of the drug in question, are not intended to be limiting. For example, controlled release can be obtained by appropriately selecting various formulation parameters and ingredients, including, for example, various types of controlled-release compositions and coatings. Thus, therapeutic agents are formulated with appropriate excipients into pharmaceutical compositions that, upon administration, controllably release the drug. Examples include single- or multiple-unit tablet or capsule compositions, oil solutions, suspensions, emulsions, microcapsules, microspheres, molecular complexes, nanoparticles, patches, and liposomes.

[0244] Administration of a composition comprising a combination of agents for treating a neurological disease or disorder, such as DS, may be by any suitable means that, when combined with other components, results in a concentration of the therapeutic agent effective to ameliorate, alleviate, reduce, diminish, or stabilize seizures in a subject. The composition may be formulated and administered systemically, for example, in a pharmaceutically acceptable buffer, such as saline. In one embodiment, systemic injection of the rAAV vectors described herein allows for characterization of expression specificity across brain regions, particularly when a reporter product is also encoded by the vector.

[0245] Routes of administration include, for example, intracranial, parenteral, subcutaneous (sc), intravenous (iv), intraperitoneal (ip), intramuscular (im), or intradermal administration, e.g., by injection, optimally providing continuous, sustained levels of the agent in the patient. The amount of therapeutic agent administered will vary depending on the method of administration, the patient's age, physical condition, and weight, and the clinical symptoms of the neurological disease or disorder, such as DS. Generally, amounts will be in the range of those used for other viral vector-based agents used in the treatment of neurological diseases or disorders, particularly in the brain; however, in some cases, lower amounts may be required if the agent exhibits high specificity. The composition is administered at a dosage that exhibits a therapeutic effect, e.g., an effect of ameliorating, alleviating, reducing, diminishing, or stabilizing seizures in the patient, as determined by methods known to those skilled in the art.

[0246] Pharmaceutical compositions may be administered parenterally by injection, infusion, or implantation (subcutaneous, intravenous, intramuscular, intraperitoneal, intracranial, etc.) in the form of a dosage form, formulation, or via a suitable delivery device or implant containing conventional non-toxic pharmaceutically acceptable carriers and adjuvants. The formulation and preparation of such compositions are well known to those skilled in the art of pharmaceutical formulations and can be found, for example, in Remington: The Science and Practice of Pharmacy, supra. In certain embodiments, administration is systemic administration and parenteral administration, for example, by injection or intravenous delivery.

[0247] Compositions for parenteral delivery and administration may be provided in unit dosage form (e.g., in single-dose ampoules) or in vials containing several doses, to which appropriate preservatives may be added (see below). The compositions may take the form of a solution, suspension, emulsion, injection device, or implantable delivery device, or may be presented as a dry powder to be reconstituted with water or another suitable vehicle before use. In addition to the active agent (e.g., a viral vector or particle comprising an enhancer sequence and a polynucleotide encoding an effector gene and associated regulatory sequences, as described herein), the composition may contain suitable parenterally acceptable carriers and / or excipients. The active therapeutic agent may be incorporated into microspheres, microcapsules, nanoparticles, liposomes, etc. for controlled release. Additionally, the composition may contain suspending agents, solubilizing agents, stabilizing agents, pH adjusters, tonicity adjusters, and / or dispersing agents.

[0248] In some embodiments, compositions containing an active therapeutic agent (i.e., a viral vector or particle described herein) are formulated for intravenous delivery. As noted above, pharmaceutical compositions according to the described embodiments may be in a form suitable for sterile injection. To prepare such compositions, a suitable therapeutic agent is dissolved or suspended in a parenterally acceptable liquid vehicle. Acceptable vehicles and solvents that may be used include water, water adjusted to an appropriate pH by adding an appropriate amount of hydrochloric acid, sodium hydroxide, or an appropriate buffer, 1,3-butanediol, Ringer's solution, isotonic sodium chloride solution, and dextrose solution. Aqueous formulations may also contain one or more preservatives (e.g., methyl, ethyl, or n-propyl p-hydroxybenzoate). If one of the agents is sparingly or only slightly soluble in water, a dissolution-enhancing agent or solubilizer may be added, and the solvent may include 10-60% w / w propylene glycol, for example.

[0249] Methods of Administration and Delivery A viral vector or pharmaceutical composition described herein is administered to a subject with DS, e.g., a patient or infant patient. In some embodiments, the viral vector, viral particle, or pharmaceutical composition can be delivered to cells (e.g., target cells, e.g., interneurons or brain layers containing interneurons) in any manner that functions or is active in expressing the sequence contained in the vector or viral particle. Illustratively, an rAAV containing an SCN1A-specific enhancer and effector gene (e.g., SCN1A) polynucleotide sequence can be delivered to interneuron cells or tissues containing interneuron cells to target SCN1A expression in interneurons. Thus, the viral vector or viral particle is delivered to cells by contacting the cells with a composition containing the viral vector or viral particle, thereby heterologously expressing the polynucleotide contained in the viral vector or viral particle in the cells. To produce therapeutically effective levels of the encoded product, the polynucleotide contained in the rAAV vector must be delivered to the subject's cells in an internalized form.

[0250] Transducing rAAV vectors are used to deliver and express genes encoding desired proteins, polypeptides, or peptides into cells, particularly because of their high infection efficiency and stable integration and expression (see, e.g., Cayouette et al., Human Gene Therapy, 8:423-430, 1997; Kido et al., Current Eye Research, 15:833-844, 1996; Bloomer et al., Journal of Virology, 71:6641-6649, 1997; Naldini et al., Science, 272:263-267, 1996; and Miyoshi et al., Proc. Natl. Acad. Sci. USA, 94:10319, 1997). For example, rAAV can be engineered to include a polynucleotide encoding an SCN1A-specific enhancer nucleic acid sequence described herein, which preferentially induces gene expression in a specific interneuron cell type, and used to induce and restrict expression of a gene, e.g., SCN1A, to GABAergic interneuron target cells or pyramidal target cells, e.g., glutamatergic pyramidal cells. In one embodiment, the gene can be expressed from any suitable promoter, such as a target cell-specific promoter. In one embodiment, the rAAV vector is administered systemically. In one embodiment, systemic injection of the rAAV vector described herein allows for characterization of expression specificity across brain regions, particularly when, for example, a reporter product is also encoded by the vector.

[0251] Gene transfer can also be achieved using in vitro transfection methods, including the use of calcium phosphate, DEAE-dextran, electroporation, and protoplast fusion. Liposomes can also be potentially useful for delivering DNA into cells.

[0252] Treatment Methods and Protocols Methods of administering a therapeutic agent to a subject in need thereof, such as a subject having, experiencing, having experienced, and / or at risk of experiencing a neurological disease or disorder, more particularly, seizures, epilepsy, or DS, as well as to a subject who may be diagnosed with, suspected of having, or suspected of having symptoms of a seizure disorder, or to a subject identified as needing such treatment, are provided, in which an effective amount of a viral vector or viral particle described herein or a composition described herein is administered to the subject to produce a therapeutic effect. According to the described methods, the therapeutic effect includes, but is not limited to, an amount of rAAV introduced into a sufficient number of interneurons after administering the rAAV vector product or composition to the subject to inhibit, reduce, or ameliorate one or more symptoms of a neurological disease or disorder, such as seizures or epilepsy, or to prevent one or more symptoms. The amount of rAAV administered can be determined by one skilled in the art, e.g., a medical or clinical professional, and is based on factors such as the size of the epileptic lesion, the titer of the viral preparation, and data obtained in non-human primates, as understood by those skilled in the art (e.g., Colle, M.-A. et al., 2010, Hum. Mol. Genet., 19:147-158). For example, 10 to 10 rAAV vectors or particles thereof can be administered to transduce a therapeutically relevant number of interneurons. 10 ~10 12 Identification of a subject in need of such treatment may be at the discretion of the subject or a health care professional and may be subjective (e.g., opinion) or objective (e.g., measurable by a test or diagnostic method).

[0253] Therapeutic methods (including prophylactic treatments) generally involve administering a therapeutically effective amount of an agent described herein, such as an rAAV vector, viral particle, or composition containing the agent, to a subject (e.g., animal, human) in need thereof, including a mammal, particularly a human. Such treatments are suitably administered to subjects, particularly humans or infant humans, who suffer from, have, are susceptible to, or are at risk for a neurological disease or disorder, such as seizures and / or epilepsy, or DS. The determination of a subject "at risk" can be made by diagnostic testing or any objective or subjective determination (e.g., genetic testing, enzyme or protein markers or biomarkers, family history, etc.) based on the subject's or a healthcare provider's opinion.

[0254] The viral vectors and pharmaceutical compositions as described may be used therapeutically to treat patients suffering from a neurological or neurodegenerative disease or disorder, such as seizures, epilepsy, or DS, or may be used prophylactically to provide advanced treatment or protection to patients at risk for certain neurological or neurodegenerative diseases or disorders, such as prophylactic vaccination to reduce, diminish, alleviate, or avoid one or more symptoms or the severity of seizures, epilepsy, or DS. The prophylactically effective amount of the rAAV vectors described herein is not intended to be limiting herein and may be about 10 per kilogram of recipient body weight. 2 TU (transducing unit) ~ approximately 10 per kilogram of recipient body weight 20 The dose may be 100 mg / kg / day or any dose between these values. Mouse models of seizures and DS can be used to optimize dosages and regimens.

[0255] The therapeutic vectors described herein can be administered to a subject in need thereof in an amount effective to normalize the excitability of interneurons deficient in SCN1A and to reduce the seizures and seizure symptoms of Dravet syndrome (DS). The vectors and methods described herein may be of therapeutic value to individuals, e.g., human infants, children, or adults, who have experienced or are at risk of experiencing one or more seizures and / or DS. In one embodiment, the rAAV or a composition comprising an rAAV described herein is administered to an individual having interneurons that, upon administration, do not express or exhibit loss of function or expression of the SCN1A gene encoding the Nav1.1 sodium channel, which SCN1A gene depends on an SCN1A-specific enhancer, such as E1-E10, described herein, for expression. In one embodiment, expression of SCN1a in interneuron cells transduced with the described rAAV vectors containing an SCN1A-restricted enhancer sequence normalizes the excitability of interneurons that are deficient in SCN1A or have abnormal expression of SCN1A. In one embodiment, the composition comprising the rAAV vector described herein is administered to an individual with interneurons that no longer express SCN1A gene.In one embodiment, the composition comprising the rAAV vector described herein is administered to an individual that is at least 1 month old.In one embodiment, the individual is at least 1 year old, 2 years old, 3 years old, 4 years old, 5 years old, 6 years old, 7 years old, 8 years old, 9 years old, 10 years old, 11 years old, 12 years old, 13 years old, 14 years old, 15 years old, 16 years old, 17 years old or 18 years old.

[0256] Subjects, e.g., mammalian subjects and human patients, to whom the rAAV vectors described herein are administered may also benefit from adjunctive or additional treatments or therapeutic compounds or drugs, e.g., anti-seizure modalities, including, but not necessarily limited to, use with other anti-epileptic therapies and / or surgical techniques known to those skilled in the art. By way of example, antiepileptic drugs (AEDs) that may be used in conjunction with the therapeutic products and compositions described herein include, but are not limited to, acetazolamide, brivaracetam, carbamazepine, clobazam, clonazepam; eslicarbazepine acetate, ethosuximide, gabapentin, lacosamide, lamotrigine, levetiracetam, oxcarbazepine, perampanel, phenobarbital, phenytoin, pregabalin, primidone, rufinamide, sodium valproate, stiripentol, tiagabine, topiramate, valproic acid (available as Convulex, EpilimChrono, Epilim Chronosphere), vigabatrin, and zonisamide.

[0257] kit Also provided are kits for preventing or treating a neurological or neuropsychiatric disease, condition, or pathology, such as seizures and / or epilepsy, and the symptoms of Dravet syndrome (DS), in a subject in need thereof. In one embodiment, the kit is a therapeutic or prophylactic composition containing an effective amount of an rAAV vector or viral particle described herein, wherein the rAAV vector or viral particle described herein comprises an enhancer polynucleotide sequence specific to the SCN1A gene, e.g., the SCN1A gene contained in the viral vector, that restricts expression of the SCN1A gene to interneuron cells, including GABAergic interneuron cells, in the brain (i.e., the telencephalon), or to pyramidal cells, e.g., glutamatergic pyramidal cells, or VIP cells, in the brain cortex. In one embodiment, the SCN1A-specific enhancer is an E1, E2, E3, E4, E5, E6, E7, E8, E9, or E10 human enhancer sequence described herein. In one embodiment, the SCN1A-specific enhancer is an E2 human enhancer polynucleotide sequence. In one embodiment, the SCN1A-specific enhancer is an E5 human enhancer polynucleotide sequence. In one embodiment, the SCN1A-specific enhancer is an E6 human enhancer polynucleotide sequence.

[0258] In another aspect, the kit provides a therapeutic or prophylactic composition containing an effective amount of an rAAV vector or viral particle described herein, wherein the rAAV vector or viral particle described herein comprises an E11-E35 enhancer polynucleotide sequence, particularly a human E11-E35 sequence, specific for a gene expressed in a neuronal or interneuronal cell, particularly a PV-expressing neuron.

[0259] In some embodiments, the kit includes a sterile container containing the therapeutic or prophylactic composition. Such a container may be a box, an ampoule, a bottle, a vial, a tube, a bag, a pouch, a blister pack, or any other suitable container form known in the art. The container may be made of plastic, glass, laminated paper, metal foil, or other materials suitable for holding pharmaceuticals.

[0260] A composition comprising an rAAV vector comprising at least an SCN1A-specific enhancer polynucleotide sequence described herein is provided together with instructions for administering the composition to a subject with seizures, epilepsy, or DS, or at risk of developing seizures, epilepsy, or DS. In one embodiment, the rAAV vector comprises an SCN1A transgene for expression in interneuron cells, including GABAergic interneurons and PV-expressing interneurons, or pyramidal cells, such as glutamatergic pyramidal cells. The instructions generally include information about using the composition to treat or prevent seizures, epilepsy, or DS. In other embodiments, the instructions include at least one of the following: a description of the therapeutic agent (such as an rAAV comprising an SCN1A-specific enhancer polynucleotide sequence); a dosing regimen and administration for treating or preventing ischemia or its symptoms; precautions for use; warnings; indications; contraindications; overdose information; adverse reactions; animal pharmacology; clinical studies; and / or references. The instructions may be printed directly on the container (if present), as a label affixed to the container, or as a separate sheet, pamphlet, card, or folder provided in or with the container.

[0261] Further Aspects and Advantages Understanding and developing methods for treating neurological disorders derives from the complexity of the neuron types involved. The products and methods described herein were developed to analyze the cellular activity of disease genes or disease-associated genes. Accordingly, the SCN1A locus was systematically analyzed, identifying 10 distinct enhancer elements (enhancers E1-E10), specifically human enhancer elements and their sequences, which were found to be distributed throughout the intronic and intergenic regions of the SCN1A gene (Figure 3D). By creating AAVs whose expression is dependent on each of these enhancers, at least three enhancers were identified that recapitulate the overall pattern of SCN1A gene expression, such as E2 (for PV-specific expression), E6 (for VIP-specific expression), and E5 (for pyramidal layer 5-associated expression). The other seven elements (e.g., E1, E3, E4, E7, E8, E9, and E10) are all highly specific for GAD1 and can target a collection of interneuron subpopulations, recruiting distinct combinations of subtypes. In certain embodiments, the E2 enhancer element was found to be selective for a specific cIN subtype, namely, PV-expressing fast-spiking cells. Loss of SCN1A expression is particularly associated with PV cIN dysfunction, and the E2 enhancer proved particularly adept at selectively targeting this cell population in rodents as well as various primates, including humans. Furthermore, the E2 enhancer proved useful for investigating aspects of PV cIN function, including, but not limited to, monitoring connectivity, excitability, and manipulating PV cIN activity using optogenetics. The demonstrated utility of the E2 enhancer across a wide range of species highlights the breadth of basic and clinical applications offered by this approach. Other uses afforded by the E2 enhancer include, by way of example, broader circuit interrogation (e.g., generating starter cells for monosynaptic tracing using recombinant viruses such as rabies), cell type-specific gene loss-of-function (e.g., CRISPR), and targeted drug screening.Furthermore, the use of E2 enhancers provides an agent for examining species-specific differences in the number, distribution, or physiological properties of PV cINs. When generalized to other cell types, this approach would be advantageous for examining a wide range of species, most notably primates and humans.

[0262] As described herein, a strategy to systematically interrogate enhancers at a specific disease locus, such as the SCN1A locus, successfully identifies key regulatory elements in each of the cell types that express this gene, thus highlighting the advantages of this approach: it reveals the regulatory signatures that control SCN1A gene expression and provides a toolkit for engineering distinct cell subpopulations that express the SCN1A gene.

[0263] Many of the SNPs associated with the SCN1A locus are located in intron 1. In a specific embodiment, and as described herein, three enhancers identified as having high specificity for the SCN1A-expressing population, namely E2, E5, and E6, were located within this region. Without wishing to be bound by theory, the identified SNPs may be mutations in these enhancers that affect SCN1A expression. GTEx data have reportedly shown multiple eQTLs within these enhancers that are associated with altered SCN1A expression in humans (Auget, F. et al., 2017, Nature, 550:204-213). E2 is of particular interest because conditional deletion of SCN1A from forebrain interneurons has been shown to recapitulate seizure phenotypes in mice. Because SCN1A expression is primarily restricted to the PV-expressing subpopulation of interneurons, mutations in the E2 enhancer may be the direct cause of Dravet syndrome.

[0264] One of the biggest obstacles to investigating the early dynamics of circuit maturation has been the limited accessibility of specific cell types without the use of transgenic animals. Young PV cINs have been particularly challenging to target, even with complex genetic strategies. Given the abundance of PV-cINs (representing 40% of all inhibitory cINs) and their involvement in neurodevelopmental disorders, assessing these cells before the onset of PV expression is a priority for the field. The specificity of the E2 enhancer and the use of viral injections at these developmental stages provide agents and tools for understanding the normal development of neuronal cell types, such as PV cINs, and their role in neurological or neuropsychiatric disorders. In one aspect, the E2 enhancer provides agents for studying the normal development of PV-cINs and their role in disease. Furthermore, the E2 enhancer, as well as other enhancer elements provided herein, may be useful for targeting specific cells, which would be advantageous for treating neuronal disorders, including Labé syndrome.

[0265] In other aspects, the enhancers identified and described herein provide access to specific cell populations with distinct clinical relevance. For example, these enhancers can be used to alleviate the debilitating aspects of Dravet syndrome, for example, by gene therapy or through modulation of neuronal activity, e.g., via optogenetic or chemogenetic approaches (see, e.g., Walker, MC et al., 2019, Neuropharmacology, 107751. doi: 10.1016 / j.neuropharm.2019.107751. Review. PMID: 31494141). As described and demonstrated herein, local and systemic injections can be used for effective viral delivery to the brain, thus providing delivery and administration methods for clinical intervention. For example, local injections (e.g., local injections of recombinant viruses carrying enhancer elements and target polynucleotides) can be used to alleviate focal epilepsy, prefrontal cortical dysfunction, or hippocampal memory impairment. Systemic administration or delivery of viruses may be used in situations where global intervention is required, for example, to correct generalized seizures or psychiatric and neurodegenerative disorders.As provided by the embodiments described and exemplified herein, precise identification of regulatory elements allows for the evaluation of specific cell types.Such elements are advantageous for use in both experimental and therapeutic procedures and methods.

[0266] The practice of the described embodiments employs, unless otherwise specified, conventional techniques of molecular biology (including recombinant methods), microbiology, cell biology, biochemistry, and immunology, which are well within the skill of those in the art. Such techniques are fully explained in the literature, for example, "Molecular Cloning: A Laboratory Manual," 2nd Edition (Sambrook, 1989); "Oligonucleotide Synthesis" (Gait, 1984); "Animal Cell Culture" (Freshney, 1987); "Methods in Enzymology" and "Handbook of Experimental Immunology" (Weir, 1996); "Gene Transfer Vectors for Mammalian Cells" (Miller and Calos, 1987); "Current Protocols in Molecular Biology" (Ausubel, 1987); "PCR: The Polymerase Chain Reaction" (Mullis, 1994); and "Current Protocols in Immunology" (Coligan, 1991). These techniques are applicable to the production of polynucleotides, viral vectors, and viral particles, and therefore may be considered in making and practicing the embodiments described herein. Techniques that are particularly useful for particular embodiments are discussed in the following sections.

[0267] The following examples are put forth so as to fully disclose and describe to one of ordinary skill in the art how to make and use the products, compositions, and treatment methods described herein, and are not intended to limit the scope of what is described and exemplified herein. [Example]

[0268] Example 1 - Identification of cis-regulatory sequences (PV interneuron-specific enhancer sequences) that restrict reporter and effector gene expression to the PV-expressing cortical interneuron cell population SCN1A is a gene encoding the Nav1.1 sodium channel and is expressed in multiple distinct neuronal populations in the cortex. These include three non-overlapping neuronal populations: parvalbumin-expressing fast-spiking cortical interneurons (PV cINs), vasoactive intestinal peptide-expressing disinhibited cortical interneurons (VIP cINs), and layer 5 pyramidal neurons. In certain embodiments, SCN1A is expressed in PV-expressing cortical interneurons. SCN1A is of particular interest because its loss of function is associated with Dravet syndrome, an early-onset and intractable epileptic encephalopathy characterized by early onset of seizures. More specifically, haploinsufficient or pathogenic variants of SCN1A cause Dravet syndrome.

[0269] An integrated approach to systematically identify candidate enhancers within the SCN1A locus was developed and devised as a genetic strategy for targeting distinct cortical populations expressing this gene. Regulatory sequences were selected based on three criteria. First, because it has been determined that the proximity of an enhancer to a gene's transcription start site (TSS) is directly proportional to its expression level, we examined the intergenic and intronic regions of SCN1A closest to the TSS to identify enhancers capable of driving functional levels of the transgene. Second, because the location of active enhancers within a given cell type correlates with chromatin accessibility, we used Dlx6a to assess the chromatin properties of SCN1A-expressing cell populations. cre Interneurons were collected from the visual cortex using Sun1-eGFP transgenic mice, and the location of active enhancers in a given cell type correlated with chromatin accessibility and DNA hypomethylation.

[0270] After isolating nuclei, we performed single-cell ATAC-seq profiling (see, e.g., Buenrostro, JD et al., Nature, 523:486-90 (2015) and Cusanovich, DA et al., Science, 348:910-4 (2015)) using the SnapATAC analysis pipeline (described in Methods below) to identify differentially accessible chromatin regions in each of the four major classes of cortical interneurons, including PV cINs, VIP cINs, and pyramidal neurons, which express the highest levels of SCN1A (Figures 3A-3C and 12). Third, because regulatory elements are subject to positive selection pressure, we identified sequences that show the highest conservation across mammalian species, including humans. Therefore, to identify and isolate enhancers with therapeutic potential, we evaluated 10 selectively accessible intronic and intergenic regions near the TSS of SCN1A that are highly conserved throughout evolution, e.g., E1-E10 described herein (Figure 3D and Figures 15A-1, 15A-2, 16A-1, and 16A-2).

[0271] To test the ability of candidate enhancers to target SCN1A-expressing neuronal populations, we inserted each enhancer sequence into a rAAV backbone (rAAV-E[x]-dTomato) containing a minimal promoter upstream of a red fluorescent reporter. These constructs were then used to generate rAAVs with PHPeB capsids (Chan, KY et al., Nat. Neurosci., 20:1172-1179 (2017)) and injected systemically into adult mice. Three weeks later, all viruses showed strong but sparse expression within the cortex and across multiple brain regions. With the exception of E5, the majority of virus-labeled cells expressed the pan-interneuron marker Gad1. However, the degree of colocalization with PVs within cortical neurons varied, ranging from over 90% for E2 to less than 5% for E6, with all remaining enhancers exhibiting intermediate levels of PV specificity (Figure 3E and Figure 7). We then further investigated the identity and layer distribution of the neuronal populations captured by the E2, E5, and E6 enhancers. Consistent with the layer distribution, colocalization analysis using various markers revealed that the E2 regulatory element restricted viral reporter expression to PV cINs, whereas E6 was selective for VIP interneurons. In contrast, the E5 regulatory element sparsely labeled interneurons across all layers but was particularly abundant in pyramidal neurons in layer 5 (Figure 3F). Thus, a significant proportion of the cortical expression profile of SCN1A was reflected by the collective expression of the three enhancers. Thus, these regulatory elements account for the largely nonoverlapping expression in interneurons as well as in populations of neurons with distinct functions and developmental origins. The viral tools developed as described herein provide a means for analyzing neuronal subtypes and can be advantageously used to study their normal function as well as abnormalities in the diseased cortex.

[0272] In a specific aspect, we incorporated the S5E2 (E2) enhancer element sequence into a recombinant AAV (rAAV) vector containing a minimal basic promoter and a reporter transgene (e.g., d-Tomato) or effector gene (e.g., Gq-DREADD) to create a rAAV vector called pAAV-S5-E2-dTomato. The ability of the E2 enhancer to restrict reporter gene (transgene) expression to PV-expressing interneurons in the brain was assessed by systemically injecting mice with the E2 enhancer-containing rAAV vector and analyzing the colocalization of the expressed reporter across brain structures, including the cortex. Images showing the results of immunohistochemical (IHC) staining analysis for the dTomato reporter in brain sections after systemic in vivo injection of mice with the pAAV-S5-E2-dTomato vector, which allows for the detection of specific cells transduced by the vector, are shown in Figure 2A (sagittal sections at the top of the figure; coronal sections at the bottom of the figure). Figure 2B shows images showing the results of immunohistochemical (IHC) staining analysis for the expressed dTomato reporter in brain sections after systemic in vivo injection of the pAAV-S5-E2-dTomato vector into mice, enabling the detection of specific PV-expressing cells. Reporter gene expression from the pAAV-S5-E2-dTomato vector was visualized in brain sections (Figure 2B, left panel, red). Reporter gene expression from pAAV-S5-E2-Gq-DREADD-dTomato was visualized for Gq-DREADD (green) and dTomato (red) (Figure 2B, right panel). Detection of specific PV-expressing cells transduced by the vector was also visualized (Figure 2B, left panel, green; Figure 2B, right panel, blue).

[0273] Identification of candidate enhancers Using the enhancer sequence selection approach described above, 10 candidate enhancer sequences near the SCN1A gene transcription start site were observed in the mouse genome. These enhancer sequences, designated herein as S5E1 (E1), S5E2 (E2), S5E3 (E3), S5E4 (E4), S5E5 (E5), S5E6 (E6), S5E7 (E7), S5E8 (E8), S5E9 (E9), and S5E10 (E10), were identified near the SCN1A gene (Figure 1A-1). Human polynucleotide sequences corresponding to the E1-E10 enhancer sequences (SEQ ID NOS: 15-24) are also provided and described herein, and additional human enhancer polynucleotide sequences E11-E35 (SEQ ID NOS: 25-49) are also described herein (Figures 1A-2 and 1A-3).

[0274] The human (human ortholog) sequences of the E1-E10 enhancers were determined based on an alignment of the mouse and human genomic sequences of SCN1A, including 100 kb upstream and downstream. This identified a human ortholog sequence that is highly conserved between the two species (Figures 1A-1 to 1A-3, 16A-1, and 16A-2). As will be appreciated by those skilled in the art, enhancer regulatory elements contain a series of transcription binding sites that are relatively well conserved between species but are interspersed with spacer sequences that are not contiguous between species. Thus, in one embodiment, the SCN1A enhancer element may comprise a nucleotide sequence containing any region of greater than 100 bp that shares at least 75% sequence identity with the human polynucleotide (DNA) enhancer sequences described herein, i.e., E1-E10. In one embodiment, the SCN1A enhancer element comprises a nucleotide sequence containing any region greater than 100 bp that has at least 75% or greater sequence identity to the human E2 (S5E2) polynucleotide (DNA) enhancer sequence. For such enhancer sequences, the size of the nucleic acid sequence is not limited, so long as the sequence contains any region greater than 100 bp that has at least 75% or greater sequence identity to the human polynucleotide (DNA) E1-E10 or E11-E35 enhancer sequences described herein. Data associated with each of the identified enhancer sequences described herein (35 enhancer sequences) are provided in the tables set forth in Figures 1A-1-1A-3, 15A-1, 15A-2, 16A-1, and 16A-2.

[0275] Figures 1B-1 and 1B-2 show reporter gene expression restricted by the E1-E10 enhancer element in PV-expressing interneurons in the cortical layers of the mouse brain. These figures show immunohistochemical (IHC) staining analysis for dTomato in brain sections after systemic in vivo injection of the pAAV-S5-E2-dTomato vector into mice. Quantification of the degree of specificity (Figure 1C) and sensitivity (Figure 1D) of reporter gene expression in PV-expressing interneurons in the cortex is graphically demonstrated. Reporter gene expression is controlled by the E1-E10 enhancer element contained in the rAAV vector. Specificity was quantified as the percentage of cells expressing the viral reporter dTomato that co-express the PV interneuron marker PV, as assessed by immunohistochemistry on brain sections after systemic in vivo injection of the pAAV-S5-E2-dTomato vector into mice. Sensitivity was quantified as the percentage of cells expressing the PV interneuron marker PV that co-expressed the viral reporter dTomato, as assessed by immunohistochemistry on brain sections after systemic in vivo injection of pAAV-S5-E2-dTomato vector into mice. Bars represent the mean + / - standard error of the mean.

[0276] Example 2 - Viral targeting of PV cortical interneurons (PV cIns) in mice The 90% specificity of the E2 regulatory element for PV cINs provides a means for targeting fast-spiking neurons (e.g., basket cells and chandelier cells), which collectively comprise 40% of all cortical (GABAergic) interneurons. These neurons exert strong levels of inhibition across local networks, and their dysfunction has been directly implicated in neurological and neuropsychiatric disorders, including Dravet syndrome, focal epilepsy, autism spectrum disorder (ASD), and schizophrenia. Therefore, controlling their activity is of particular interest in both basic research and clinical applications. Therefore, we investigated and characterized the E2 regulatory element to develop drugs with broad utility, for example, as viral tools or therapeutic agents.

[0277] Adult mice systemically injected with rAAV-E2-dTomato showed detectable viral reporter expression after 1 week, reaching high and stable levels after 3 weeks. Immunohistochemistry and in situ hybridization analyses consistently demonstrated that approximately 90% of virally labeled cells were PV INs (i.e., PV-expressing cortical interneurons) located in the cortex. Conversely, on average, 75% of PV cINs expressed the viral reporter, with a maximum sensitivity of 93% (Figures 4A and 4B). This demonstrates that E2 can target all PV cINs without layer or subtype bias. Consistent with specificity for PV cINs, slice recordings from mice revealed that neurons expressing the viral reporter exhibited electrophysiological properties characteristic of fast-spiking PV cINs located in the primary somatosensory cortex (S1) and prefrontal cortex (PFC) (Figure 4C and Figures 8A and 8B).

[0278] Although the viral reporter was primarily confined to the brain cortex, some positive cells were observed in other brain regions closely corresponding to SCN1A-expressing regions. E2 maintained high specificity for PV-expressing neurons in the primary visual cortex (V1), cingulate cortex, subiculum, hippocampal CA1, and substantia nigra pars reticulata (Figure 8C). Notably, virtually no viral reporter expression was observed outside the brain, except for a few cells observed in the liver (as expected with systemic delivery of any AAV) and lung (where SCN1A is expressed at low levels) (Figure 8D). These results demonstrate that despite systemic delivery, E2-containing vectors can selectively target PV-expressing neurons in various brain regions, although there is minimal nonspecific expression outside the central nervous system.

[0279] Many experimental paradigms and clinical applications may require local rather than systemic injection. To be useful in these situations, viral expression must retain a high level of specificity for PV cINs. Stereotactic-guided injection typically results in a higher number of viral particles per cell compared to systemic delivery, which may contribute to nonspecific expression. To test whether increasing viral load alters specificity, we locally injected equal amounts of rAAV-E2-dTomato at various titers into the cortex of adult mice and assessed reporter expression within PV cINs 1 week later (Figure 4D). Results showed that reporter expression levels increased with increasing titers, without significant changes in specificity.

[0280] Despite the predominance of PV-expressing interneurons in the mature cortex, early postnatal targeting of these PV cINs has been hampered by the relatively late expression of parvalbumin (approximately postnatal day 15, i.e., P15) and the lack of other early markers for this population. The involvement of PV cINs in developmental disorders highlights the need to target and manipulate this cell population during cortical circuit formation. Complex genetic strategies offer only partial solutions to achieve this in mice (i.e., Lhx6-Cre, Sst-Flp, and Cre- and Flp-dependent reporters). However, these strategies do not provide a means to easily manipulate these neurons before the second postnatal week.

[0281] To test whether the E2 enhancer targets fast-spiking cINs before the onset of parvalbumin expression, we examined its activity at various postnatal stages. Toward this goal, we performed a series of stereotaxically guided injections of rAAV-E2-dTomato across the early postnatal period (Figure 4E). We assessed reporter selectivity during the development of parvalbumin expression at P15. This assessment revealed that selectivity for PV cINs was greater than 50% at P1 injection, increasing to 67% by P7 injection, and exceeding 80% after P10 injection. We further used this approach to label PV cINs before P15. To identify fast-spiking cINs in this context, we used Lhx6-Cre / intact transgenic mice expressing GFP in medial ganglionic eminence (MGE)-derived interneurons (both PV cINs and SST cINs). By costaining for SST, PV cINs could be identified as GFP-positive / SST-negative. Specificity was achieved for PV at P4-P7 and P7-P10 time courses of 72% and 78%, respectively. Thus, this approach provides a means to study such neurons during circuit maturation using a single viral injection.

[0282] Example 3 - Viral monitoring and manipulation of PV cortical interneurons in mice Having demonstrated the accuracy of E2 expression in PV cINs using different injection methods and across developmental stages as described in Example 2, we evaluated the utility of this vector to study connectivity (using a presynaptic reporter) and activity (using imaging with a genetically encoded calcium reporter). When we used E2 to drive a synaptophysin-tdTomato fusion gene (see, e.g., Madisen, L. et al., 2012, Nat Neurosci, 15(5):793-802), reporter expression was restricted to PV cINs presynaptically, with terminals located peri-somatically on pyramidal neurons (Figure 5A). When we used this vector to drive GCaMP6f expression (Chen, TW et al., Nature, 499: 295-300 (2013)), we demonstrated recruitment of PV cINs upon vibrissa stimulation (Figure 5B and Figure 9A). Together, these results demonstrate that E2 provides an effective tool for monitoring various aspects of PV cIN biology.

[0283] Further studies were carried out to examine whether E2 was sufficient to induce functional changes in activity using chemogenetic or optogenetic approaches. We used E2 to express the chemogenetic receptor PSAM4-5HT3-LC in adult animals (Magnus, CJ et al., 2019, Science, 364(6436)). We observed that PV cINs in brain slices collected from these animals could be induced to fire when exposed to the actuator varenicline and currents were clamped below threshold (Figure 5C). Similar results were observed using the chemogenetic receptor Gq-DREADD (Armbruster, BN et al., PNAS USA, 104:5163-5168 (2007) (Figure 9C). Finally, constant, high-frequency laser stimulation of PV cINs expressing the red-shifted opsin C1V1 in brain slices resulted in firing that was time-locked to the stimulus (Figures 5D and 5E and 9A and 9B). Since the engagement of these neurons was demonstrated to result in simultaneous local inhibition, we investigated the role of virally labeled PV cINs in the regulation of PV activity. Laser stimulation consistently disrupted pyramidal neuron activity in the vicinity of cINs. Notably, this effect was abolished by picrotoxin treatment (Figures 5D and 9B). Having demonstrated the efficacy of the above method ex vivo, we investigated whether optogenetic stimulation of PV cINs could alter excitatory networks in vivo. Three weeks after local injection of AAV-E2-C1V1 into the primary visual cortex of adult animals, single-unit recordings were performed within the infected area at baseline and during laser stimulation. The identity of recorded neurons was distinguished based on spike amplitude and maximum firing frequency. Laser stimulation reliably increased the firing frequency of inhibitory interneurons, whereas excitatory neuron firing was silenced (Figure 5E). Together, these results demonstrate that E2 functionally engages PV cINs and can induce network inhibition both ex vivo and in vivo using chemogenetic or optogenetic approaches.

[0284] Example 4 - Viral monitoring and manipulation of PV cortical interneurons in primates, including humans The sequence of the E2 enhancer is highly conserved across mammalian species, including humans, suggesting a conserved role in gene regulation. We conducted studies to determine whether E2 regulatory elements could be used to target PV cINs across mammalian species. Using systemic (marmosets) or local (rats and macaques) injections of E2-carrying viral vectors (E2 viruses), we demonstrated targeting of PV cINs with approximately 90% specificity (Figure 6A). It has been reported that human brain tissue obtained during surgical resection can be cultured for long periods (Eugene, E. et al., 2014, J. Neurosci. Methods, 235:234-244). Taking advantage of the resilience of the human brain to remain healthy ex vivo, we exposed freshly resected subiculum or medial temporal cortex to E2 viruses. Over a 2-week culture period, we observed the gradual emergence of fluorescently labeled cells. In regions where PV staining reflected the expected distribution of these cells, virally labeled cells were PV positive (Fig. 6B(i); see Methods for details). Furthermore, the majority of cells in both the cortex and subiculum exhibited distinctive features of PV INs as indicated by multiple criteria, including morphology, maximal firing frequency when evoked by direct depolarization, or optogenetic light stimulation (Fig. 6B(ii-iv) and Fig. 10A and 10B).

[0285] Notably, the human E2 enhancer showed similar specificity for PV cINs when injected into mice. This further demonstrates that noncoding regions of the genome, characterized by a high degree of sequence conservation, are likely to retain functional properties across species. Finally, truncation of both the 5' and 3' ends of the human E2 enhancer dramatically reduced specificity, suggesting that the functional boundaries of the E2 enhancer have been optimally identified (Figure 14). Together, these results demonstrate that E2 vectors are effective tools for targeting and manipulating PV cINs across mammalian species, including humans.

[0286] Example 5 - Identification of viral enhancers with region specificity To demonstrate the generalizability of the enhancer selection method described herein, 25 additional enhancer / regulatory element candidates (referred to herein as E11–E35) were identified near seven genes enriched in PV cINs across species (Figures 1A-1–1A-3; Figures 15A-1 and 15A-2; Figures 16A-1 and 16A-2) (see Methods below). Systemic injection of AAV containing these sequences revealed that four of them exhibited greater than 90% selectivity for PV cINs. Notably, among these enhancers, relatively few virus-labeled neurons that do not express PV were positive for the pan-interneuron marker Gad1. In Figures 1A-1–1A-3, Pvalb (UniProtKB-P20472) refers to the gene encoding the calcium-binding parvalbumin α protein. ACAN (NCBI Gene ID: 176; UniProt P16112) is a gene encoding aggrecan core protein (also known as cartilage-specific proteoglycan core protein), which may be involved in the disease spondyloepiphyseal dysplasia. Tmem132c (NCBI Gene ID: 92293) is a gene encoding transmembrane protein 132c, a type of protein that spans the biological membrane of cells or organelles. Lrrc38 (UniProtKB-Q5VT99) is a leucine-rich repeat-containing gene that shows relatively high expression in adrenal and prostate tissues. Inpp5j (UniProtKB-Q15735) is a gene encoding phosphatidylinositol 4,5-bisphosphate 5-phosphatase A, which may be involved in the functional regulation of inositol- and phosphatidylinositol phosphate-binding proteins in membrane ruffles. Mef2c (UniProtKB-Q06413) refers to the gene encoding myocyte-specific enhancer factor 2C, a transcription factor of the Mef2 family involved in cardiac morphogenesis, myogenesis, vascular development, and neurogenesis, as well as in the development of cortical structures.In humans, mutations in the Mef2c gene cause autosomal dominant mental retardation 20 (MRD20), characterized by severe psychomotor impairment, periodic tremor, and abnormal EEG and epilepsy. Pth1h (NCBI Gene ID: 5744) refers to the gene encoding a parathyroid hormone-like peptide secreted by cancer cells, such as breast, lung, ovarian, pancreatic, prostate, liver, or colorectal cancer cells, which causes humoral hypercalcmia of malignancy by activating type 1 PTH / PTHrP receptors in the kidney and bone. Like SCN1A, these genes are highly enriched in PV interneurons compared with all other cells in the brain. Therefore, we selected these genes as candidates for targeting with enhancer elements and identified and located described enhancers near the coding sequences of these genes.

[0287] In particular, four PV-specific regulatory elements, namely, E11 (SEQ ID NO:25, human), E14 (SEQ ID NO:28, human), E22 (SEQ ID NO:36, human), and E29 (SEQ ID NO:43, human), were identified as having highly selective expression within specific brain regions (Figures 13A and 13B). Each of these four enhancers is specific to distinct but overlapping subsets of PV-expressing neurons. Specifically, E11 and E14 showed a bias toward targeting PV cINs in the upper layers of the cortex, whereas the E22 enhancer showed expression almost exclusively restricted to the cortex, with only a few neurons showing low levels of expression elsewhere. In contrast, the E29 enhancer showed the most global expression, targeting the entire PV-expressing neuronal population throughout the central nervous system. All of these enhancers showed a high degree of sequence conservation and were selected from genes with similar expression profiles across species. To directly test whether cross-species similarity between enhancers leads to similar function across species, we locally injected AAV-E22-dTomato into V1 of macaques. We found that viral reporter expression was restricted to PV cINs in a manner similar to that observed in mice. The combination of regional selectivity and cross-species expression conservation provides utility for these viral agents in targeted therapies to correct abnormal brain function in different mammalian species.

[0288] Example 6 - Delivery of a functional SCN1A gene copy into the SCN1A-expressing population of a DS mouse model restores SCN1A expression to normal levels To restore SCN1A gene expression to normal levels by delivering functional SCN1A gene copies to SCN1A-expressing interneuron cell populations, such as those in DS mouse models, one or more approaches can be used to create rAAV vectors that can accommodate the size of the SCN1A gene, thereby increasing the "limited nucleic acid (DNA) payload" (i.e., the size of the exogenous nucleic acid (DNA), e.g., transgene and associated nucleic acid sequences, contained within or carried by the rAAV vector). As previously mentioned, while AAV DNA is approximately 4.7-5 kb, genes desired for insertion into and delivery by rAAV vectors are often twice or more that size. Delivery of larger genes using rAAV has been demonstrated in other situations using multiple vectors that reassemble by homologous recombination or acceptor site-mediated splicing (see, e.g., Hirsch, ML et al., 2016, Methods Mol Biol, 1382:21-39). Both of these approaches can be used to overcome the packaging limitations of rAAV.

[0289] As has been demonstrated in both DS animal models and human patients, the requirement for SCN1A is dose-dependent. Therefore, the expression level of SCN1A driven by rAAV is appropriately titrated as known and implemented in the art to match, or match as closely as possible, the normal endogenous SCN1A expression level. Several methods can be used to precisely regulate SCN1A gene expression levels. Various strategies are used to regulate SCN1A expression levels, using seizure remission as a direct measure of treatment effectiveness.

[0290] Example 7 - Pharmacogenetic approach to selectively normalize the excitability of SCN1A-deficient neuronal populations in a DS mouse model As an alternative to direct gene therapy using rAAV vectors carrying specific enhancer and gene nucleic acid sequences for delivery and restricted expression in interneuron cells, pharmacogenetic methods can be used to directly correct neuronal activity within the SCN1A neuron population. Toward this goal, a chemical genetic approach involving "designer receptors" can be used to modulate interneuron activity. Designer receptors exclusively activated by designer drugs (DREADDs) are engineered human muscarinic receptors. Furthermore, PSAM-PSEM chemical genetic agents are suitable for use.

[0291] Gq-DREADD receptors, receptors exclusively activated by the pharmacologically inactive and orally bioavailable drug clozapine-N4-oxide (CNO), may be used to correct excitatory / inhibitory balance (E / I balance) in DS mouse models (DS mice). Briefly, Gq-DREADD receptors are expressed in SCN1A-deficient interneuron cells using rAAV vectors carrying the SCN1A gene and an SCN1A-specific enhancer, e.g., E1-E10, as described above. Based on other studies with Gq-DREADDs, the receptors are expected to function and be located at the membrane of transduced / infected cells. Furthermore, rAAV vectors containing the SCN1a-specific regulatory elements, e.g., E1-E10, described herein should express Gq-DREADD receptors exclusively in interneurons, e.g., GABAergic interneurons and PV-expressing GABAergic interneurons. The function of Gq-DREADDs in infected cells can be assessed. Following CNO bath application, all Gq-DREADD-expressing interneurons are expected to exhibit membrane potential depolarization within less than one minute, consistent with functional receptor expression. Furthermore, following clozapine-N-oxide (CNO) application, voltage-clamp recordings of pyramidal cells near Gq-DREADD-expressing interneurons are expected to demonstrate an increase in inhibitory postsynaptic currents (IPSCs). These experiments demonstrate that rAAVs containing the SCN1a-specific E1-E10 enhancer sequence and a polynucleotide encoding Gq-DREADDs enable specific, functional, and restricted Gq-DREADD expression, and that CNO treatment effectively and selectively increases interneuron activity, thereby localizing and significantly increasing inhibitory activity by interneurons within neighboring excitatory neurons.

[0292] If the absence of SCN1A (SCN1A loss of function) impairs the ability of DREADDs to increase cellular excitability, then pan-interneuron enhancers, such as the separate and distinct Dlx enhancers described in Dimidschstein, J. et al. (2016, Nature Neuroscience, 19(12):1743-1749), can be used to deliver DREADDs to all interneurons, avoiding damage by increasing the activity of other types of interneurons that are not affected by SCN1A loss of function.

[0293] Example 8 - Materials and Methods for Previous Examples scATAC-seq library preparation and sequencing Male hemizygous Dlx6a-Cre mice (Jax stock #008199) were mated with female homozygous intact mice (flox-Sun1-eGFP, Jax stock #021039) to generate Dlx6a-Cre::intact offspring for scATAC-seq experiments. Brains from P28 Dlx6aCre::intact mice were harvested and coronal sections were prepared using a mouse brain slicer (Zivic Instruments). Regions of interest were dissected in ice-cold artificial cerebrospinal fluid (ACSF). The tissue was then transferred to a dounce homogenizer containing lysis buffer (10 mM Tris-HCl, 10 mM NaCl, 3 mM MgCl2, 0.01% Tween-20, and 0.01% IGEPAL CA-630, 0.001% digitonin). Tissues were homogenized using pestle A 10 times and pestle B 10 times, incubated on ice for 5 minutes, filtered through a 30 μm filter, and centrifuged at 500 x g for 10 minutes at 4°C. The pellet was resuspended in 1% BSA for sorting GFP+ nuclei using a Sony SH800S cell sorter. Nuclei were sorted and placed in Diluted Nuclei Buffer (10X Genomics). Single-cell ATAC-seq libraries were prepared using Chromium Single Cell ATAC Solution (10X Genomics). Libraries were sequenced using the Nova-Seq S2 100 cycle kit (Illumina) (Figures 3A-3C).

[0294] scATAC analysis Raw sequencing data were run through the Cell Ranger ATAC pipeline (10X Genomics). The fragment files were then used to generate snap files for analysis using the snapATAC package (https: / / doi.org / 10.1101 / 615179). Cells were clustered using graph-based clustering (k = 15, 24 principal components). Gene activity scores were generated as described in the snapATAC package and used to determine clusters corresponding to major interneuron classes. For each major class, bigwig files were generated and peaks were called using macs2 for input into the Integrated Genome Browser and enhancer selection. Peaks between major classes were compared using bedtools Jaccard.

[0295] Enhancer Selection All enhancers presented here (S5E1–E10 and E11–E35) were selected based on colocalization in ATACseq data (for DNA accessibility) and conservation across species (using the vertebrate conservation track in the UCSC Genome Browser). Genomic coordinates for mouse and their human orthologs are shown in Figures 1A-1–1A-3.

[0296] Candidate regulatory elements were manually curated from an element list created by intersecting the "context" region for selection (SCN1A intergenic region + intron 1) with the "ATAseq peak union" and "Phastcons 60-way" files—see below. Accessibility. ATAC-seq data (Mo et al., 2015, Neuron, 86:1369-1384) were downloaded from the GEO repository and discretized into peaks using MACS2 run with default parameters (https: / / github.com / taoliu / MACS). A custom R script was used to create a file containing the union of all peaks across the entire dataset, which was used for enhancer selection as described below. Final selection relied on examining peaks in individual cell types rather than the union of all peaks. Methylation. Mouse mCH levels in non-overlapping 100 kb bins spanning the entire mouse genome (Luo et al., 2018, Nat Commun, 9(1):3824) were downloaded from the Brainome portal (http: / / brainome.org). These data were used to support the positioning of candidates selected using the ATAC-seq dataset described above. Storage. The "phascons 60-way" track was downloaded in BED file format from the UCSC portal (https: / / genome.ucsc.edu), filtered to remove elements smaller than 10 bp, and filtered using a custom R script to fuse all elements separated by less than 50 bp using Bedtools / Interesct.

[0297] rAAV cloning and virus production All viral constructs were generated using standard molecular biology cloning methods and protocols. The plasmid pAAV-mDlx-GFP (Addgene #83900; Addgene, Watertown, MA) (Dimidschstein, J. et al., 2016, Nat. Neuroscience, 19(12):1743-1749) was used to create a standard backbone containing the elements required for AAV production (internal terminal repeats, minimal promoter, woodchuck posttranscriptional response element).

[0298] Enhancer sequences (necessary to restrict expression to specific types of neurons) were synthesized de novo by Genewiz (Cambridge, MA), and reporter and effector sequences were PCR amplified. In particular, the enhancer sequences were amplified using the following primers: E1: The enhancer, reporter, and effector genes were PCR amplified from mouse genomic DNA using TIFF2025118768000053.tif85151. Enhancers, reporters, and effectors were cloned using the Gibson Cloning Assembly Kit (NEB-E5510S) according to standard procedures. Specifically, for AAV-E1:10-dTomato, the dTomato coding sequence was amplified from the Addgene #83897 plasmid; for AAV-E2-SYP-dTomato, the synaptophysin-tdTomato coding sequence was amplified from the Addgene #34881 plasmid; for AAV-E2-GCaMP6f, the GCaMP6f coding sequence was amplified from the Addgene #83899 plasmid; and for AAV-E2-C1V1-eYFP, the C1V1-eYFP coding sequence was amplified from the Addgene #35499 plasmid.

[0299] The final plasmid was assembled using the Gibson Assembly® Cloning Kit (NEB-E5510S) (New England BioLabs, Ipswich, MA) according to the manufacturer's instructions and standard protocols. rAAV was produced using standard production methods. Polyethylenimine (PEI) was used for transfection (see, e.g., Longo, PA et al., 2013, Methods Enzymol., 529:227-240), and OptiPrep™ density gradients (Sigma-Aldrich, St. Louis, MO) were used for viral particle purification and isolation. Serotype 1 was used to produce AAV for local injection in mice and rats. Serotype 9 was used for systemic injection in marmosets, and serotype PHPeB was used for local injection in macaques and systemic injection in mice. Viral titers were assessed by qPCR and primer annealing via the WPRE sequence common to all constructs. All produced batches were 10 10 ~10 12 The viral genomes / ml ranged from 10 to 1500. In particular, the woodchuck hepatitis virus (WHP) posttranscriptional regulatory element (WPRE) is a DNA sequence that, when transcribed, creates a tertiary structure that enhances expression. WPRE, a tripartite regulatory element with γ, α, and β components, is commonly used in molecular biology to increase the expression of genes delivered by viral vectors, such as rAAV-dTomato. (See, e.g., Choi, J.-H. et al., 2014, Mol. Brain, 7:17.) All rAAV batches produced were 10 10 ~10 12 viral genomes / ml.

[0300] animal mouse: Female C57BL / 6J mice (Mus musculus; 10 weeks old) were obtained from Jackson Labs (Bar Harbor, ME - stock #000664). Rats: Sprague-Dawley rats (adult 150-250 gm) were obtained from Charles River labs, Kingston, NY. Marmosets: One female common marmoset (Callithrix jacchus; 6.0 years old) was obtained from the colony at the Massachusetts Institute of Technology. Macaques: One male macaque (Macaca mulatta; 15.0 years old) was obtained from the California National Primate Research Center at the University of California, Davis. All animals were maintained on a 12:12 light / 12:12 dark cycle with a maximum of five animals per cage for mice and one animal per cage for rats. Marmosets and macaques were socially housed. All animal care and experimental procedures were conducted in accordance with guidelines established by the Institutional Animal Care and Use Committees of the Broad Institute of MIT and Harvard (mice), the McGovern Research Institute at MIT (rats and marmosets), and the Salk Institute for Biological Studies (macaques), and adhere to National Institutes of Health standards.

[0301] Local and systemic viral injections Local S1 injections in adult mice were performed by stereotaxic injection into the somatosensory cortex at the following coordinates: 1.0 mm posterior, 2.9 mm lateral, and 0.7 / 0.45 mm ventral to bregma, using 150 nL of virus. Systemic injections in adult mice were performed using approximately 1000 μg of virus per animal. 11Virus particles were injected into the retro-orbital sinus. Post-operative monitoring was performed 5 days after injection. Local injection in rats in V1. Local injections in adult rats were performed using 670 nL of virus by stereotaxic guidance into the primary visual cortex at the following coordinates: 5.4 mm posterior, 4.2 mm lateral, and 2.0 mm ventral to bregma. Systemic injection in marmosets. For systemic injections in adult marmosets, approximately 10 virus particles dissolved in approximately 0.7 ml of sterile PBS were used. 12 After injection of 100 viral particles into the saphenous vein, approximately 0.5 ml of saline was injected once more. Pressure was applied to the injection site after the final injection to ensure hemostasis. The animals were returned to their home cages and closely monitored for normal post-anesthesia behavior. The animals were euthanized 51 days after virus injection. Local injection in macaques in V1. Local injections in adult macaques were performed via stereotactic guidance into the left primary visual cortex at the following coordinates: 13 mm posterior, 19 mm lateral, and 23 mm superior to the center of the interaural line (based on the animal's MRI). A total volume of 333 nL was injected at four depths (i.e., 1.8 mm, 1.3 mm, 0.8 mm, and 0.3 mm from the cortical surface).

[0302] surgery For stereotaxically guided virus injections, animals were anesthetized with isoflurane (1–3% in oxygen) and placed in a stereotaxic head frame on a temperature-controlled heating pad. A craniotomy and dura incision were made over the brain region of interest. Animals were injected with 50–500 nL of the indicated virus (rAAV) using a sharp glass pipette (25–35 mm diameter) at a rate of 10–25 nL / min and left in place for 5–15 min after injection to minimize reflux. The craniotomy site was covered with sterile bone wax, the surgical opening was closed with Vetbond, and the animals were returned to their home cage for at least 1 week. Injection sites were defined by the following coordinates: somatosensory cortex S1: 1.0 mm posterior, 3.0 mm lateral, 0.7 / 0.4 mm ventral to bregma; hippocampus CA1: 1.6 mm posterior, 1.8 mm lateral, 1.2 mm ventral to bregma; striatum: 0.5 mm posterior, 2.0 mm lateral, 3.2 mm ventral to bregma.

[0303] For retro-orbital vein injections, animals were anesthetized with isoflurane (1–3% in oxygen) and placed on a temperature-controlled heating pad. Intravenous (IV) injections were performed into the retro-orbital plexus. Specifically, mice were placed in a funnel-shaped nose cone connected to a non-rebreathing device (Surgivet, Dublin, OH), and the needle was inserted into the retro-orbital sinus, beveled at the medial canthus. Up to 150 μL of supernatant containing replication-defective rAAV vectors was injected into the tail vein or retro-orbital plexus. After injection, the eyes were kept closed for a minimum of 30 seconds to ensure homeostasis.

[0304] Electrophysiological recordings in mice: Slice preparation of 2- to 6-week-old mice. Virus-injected mice were anesthetized with isofluorane. Immediately after loss of reflexes, mice were transcardially perfused with ice-cold oxygenated ACSF containing the following (mM): 87 NaCl, 75 sucrose, 2.5 KCl, 1.25 NaH2PO4, 26 NaHCO3, 10 glucose, 1 CaCl2, and 2 MgCl2. Mice were then decapitated, and 300 μm-thick coronal slices were cut using a Leica VT-1200-S vibratome. The slices were placed in a holding chamber and incubated at 32-35°C for 15-30 min, followed by continued incubation at room temperature (20-23.5°C, 68-74°F) for at least 45-60 min before physiological recordings. The slice containing the injection site was transferred to a recording chamber immersed in oxygenated ACSF containing the following (mM): 125 NaCl, 2.5 KCl, 1.25 NaH2PO4, 26 NaHCO3, 10 glucose, 2 CaCl2, and 1 MgCl2 (pH = 7.4, bubbled with 95% O2 and 5% CO2). Slice preparation for mice 6 weeks of age or older. Acute coronal brain slices were prepared as follows. Mice were anesthetized with Avertin solution (20 mg / ml, 0.5 mg / g body weight) and transcardially perfused with 15–20 ml of ice-cold, carbogenated (95% O2, 5% CO2) cutting solution containing the following: 194 mM sucrose, 30 mM NaCl, 4.5 mM KCl, 1.2 mM NaH2PO4, 0.2 mM CaCl2, 2 mM MgCl2, 26 mM NaHCO3, and 10 mM D-(+)-glucose (osmolarity of 340–350 mOsm). The brain was then quickly removed and placed in ice-cold cutting solution for slice preparation. Coronal slices (300 μm) were prepared and then incubated with carbonated artificial cerebrospinal fluid (aCSF) at 32 °C for 10–15 min.Slices were then placed in CSF containing the following: 119 mM NaCl, 2.3 mM KCl, 1.0 mM NaH2PO4, 26 mM NaHCO3, 11 mM glucose, 1.3 mM MgSO4, and 2.5 mM CaCl2 (pH 7.4, osmolarity 295-305 mOsm) and incubated for at least 1 h at room temperature for current clamp. For interneuron recordings, 10 μM CNQX, 25 μM AP-5, and 10 μM SR-95531 were also added to stimulate AMPA, NMDA, and GABA, respectively. ACell-specific effects of optogenetic and chemogenetic stimulation were measured by adding receptor blocking agents. Whole-cell current-clamp recordings were obtained from visually identified viral reporter-expressing cells using borosilicate pipettes (3–5 MΩ) containing (mM) 130 K-gluconate, 6.3 KCl, 0.5 EGTA, 10 HEPES, 4 Mg-ATP, 0.3 Na-GTP, and 0.3% biocytin (pH adjusted to 7.3 with KOH). Immediately after break-in, series resistance (typically 15–25 MΩ) was compensated, and only stable recordings (<20% change) were included. Data were acquired using a MultiClamp 700B amplifier (Molecular Devices), sampled at 20 kHz, and filtered at 10 kHz. All cells were held at -60 mV with a DC current, and a current-step protocol was applied to obtain firing patterns and extract basic subthreshold and suprathreshold electrophysiological properties. Voltage clamp was performed. Cells not expressing the viral reporter were selected by pyramidal cell-shaped somata under IR-DIC visualization and recorded with a pipette containing (mM) 130 Cs-gluconate, 0.5 EGTA, 7 KCl, 10 HEPES, 4 Mg-ATP, 0.3 Na-GTP, 5 phosphocreatine, 5 QX-314, and 0.3% biocytin (pH adjusted to 7.3 with CsOH). Cells were continuously held at 0 mV for baseline and optogenetic or chemogenetic stimulation. For both current-clamp and voltage-clamp recordings, a baseline of at least 2 min was recorded before stimulation. To monitor changes in series resistance, small pulses (-20 pA or -5 mV, 100 ms at 0.2 Hz or 0.5 Hz) were applied throughout baseline and CNO application. Data were analyzed offline using Clampfit 10.2 software (Molecular Devices).

[0305] In vivo calcium imaging Approximately 100 nL of AAV-E2-GCaMP6 virus was injected into the barrel cortex of postnatal day 10 animals. Between P27 and P34, a craniotomy was implanted over the injection site, and wide-field calcium imaging was performed after recovery from the craniotomy. Anesthetized (1.5% isoflurane) mice were imaged at 3–4 Hz using 4x magnification (Thorlabs CCD camera-1501M-USB, Thorlabs LED stimulation-DC4104) during brief, timed intervals (5–20 s) of air puffs (100–200 ms duration, Picospritzer III) directed at the contralateral sinus hairs. Multiple recordings were made, and the mice were subsequently perfused for histological analysis. Recordings were analyzed in ImageJ by calculating F / F (change in fluorescence / mean fluorescence) for each recording and for simultaneous sinus hair stimulation. A threshold of (5%) F / F was set for both stimulated and spontaneous calcium signal responses.

[0306] Electrophysiological recordings in humans Tissue preparation, culture protocol, and viral inoculation. Four participants (two males and two females; ages 22–57 years) underwent surgical resection of brain tissue (temporal lobe and hippocampus) to treat drug-resistant epilepsy. In all cases, each participant had previously undergone primary surgery to place subdural and / or depth electrodes for intracranial monitoring to identify the location of seizure onset. The NINDS Institutional Review Board (IRB) approved the study protocol (ClinicalTrials.gov Identifier NCT01273129), and participants provided informed consent for the experimental use of the resected tissue. Within 30 minutes after neurosurgical resection, 300 μm slices were obtained from both the hippocampus and temporal lobe (Leica 1200S Vibratome; Leica Microsystems, Bannockburn, IL) and placed in ice-cold oxygenated sucrose-based cutting solution (100 mM sucrose, 80 mM NaCl, 3.5 mM KCl, 24 mM NaHCO3, 1.25 mM NaH2PO4, 4.5 mM MgCl2, 0.5 mM CaCl2, and 10 mM glucose, saturated with 95% O2 and 5% CO2). Slices were then incubated in the sucrose cutting solution at 33°C for 30 minutes and allowed to cool to room temperature for 15–30 minutes. Slices were then transferred to culture medium (Eugene et al., 2014) and placed in a 35°C incubator (5% CO2) for 15 minutes of equilibration. Each slice was then transferred to a 30 mm Millicell Cell Culture Insert (Millipore; Cat. No. PICM0RG50) for interface culture and incubated as described above. After 12 hours, the culture medium was replaced, and 1–2 μl of pAAV_S5E2-dTomato, with or without pAAV_S5E2_C1V1-eYFP, was pipetted directly onto each slice and returned to the incubator. For hippocampal slices, the virus was targeted to the subiculum. The culture medium was routinely replaced every 2–3 days until electrophysiological analysis. Electrophysiological recordings.Electrophysiological recordings were performed from cultured human slices 7–14 days after virus inoculation. Cultured human slices were transferred to a recording chamber perfused with extracellular solution (130 mM NaCl, 3.5 mM KCl, 24 mM NaHCO3, 1.25 mM NaH2PO4-H2O, 10 mM glucose, 2.5 mM CaCl2, and 1.5 mM MgCl2 (pH 7.4; 300–310 mOsm) saturated with 95% O2 / 5% CO2) at a rate of 3–4 ml / min at 33 °C. Whole-cell patch-clamp recordings from neurons infected with pAAV_S5E2-dTomato or pAAV_S5E2_C1V1-eYFP were performed using the following composition: 130 mM K-gluconate, 10 mM HEPES, 0.6 mM EGTA, 2 mM MgCl2, 2 mM Na2ATP, 0.3 mM ATP. Recordings were performed using an intracellular solution of 0.1% NaGTP and 0.5% biocytin (pH adjusted to 7.4; osmolarity adjusted to 285-300 mOsm). In some recordings, 130 mM K-gluconate was replaced with 90 mM K-gluconate / 40% KCl. Intrinsic membrane and firing properties were assayed essentially as previously described (Tricoire, L. et al., 2011, J. Neurosci., 31(30):10948-70). C1V1 optogenetic activation stimulated with 550 nm light was delivered to the slices through a 40X water-immersion objective using a CoolLED pE-4000 Illumination system (Andover, UK). Biocytin reconstruction and immunocytochemistry were performed. After electrophysiological recordings, slices were reconstituted with 0.1 M K-gluconate / 40% KCl. Slices were drop-fixed overnight in 4% paraformaldehyde in PB. They were washed in 0.1M PB (3x15 min) and permeabilized / blocked in 0.5% Triton X-100 / 10% goat serum in 0.1M PB for at least 2 hours at room temperature. For combined biocytin retrieval and immunocytochemistry, an initial incubation in primary antibodies (rabbit anti-PV, Abcam, Cat. No. ab11427; guinea pig anti-RFP, SYSY, Cat. No. 390005) at a 1:1000 dilution was performed (40 hours at 4°C).Slices were washed 4x30 min at room temperature in 0.1 M PB and incubated overnight at 4°C in secondary antibodies (1:1000 for goat anti-guinea pig Alex-flour 555, Thermofisher catalog no. A21435; 1:500 for goat anti-rabbit Alexa-flour 647, Thermofisher catalog no. A32733; and 1:1000 for streptavidin Alexa Fluor™ 488, Thermofisher S1123). After a final washing step (4x30 min), slices were mounted on microscope slides with Prolong Gold antifade (Thermofisher; catalog no. P36930) for subsequent confocal microscopy analysis.

[0307] Immunohistochemistry (IHC) Virus-injected animals were euthanized with Euthasol (Virbac, USA) and transcardially perfused with 4% paraformaldehyde (PFA). Brains were placed in 4% PFA overnight and then sectioned at 50-60 μm (specifically, 50 μm) using a Leica VTS1000 vibrosector. Free-floating brain sections were permeabilized with 0.1% Triton X-100 and phosphate-buffered saline (PBS) for 30 min, washed three times with PBS, and incubated in blocking buffer (5% normal donkey serum in PBS) for 30 min. Sections were then incubated overnight at 4°C with the indicated combinations of primary antibodies in blocking buffer: chicken anti-GFP (Abcam USA, ab13970) at 1:1,000; rabbit anti-DsRed (Clontech USA 632496) at 1:1,000; goat anti-PV (Swant USA, PVG-213) at 1:1,000; guinea pig anti-PV (Swant USA, GP-72) at 1:1,000; rabbit anti-SST (Peninsula USA, T-4103.0050) at 1:2,000; and mouse anti-synaptotagmin-2 (ZFIN USA, #ZDB-ATB-081002-25) at 1:250. Sections were then washed three times with PBS, incubated with 1:1000 Alexa Fluor-conjugated secondary antibody (Invitrogen, USA), counterstained with DAPI (Sigma, USA), and mounted on glass slides using Fluoromount-G (Sigma, USA). Images of brain regions were acquired using a Zeiss LSM800 confocal microscope or a Zeiss Axioimager A1 epifluorescence microscope. PV IHC staining within human brain tissue was highly variable. Therefore, evaluation of virus specificity was performed within regions of the cortex and subiculum, where staining density reflects the known distribution and density of these cells. Given the variability of human brain tissue, accurate quantification was not possible with this method.

[0308] In situ hybridization The in situ hybridization probes (Gad1; product number 400951, Pvalb; product number 421931, VIP; product number 415961) used in the studies described herein were designed by Advanced Cell Diagnostics (Newark, CA, USA). Reagents in the RNAscope® Multiplex Fluorescent Reagent Kit v2 (product number 323100), RNAscope® Probe Diluent (product number 300041), HYBEZ™ ovens (product numbers 321710 / 321720), humidity control trays (product number 310012), and HYBEZ Humidifying Paper (product number 310025) were also obtained from Advanced Cell Diagnostics. TSA Plus Fluorescein, TSA Plus Cyanine 3, and TSA Plus Cyanine 5 were obtained from PerkinElmer (#NEL741, #NEL744, and #NEL745). Brain tissue was processed as described in the immunohistochemistry section above. Brain sections were washed once with PBS, then three times with 0.1% Triton X-100 and PBS, mounted on Superfrost Plus glass slides (Fisher Scientific, 12-550-15), and baked in a HYBEZ oven at 60°C for 25 minutes. Slides were then immersed in 4% PFA for 30 minutes and then washed three times with H2O. RNAscope H2O2 was applied to each section for 5 minutes at room temperature. Slides were then washed three times with H2O, then immersed in pre-warmed 90°C H2O for 15 seconds, followed by pre-warmed 90°C RNAscope Target Retrieval for 15 minutes. After washing the slides three times with H2O, RNAscope Protease III was applied to each section, which was then incubated in a HYBEZ oven for 15 minutes at 40°C. The slides were washed three times with H2O and then placed in a HYBEZ oven and incubated with probe solution diluted 1:50 in probe diluent for 2 hours at 40°C.Next, sections were washed three times with RNAscope wash buffer before fluorescent amplification. Notably, the reporter RNA probe revealed nonspecific staining, likely due to viral DNA. To reveal the viral reporter, the RNAscope protocol was performed with IHC amplification of dTomato. Sections were incubated in blocking solution (0.3% Triton X-100 + 5% normal horse serum in PBS) for 30 minutes. Following this, sections were incubated overnight at 4°C in antibody solution (0.1% Triton X-100 + 5% normal horse serum in PBS) containing rabbit anti-DsRed (Clontech USA 632496) at 1:250. Sections were then washed three times with PBS, incubated with Alexa Fluor-conjugated secondary antibody (Invitrogen, USA) at 1:500, counterstained with DAPI (Sigma, USA), and mounted on glass slides using Fluoromount-...

Claims

1. A composition for use in targeting expression of an exogenous gene of interest to neuronal or interneuronal cells of a subject, comprising: the composition comprises a viral vector, or a virus particle or virus-like particle comprising said viral vector; The viral vector 1) a polynucleotide sequence of an exogenous gene of interest selected from the group consisting of a reporter gene, a designer receptor exclusively activated by designer drugs (DREADD)-encoding gene, a pharmacologically selective actuator molecule (PSAM)-encoding therapeutic gene, an effector gene, a therapeutic gene, or an SCN1A gene; 2) (i) the sequence of an isolated enhancer polynucleotide selected from the group consisting of isolated human enhancer element E1 having the sequence set forth in SEQ ID NO: 15, isolated human enhancer element E2 having the sequence set forth in SEQ ID NO: 16, isolated human enhancer element E3 having the sequence set forth in SEQ ID NO: 17, isolated human enhancer element E4 having the sequence set forth in SEQ ID NO: 18, isolated human enhancer element E5 having the sequence set forth in SEQ ID NO: 19, isolated human enhancer element E6 having the sequence set forth in SEQ ID NO: 20, isolated human enhancer element E7 having the sequence set forth in SEQ ID NO: 21, isolated human enhancer element E8 having the sequence set forth in SEQ ID NO: 22, isolated human enhancer element E9 having the sequence set forth in SEQ ID NO: 23, and isolated human enhancer element E10 having the sequence set forth in SEQ ID NO: 24; or (ii) the sequence of an isolated enhancer polynucleotide selected from the group consisting of an isolated mouse enhancer element E1 having the sequence set forth in SEQ ID NO: 5, an isolated mouse enhancer element E2 having the sequence set forth in SEQ ID NO: 6, an isolated mouse enhancer element E3 having the sequence set forth in SEQ ID NO: 7, an isolated mouse enhancer element E4 having the sequence set forth in SEQ ID NO: 8, an isolated mouse enhancer element E5 having the sequence set forth in SEQ ID NO: 9, an isolated mouse enhancer element E6 having the sequence set forth in SEQ ID NO: 10, an isolated mouse enhancer element E7 having the sequence set forth in SEQ ID NO: 11, an isolated mouse enhancer element E8 having the sequence set forth in SEQ ID NO: 12, an isolated mouse enhancer element E9 having the sequence set forth in SEQ ID NO: 13, and an isolated mouse enhancer element E10 having the sequence set forth in SEQ ID NO:

14. and The isolated enhancer polynucleotide specifically restricts expression of an exogenous gene of interest to brain parvalbumin (PV)-expressing cortical interneuron cells, brain vasoactive intestinal peptide-expressing cortical interneuron cells (VIP cIN), and brain pyramidal (PYR) neurons. The composition.

2. The isolated enhancer polynucleotide is a human enhancer element E2 having the sequence set forth in SEQ ID NO: 16; or the isolated enhancer polynucleotide is a human enhancer element E6 having the sequence set forth in SEQ ID NO: 20; or The isolated enhancer polynucleotide is a human enhancer element E5 having the sequence set forth in SEQ ID NO:

19. The composition of claim 1.

3. The isolated enhancer polynucleotide is a human enhancer element E2 having the sequence set forth in SEQ ID NO: 16, and specifically restricts expression of an exogenous gene of interest to parvalbumin (PV)-expressing cortical interneuron cells of the brain; or the isolated enhancer polynucleotide is a mouse enhancer element E2 having the sequence set forth in SEQ ID NO: 6, which specifically restricts expression of an exogenous gene of interest to parvalbumin (PV)-expressing cortical interneuron cells of the brain; or the isolated enhancer polynucleotide is a human enhancer element E6 having the sequence set forth in SEQ ID NO: 20, which specifically restricts expression of an exogenous gene of interest to vasoactive intestinal peptide-expressing cortical interneuron cells (VIP cINs) in the brain; or The isolated enhancer polynucleotide is a human enhancer element E5 having the sequence set forth in SEQ ID NO: 19, which specifically restricts expression of an exogenous gene of interest to pyramidal (PYR) neurons of the brain. The composition of claim 1.

4. The composition of claim 3, wherein the exogenous gene of interest is the SCN1A gene.

5. A composition described in any one of claims 1 to 4, wherein the exogenous gene of interest is a DREADD-encoding gene, and the DREADD-encoding gene is a Gq-DREADD-encoding gene that is activated by the chemogen clozapine-N4-oxide (CNO).

6. A composition described in any one of claims 1 to 5, wherein the viral vector is a recombinant adeno-associated virus (rAAV) vector.

7. The composition of any one of claims 1 to 6, wherein the interneuron cell is a GABAergic interneuron cell.

8. Interneuron cells are GABAergic interneuron cells located in the telencephalon of the brain; GABAergic interneuron cells express parvalbumin (PV) or vasoactive intestinal peptide (VIP); or The neuronal cells are pyramidal (PYR) neurons of the cerebral cortex, The composition of claim 7.

9. A composition described in any one of claims 1 to 8, wherein the neuronal cells or interneuronal cells are in a human subject.

10. A composition described in any one of claims 1 to 9, wherein the subject has a disease, disorder, or condition selected from one or more of epilepsy, seizures, or Dravet syndrome (DS).

11. The composition of any one of claims 1 to 10, further comprising a pharmaceutically acceptable vehicle, carrier, or diluent.

12. A composition described in any one of claims 1 to 11, for systemic, parenteral, intravenous, or intracerebral administration.

13. A composition described in any one of claims 1 to 12 formulated for administration as a prophylactic and / or in conjunction with adjunctive antiepileptic treatment.

14. A composition for use in limiting SCN1A expression and / or restoring normal levels of SCN1A expression in a GABAergic interneuron or neuronal cell in a subject having a deficient or defective level of SCN1A expression, comprising: the composition comprises a viral vector, or a virus particle or virus-like particle comprising said viral vector; The viral vector 1) Polynucleotide sequence of the SCN1A gene and 2) an isolated enhancer polynucleotide sequence selected from the group consisting of E1 having the sequence set forth in SEQ ID NO: 15, E2 having the sequence set forth in SEQ ID NO: 16, E3 having the sequence set forth in SEQ ID NO: 17, E4 having the sequence set forth in SEQ ID NO: 18, E5 having the sequence set forth in SEQ ID NO: 19, E6 having the sequence set forth in SEQ ID NO: 20, E7 having the sequence set forth in SEQ ID NO: 21, E8 having the sequence set forth in SEQ ID NO: 22, E9 having the sequence set forth in SEQ ID NO: 23, and E10 having the sequence set forth in SEQ ID NO: 24; Including, contacting a subject's GABAergic interneuronal or neuronal cells with an effective amount of a viral vector, viral particle, or virus-like particle, thereby restoring normal levels of SCN1A expression in the cells; The composition.

15. The composition described in claim 14, wherein SCN1A expression is restored in brain parvalbumin (PV)-expressing cortical interneuron cells, brain vasoactive intestinal peptide-expressing cortical interneuron cells (VIP cIN), or brain pyramidal (PYR) neurons.

16. A composition for use in treating a disease, disorder, or condition in a subject selected from one or more of epilepsy, seizures, or Dravet syndrome (DS), comprising: the composition comprises a viral vector, or a virus particle or virus-like particle comprising said viral vector; The viral vector 1) Polynucleotide sequence of the SCN1A gene and 2) an isolated enhancer polynucleotide sequence selected from the group consisting of E1 having the sequence set forth in SEQ ID NO: 15, E2 having the sequence set forth in SEQ ID NO: 16, E3 having the sequence set forth in SEQ ID NO: 17, E4 having the sequence set forth in SEQ ID NO: 18, E5 having the sequence set forth in SEQ ID NO: 19, E6 having the sequence set forth in SEQ ID NO: 20, E7 having the sequence set forth in SEQ ID NO: 21, E8 having the sequence set forth in SEQ ID NO: 22, E9 having the sequence set forth in SEQ ID NO: 23, and E10 having the sequence set forth in SEQ ID NO: 24; Including, The composition.

17. A composition described in any one of claims 14 to 16, wherein the isolated enhancer polynucleotide is a human enhancer element E2 having the sequence set forth in SEQ ID NO: 16, a human enhancer element E5 having the sequence set forth in SEQ ID NO: 19, or a human enhancer element E6 having the sequence set forth in SEQ ID NO:

20.

18. A composition described in any one of claims 14 to 17, wherein the viral vector comprises a recombinant adeno-associated virus (rAAV) vector.

19. A composition described in any one of claims 14 to 18, for systemic, parenteral, intravenous, or intracerebral administration.

20. A composition described in any one of claims 14 to 19, formulated for administration as a prophylactic and / or in conjunction with adjunctive anti-epileptic treatment.

21. A viral vector, or a viral particle or virus-like particle containing said viral vector, The viral vector comprises an enhancer polynucleotide sequence selected from SEQ ID NOs: 5 to 14 and specifically targets SCN1A-expressing neuronal cells, wherein the neuronal cells are parvalbumin cortical interneurons (PV cINs), pyramidal (PYR) neurons, or vasoactive intestinal peptide cortical interneurons (VIP cINs). The viral vector, virus particle, or virus-like particle.

22. 22. The viral vector, viral particle, or virus-like particle of claim 21, wherein the target cell is a PV-expressing neuronal cell.

23. A viral vector, viral particle, or virus-like particle as described in claim 21 or 22, wherein the enhancer polynucleotide comprises the sequence set forth in SEQ ID NO:

6.

24. A cell comprising the viral vector, virus particle, or virus-like particle of any one of claims 21 to 23.

25. A pharmaceutical composition comprising the viral vector, virus particle, or virus-like particle of any one of claims 21 to 23 and a pharmaceutically acceptable vehicle, carrier, or diluent.

26. A composition comprising: (i) a viral vector or a recombinant adeno-associated virus (rAAV) vector; or (ii) a viral particle or virus-like particle comprising said viral vector, The viral vector 1) a polynucleotide sequence of an exogenous gene of interest selected from the group consisting of a reporter gene, a designer receptor exclusively activated by designer drugs (DREADD)-encoding gene, a pharmacologically selective actuator molecule (PSAM)-encoding therapeutic gene, an effector gene, a therapeutic gene, or an SCN1A gene; 2) (i) the sequence of an isolated enhancer polynucleotide selected from the group consisting of isolated human enhancer element E1 having the sequence set forth in SEQ ID NO: 15, isolated human enhancer element E2 having the sequence set forth in SEQ ID NO: 16, isolated human enhancer element E3 having the sequence set forth in SEQ ID NO: 17, isolated human enhancer element E4 having the sequence set forth in SEQ ID NO: 18, isolated human enhancer element E5 having the sequence set forth in SEQ ID NO: 19, isolated human enhancer element E6 having the sequence set forth in SEQ ID NO: 20, isolated human enhancer element E7 having the sequence set forth in SEQ ID NO: 21, isolated human enhancer element E8 having the sequence set forth in SEQ ID NO: 22, isolated human enhancer element E9 having the sequence set forth in SEQ ID NO: 23, and isolated human enhancer element E10 having the sequence set forth in SEQ ID NO: 24; or (ii) the sequence of an isolated enhancer polynucleotide selected from the group consisting of an isolated mouse enhancer element E1 having the sequence set forth in SEQ ID NO: 5, an isolated mouse enhancer element E2 having the sequence set forth in SEQ ID NO: 6, an isolated mouse enhancer element E3 having the sequence set forth in SEQ ID NO: 7, an isolated mouse enhancer element E4 having the sequence set forth in SEQ ID NO: 8, an isolated mouse enhancer element E5 having the sequence set forth in SEQ ID NO: 9, an isolated mouse enhancer element E6 having the sequence set forth in SEQ ID NO: 10, an isolated mouse enhancer element E7 having the sequence set forth in SEQ ID NO: 11, an isolated mouse enhancer element E8 having the sequence set forth in SEQ ID NO: 12, an isolated mouse enhancer element E9 having the sequence set forth in SEQ ID NO: 13, and an isolated mouse enhancer element E10 having the sequence set forth in SEQ ID NO:

14. and The isolated enhancer polynucleotide specifically restricts expression of an exogenous gene of interest to brain parvalbumin (PV)-expressing cortical interneuron cells, brain vasoactive intestinal peptide-expressing cortical interneuron cells (VIP cIN), and brain pyramidal (PYR) neurons. The composition.

27. The composition of claim 26, wherein the viral vector comprises an isolated enhancer element polynucleotide having the sequence set forth in SEQ ID NO:

16.

28. The composition of claim 26, wherein the viral vector comprises an isolated enhancer element polynucleotide having the sequence set forth in SEQ ID NO:

6.

29. A composition described in claim 27 or 28, wherein the isolated enhancer element polynucleotide restricts expression of an exogenous gene of interest to parvalbumin (PV)-expressing cortical interneuron cells in the brain.

30. A cell comprising (i) a viral vector or a recombinant adeno-associated virus (rAAV) vector, or (ii) a virus particle or virus-like particle containing the viral vector, as defined in claim 26.

31. The composition of any one of claims 26 to 28, further comprising a pharmaceutically acceptable vehicle, carrier, or diluent.

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