Genetic constructs for silencing alpha-synuclein and uses thereof

Abstract

The present invention relates to nucleic acids, compositions and medical uses of said compositions in the treatment and / or prevention of Parkinson's disease (PD), multiple system atrophy (MSA) and / or other alpha-synucleopathies.

Description

[Technical field]

[0001] The present invention relates to nucleic acids, uses of said nucleic acids for reducing and / or knocking down the transcript of the alpha-synuclein (alpha-syn) gene (SNCA) and treating and / or preventing Parkinson's disease (PD) and other alpha-synucleopathies, particularly in the context of gene therapy. [Background technology]

[0002] Fibrillar α-synuclein inclusions define two major neurodegenerative disease classes: Lewy body diseases, e.g., PD, Lewy body dementia (LBD), including PD with dementia (PDD), and dementia with Lewy bodies (DLB), including multiple system atrophy (MSA), characterized by Papp-Lantos bodies, collectively referred to as synucleinopathies.

[0003] Parkinson's disease (PD) is a complex progressive neurodegenerative disorder that can cause motor and non-motor symptoms. Typical clinical features of PD include bradykinesia, resting tremor, rigidity, and / or postural instability that occurs in later stages. Non-motor symptoms can occur before and / or after clinical diagnosis. These include depression, sleep disturbances, pain and fatigue in early stages of the disease, and anxiety, dementia and cognitive impairment in later stages of the disease. Both motor and non-motor symptoms are debilitating for patients and burdensome for caregivers.

[0004] PD is a complex disease, the cause of which remains unknown, although a number of genes have been implicated in the etiology and / or development of PD. The main feature of PD pathology is the neurodegeneration of dopaminergic neurons in the substantia nigra, a midbrain brain region with associated dopaminergic projections to the striatum and cortex, which are central to movement-related functions. In addition to the loss of nigrostriatal dopaminergic innervation and degeneration in other brain regions, PD is characterized by the presence of cytoplasmic protein aggregates (Lewy bodies) that contain insoluble α-syn protein.

[0005] Native α-syn protein in the brain has no defined tertiary structure and is largely unfolded. Upon interaction with negatively charged lipids, such as the phospholipids that compose cell membranes, α-syn folds into an α-helical structure via its N-terminus. However, in PD, α-syn adopts an amyloid-like structure rich in β-sheets that is prone to aggregation. The aggregates constitute the majority of Lewy bodies.

[0006] MSA is a progressive adult-onset neurodegenerative disorder of undetermined etiology characterized by characteristic oligodendrogliosis with argyrophilic glial cytoplasmic inclusions (GCIs) and selective neurodegeneration. GCIs or Papp-Lantos inclusions / bodies are now accepted as the definitive neuropathological diagnostic feature of MSA and have been suggested to play a central role in the pathogenesis of the disorder. GCIs are composed of hyperphosphorylated α-syn, ubiquitin, LRRK2 (leucine-rich repeat serine / threonine protein) and other proteins.

[0007] Generally speaking, α-syn protein has a tendency to form aggregates, and these aggregates may lead to loss of normal function and / or toxic effects in neurons, resulting in neurodegeneration and / or neuroinflammation in different brain regions. Moreover, mutations or duplications / triplications of the α-syn gene are known to be associated with α-synucleopathies.

[0008] Currently, therapeutic approaches to treat and / or prevent diseases are based on completely knocking down genes and / or gene transcripts. However, due to the important physiological role of α-syn, depletion of α-syn protein may pose patient safety concerns due to phenomena such as attenuation of synaptic transmission in the central nervous system (CNS).

[0009] Thus, there remains a need to have therapies that can treat and / or prevent PD and / or other synucleinopathies while reducing and / or preventing undesirable safety risks. Summary of the Invention [Means for solving the problem]

[0010] A first aspect of the present invention relates to a nucleic acid ("nucleic acid of the present invention") comprising a nucleic acid sequence encoding an RNA ("RNA of the present invention"), wherein the RNA sequence comprised in said RNA is substantially complementary to a target sequence of the alpha-synuclein (alpha-syn) gene (SNCA), said RNA sequence has at least 15 nucleotides, and said RNA comprises a hairpin.

[0011] A second aspect of the invention relates to a nucleic acid of the invention which is a DNA molecule ("a DNA molecule of the invention").

[0012] A third aspect of the present invention relates to an adeno-associated virus (AAV) vehicle comprising the DNA molecule (the "AAV (vehicle) of the present invention").

[0013] Further aspects of the present invention relate to compositions comprising an AAV vehicle of the present invention and at least one pharma- ceutically acceptable excipient; methods for producing an AAV vehicle of the present invention; and kits comprising the AAV vehicle, in the case of the present invention, which further comprise an immunosuppressant compound. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0014] The present invention relates to gene therapy, and in particular to the use of RNA interference (RNAi) in gene therapy to target RNA encoded by the alpha-syn gene, preferably the human alpha-syn gene.

[0015] nucleic acid In accordance with the present invention, there is provided a nucleic acid ("nucleic acid of the present invention") comprising a nucleic acid sequence encoding an RNA ("RNA of the present invention"), wherein the RNA sequence comprised in the RNA is substantially complementary to a target sequence of an alpha-syn gene, the RNA sequence has at least 15 nucleotides, and the RNA comprises a hairpin.

[0016] The term "substantially complementary" as used herein refers to two nucleic acid sequences that are complementary to each other, whereby the two nucleic acid sequences bind to each other. The term "substantially" means that the complementarity between the two sequences is sufficient to bind to each other for a sufficient time to have at least a partial inhibitory effect. Of course, it is preferred that the complementarity is perfect (perfect complementarity), but some gaps and / or mismatches can be tolerated. The number of mismatches should be 10% or less. The important feature is that the complementarity is sufficient to allow binding of the two strands in situ. The binding should be strong enough to exert an inhibitory effect.

[0017] The nucleic acid sequence encoding said RNA may optionally have up to 4, 5, or 6 nucleotides that differ from the complementary ("anti") sequence of said target sequence. The nucleic acid sequence encoding an RNA may have 1, 2, or 3 nucleotides that differ from the complementary sequence of said target sequence encoded by the alpha-syn gene. Preferably, said nucleic acid sequence as described above is identical to the complementary sequence of said target sequence.

[0018] The term "alpha-syn gene" as used herein refers to the alpha-synuclein gene or the SNCA gene. The alpha-syn gene is preferably a mammalian alpha-syn gene, more preferably a mouse or rat alpha-syn gene, more preferably a NHP alpha-syn gene, and most preferably a human alpha-syn gene, as described herein. All SNPs of the alpha-syn gene may further be included in the present invention.

[0019] As used herein, the term "alpha-syn protein" refers to the protein encoded by the alpha-syn gene.

[0020] Typically, the nucleic acid according to the present invention is intended to reduce the expression of a disease-related gene. According to the present invention, said nucleic acid as described above can be delivered to a target cell, for example, by a gene delivery vehicle, in particular a viral gene delivery vehicle, preferably an adeno-associated virus (AAV) vehicle, as described below. The nucleic acid can then be transcribed into RNA. During RNA intervention (RNAi), the RNA is cleaved by Drosha (i.e., a class 2 ribonuclease III enzyme) in the nucleus of the target cell into short hairpin RNA (shRNA) or long hairpin RNA (lhRNA) without flanking regions at the 5' and 3' ends of the RNA. The cleaved RNA is then transported to the cytoplasm of the cell, where the cleaved RNA is not further cleaved by the endoribonuclease Dicer. The cleaved RNA is further cleaved by Argonaute-2 (AGO-2) of the RNA-induced silencing complex (RISC), and the passenger RNA sequence of the cleaved RNA is trimmed (i.e., cleaved) by poly(A)-specific ribonuclease (PARN). The other strand of the cleaved RNA is called the guide strand (i.e., the guide sequence). As described above, the guide strand that contains a sequence substantially complementary to the target RNA sequence is not processed and / or cleaved by AGO-2.

[0021] In the situation where the passenger strand of the cleaved RNA continues to exist without being excised, the passenger strand may be partially complementary to off-target sequences and / or even to the target sequence. Thus, the passenger strand can bind to the off-target sequence and / or even compete with the guide strand of the cleaved RNA to bind to the target sequence. Such "off-target problems" may affect the accuracy of gene editing interventions and therefore must be reduced and / or eliminated.

[0022] Thereby, the "off-target problem" can be prevented and / or suppressed by cleaving the passenger sequence, thus improving the binding specificity of the guide sequence to the target mRNA and reducing "off-target" events. This is a preferred embodiment of the present invention.

[0023] The present invention includes RNA that contains two complementary strands, one of which (passenger strand) is cleaved in RNAi. For example, double-stranded RNA (dsRNA), small interfering RNA (siRNA) and microRNA (miRNA) are included in the present invention.

[0024] The term "RNA hairpin" or "hairpin" as used herein refers to an RNA secondary structure that includes two complementary strands and a loop connecting the two strands. One strand is called the passenger strand (i.e., passenger sequence) and the other strand is called the guide strand (i.e., guide sequence). RNA hairpins can guide RNA folding, determine interactions in ribozymes, protect messenger RNA (mRNA) from degradation, and function as recognition motifs for RNA-binding proteins.

[0025] Other RNAs having two strands are also included in the present invention, provided that preferably one strand is degraded (i.e., trimmed) in RNA interference (RNAi) and the other strand remains undegraded, thereby improving the "off-target problem". lhRNA and / or shRNA can be included in the present invention. In certain embodiments, the hairpin can be shRNA or lhRNA.

[0026] Preferably, the hairpin as described above has a sequence of at least 39 nucleotides; at least 44 nucleotides; at least 49 nucleotides; at least 54 nucleotides; or at least 59 nucleotides. In some embodiments of the invention, the hairpin as described above has a sequence of at least 39 nucleotides. Thus, preferably, the nucleic acid sequence encoding the RNA has a sequence of at least 39 nucleotides.

[0027] Optionally, said hairpin as above has an RNA sequence of up to 80 nucleotides, optionally up to 78 nucleotides, optionally up to 76 nucleotides, optionally up to 74 nucleotides, optionally up to 72 nucleotides, optionally up to 70 nucleotides, optionally up to 68 nucleotides, optionally up to 66 nucleotides, and even optionally up to 64 nucleotides. Preferably, said hairpin as above has an RNA sequence of 72 nucleotides.

[0028] miRNA scaffolds The nucleic acid sequence encoding the hairpin having the above sequence length can be easily incorporated into AAV and delivered to target organs such as the central nervous system. Furthermore, the sequence length allows the hairpin to fold correctly, so that the passenger strand can be cleaved by RNAi as described above. Therefore, as described above, the sequence having the above sequence length can reduce and / or prevent the off-target problem. Furthermore, the off-target problem is further reduced and / or prevented by RNA having a sequence selected from the group consisting of SEQ ID NO:1, SEQ ID NO:2, and variants of SEQ ID NO:1 and SEQ ID NO:2.

[0029] Thus, in a preferred embodiment, said RNA (RNA of the invention) comprises SEQ ID NO:1, SEQ ID NO:2, or a variant of SEQ ID NO:1 or SEQ ID NO:2.

[0030] Thus, in a preferred embodiment, the present invention provides a nucleic acid comprising a nucleic acid sequence encoding an RNA, wherein the RNA sequence comprised in the RNA is substantially complementary to a target sequence of an alpha-syn gene, the RNA sequence has at least 15 nucleotides, the RNA comprises a hairpin, and the RNA comprises SEQ ID NO:1, SEQ ID NO:2, or a variant of SEQ ID NO:1 or SEQ ID NO:2.

[0031] SEQ ID NO: 1 refers to a miR451 scaffold or hairpin. The scaffold preferably comprises, from 5' to 3', first (i) 5'-CUUGGGAAUGGCAAGG-3' (SEQ ID NO: 46), followed by (ii) a 22 nucleotide sequence comprising or consisting of a first RNA sequence, followed by (iii) a 17 nucleotide sequence that can be considered a second RNA sequence complementary over its entire length to nucleotides 2 to 18 of said 22 nucleotide first sequence, followed by (iv) the sequence 5'-MWCUUGCUAUACCCAGA-3' (wherein M is G or C and W is A or U) (SEQ ID NO: 47). Preferably, the first 5'-A / C nucleotide of the latter sequence does not base pair with the first nucleotide of the first strand of the first or second RNA.

[0032] Such scaffolds may contain flanking sequences as found in the original pri-miR451 scaffold. Alternatively, the flanking sequences may be replaced by flanking sequences of other pri-mRNA structures. Exemplary scaffold pri-mRNA sequences of the present invention are shown in Table 3.

[0033] The miR451 scaffold allows induction of RNA interference (RNAi); in particular, RNAi is induced by the guide strand of this scaffold. The pri-miR451 scaffold does not provide passenger strands because its processing is different from the canonical miRNA processing pathway (Cheloufi, S. et.al., 2010 and Yang, J. Set. al., 2010). Thereby, the use of miR-451 can prevent or reduce the possibility of having undesirable potential off-targeting by passenger strands.

[0034] SEQ ID NO:2 refers to the miR-144 scaffold combined with the miR451 scaffold described above.

[0035] The nucleic acid may be transcribed into the RNA as described above. Preferably, the RNA comprises a hairpin of miR-451 comprising SEQ ID NO: 1. The use of the miR451 prevents and / or reduces the off-target problems described above, since the passenger strand is cleaved and not present in the final miR451. More preferably, the RNA comprises SEQ ID NO: 2 and has a double hairpin structure. The structure comprises, from the 5' to 3' end of the RNA, a hairpin miR144 followed by the hairpin miR451. It has been found that when the RNA comprises SEQ ID NO: 2, the off-target problems are prevented and / or reduced. Furthermore, the biogenesis of the hairpin miR451 is improved, thereby increasing the amount of the guide strand. Thus, the inhibition and / or knock-off of the transcription of the target RNA can be enhanced.

[0036] RNA variants of SEQ ID NO:1 or SEQ ID NO:2 are defined as having substantially the same function as RNA comprising SEQ ID NO:1 or SEQ ID NO:2, respectively. RNA comprising said variants of SEQ ID NO:1 or SEQ ID NO:2 has the function of preventing and / or reducing said off-target problems as described above. Said variants of SEQ ID NO:1 and SEQ ID NO:2 also have substantially the same function as SEQ ID NO:1 and SEQ ID NO:2, respectively, due to folding into RNA secondary structures. Furthermore, RNA comprising said variants of SEQ ID NO:2 can not only reduce and / or prevent said off-target problems as described above, but also improve the biogenesis of the hairpin.

[0037] As described herein, when the "off-target problem" is described as being reduced / ameliorated, it is meant that the off-target problem is prevented, reduced, and / or stopped.

[0038] Optionally, the variant of SEQ ID NO:1 above is substantially the same as SEQ ID NO:1 and has substantially the same function as SEQ ID NO:1 above. Optionally, the variant comprises at least one nucleotide, or optionally up to 5 nucleotides, that differ from SEQ ID NO:1. Optionally, the variant of SEQ ID NO:1 comprises up to 30 nucleotides; up to 25 nucleotides; up to 20 nucleotides; up to 15 nucleotides; or up to 10 nucleotides that differ from SEQ ID NO:1.

[0039] Optionally, the variant of SEQ ID NO:2 above is substantially the same as SEQ ID NO:2 and has substantially the same function as SEQ ID NO:2 above. Optionally, the variant may include at least one nucleotide that differs from SEQ ID NO:2, or optionally up to 5 nucleotides. Optionally, the variant of SEQ ID NO:2 includes up to 30 nucleotides; up to 25 nucleotides; up to 20 nucleotides; up to 15 nucleotides; or up to 10 nucleotides that differ from SEQ ID NO:2.

[0040] Preferably, the RNA sequence substantially complementary to the target RNA sequence encoded by the alpha-syn gene has at least 15 nucleotides, at least 16 nucleotides, at least 17 nucleotides, at least 18 nucleotides, at least 19 nucleotides, at least 20 nucleotides, at least 21 nucleotides, at least 22 nucleotides, at least 23 nucleotides, or at least 24 nucleotides. Preferably, the RNA sequences described herein have at least 18 nucleotides.

[0041] Optionally, the RNA sequence has at most 32 nucleotides, at most 31 nucleotides, at most 30 nucleotides, at most 29 nucleotides, at most 28 nucleotides, at most 27 nucleotides, at most 26 nucleotides, or at most 25 nucleotides. In some embodiments of the invention, the RNA sequence has at most 32 nucleotides. Thus, the nucleic acid sequence encoding the RNA has at most 32 nucleotides.

[0042] The RNA sequence having the above-mentioned sequence length constitutes the guide strand of the hairpin as described above. As described above, the length of the guide strand is designed to form the guide strand of the hairpin and allow the formation of an RNA secondary structure (i.e., hairpin). In addition, the length of the guide strand is selected to provide sufficient binding specificity to the target RNA. These contribute to reducing the off-target problem.

[0043] An RNA sequence substantially complementary to a target sequence of the alpha-syn gene (the sequence contained in the DNA) is designed based on one of the conserved regions of the alpha-syn gene, as described below.

[0044] Preferably, said conserved region is present in a mammalian alpha-syn gene, more preferably in a non-human primate (NHP) and / or human alpha-syn gene.

[0045] Preferably, the target RNA is encoded by a portion of an exon contained in the alpha-syn gene, which is useful to take into account when designing the target RNA, since exons are not removed by RNA splicing.

[0046] The term "(a) portion" as defined herein refers to a partial sequence. The term "exon" as defined herein refers to a region contained in the α-syn gene that encodes a portion of the mRNA without being removed by RNA splicing. An exon can include at least one conserved sequence. Exons contained in NHP and human α-syn genes were aligned to design the target RNA and the guide strand. For example, the NHP α-syn gene consists of the NHP α-syn gene (gene ID: 706985, https: / / www.ncbi.nlm.nih.gov / gene / 706985). For example, the human α-syn gene consists of the human α-syn gene (gene ID: 6622 (https: / / www.ncbi.nlm.nih.gov / gene / 6622)).

[0047] The term "at least one" as used herein refers to an amount of one, two, three or more of the indicated object, such as a conserved sequence as described herein.

[0048] The term "conserved sequence" or "conserved region" as used herein refers to a short stretch of sequence that can be found in various species with a high level of similarity. Conserved sequences can be identified by aligning multiple nucleic acid sequences from various species to code for RNA or proteins with similar functions, such that some or most of the sequence is identical.

[0049] Each of exons 2, 3, 4, 5 and 6 in the alpha-syn gene contains at least one conserved region for designing a target RNA to which the guide strand can bind. Preferably, the exons are selected from the group consisting of exons 2, 4 and 6. Multiple conserved sequences have been found to be present in exons 2, 4 and 6 of the NHP alpha-syn gene and / or the human alpha-syn gene. Thus, the exons are useful for designing the RNA.

[0050] Preferably, the guide strand binds to the target RNA encoded by part of exon 2 or exon 4, more preferably by part of exon 4. In other words, the target RNA sequence is part of exon 2, exon 4 or exon 6; preferably part of exon 2 or 4; more preferably part of exon 4.

[0051] The transcript of the target RNA, designed based on conserved sequences in exon 2, exon 4 and / or exon 6, can be reduced and / or knocked down by the guide strand, as described below.

[0052] The term "transcript" as used herein refers to the mRNA, protein and / or protein aggregates encoded by the alpha-syn gene. The terms "alpha-syn aggregates," "aggregates of alpha-syn protein," and / or other variants as used herein refer to aggregates composed of alpha-syn protein.

[0053] Any exon contained in the α-syn gene that contains at least a conserved sequence, such as exon 3 and / or exon 5, is also encompassed by the present invention.

[0054] More preferably, said portion of said exon as described above is selected from the group consisting of SEQ ID NOs: 3 to 9 (Table 1) and variants of SEQ ID NOs: 3 to 9, preferably selected from the group consisting of SEQ ID NOs: 4, 7 and 8 and variants of SEQ ID NOs: 4, 7 and 8, more preferably selected from the group consisting of SEQ ID NOs: 4 and 8 and variants of SEQ ID NOs: 4 and 8. In other words, said portion of said exon consists of a sequence selected from the group consisting of SEQ ID NOs: 3 to 9 and variants of SEQ ID NOs: 3 to 9.

[0055] [Table 1]

[0056] The variants of SEQ ID NOs: 3-9 have substantially the same sequence and function as SEQ ID NOs: 3-9, respectively. The variants can be bound by a guide strand as described below, after which the target RNA and its transcripts, e.g., proteins, are reduced and / or knocked down. The variants of SEQ ID NOs: 3-9 have at least one nucleotide and up to five nucleotides that differ from SEQ ID NOs: 3-9, respectively.

[0057] The term "variant" as used herein refers to a variant of the target RNA sequence that has substantially the same function as the target sequence, respectively. Also, the variant of the guide strand described below has substantially the same function as the guide strand described below. That is, the variant of the guide strand can still bind to the target RNA or the variant of the target RNA to further inhibit and / or reduce the transcript encoded by the α-syn gene. Optionally, the variant of the target RNA sequence comprises up to 4 nucleotides, up to 3 nucleotides, up to 2 nucleotides, or at least 1 nucleotide, respectively, that differ from the target RNA sequence.

[0058] Preferably, the RNA sequence substantially complementary to the target RNA is selected from the group consisting of SEQ ID NOs: 10 to 16 (Table 2) and variants of SEQ ID NOs: 10 to 16, preferably selected from the group consisting of SEQ ID NOs: 11, 14 and 15 and variants of SEQ ID NOs: 11, 14 and 15, more preferably selected from the group consisting of SEQ ID NOs: 11 and 15 and variants of SEQ ID NOs: 11 and 15. Thus, the RNA sequence comprises a sequence selected from the group consisting of SEQ ID NOs: 10 to 16 and variants of SEQ ID NOs: 10 to 16.

[0059] [Table 2]

[0060] As described above, the RNA sequence that is substantially complementary to the target RNA sequence (i.e., the guide strand) is designed such that the RNA sequence binds to the target RNA sequence, thereby reducing and / or knocking down transcripts, such as mRNA, and / or protein of the alpha-syn gene.

[0061] The variants of SEQ ID NOs: 10 to 16 have substantially the same sequences of SEQ ID NOs: 10 to 16 and have substantially the same function and binding to the target DNA as SEQ ID NOs: 10 to 16, respectively. Optionally, the variants of SEQ ID NOs: 10 to 16 have at least one nucleotide and up to five nucleotides that differ from SEQ ID NOs: 10 to 16, respectively. Optionally, the variants of SEQ ID NOs: 10 to 16 include up to four nucleotides, up to three nucleotides, up to two nucleotides or at least one nucleotide that differs from SEQ ID NOs: 10 to 16, respectively.

[0062] Exemplary sequences of pri-miRNA scaffolds of the invention, including SEQ ID NOs: 10-16, are shown in Table 3.

[0063] [Table 3]

[0064] DNA molecules and expression cassettes A second aspect of the invention relates to a nucleic acid of the invention which is a DNA molecule ("a DNA molecule of the invention"). According to the invention, preferably a DNA molecule is provided. The DNA molecule comprises in one of its strands a sequence which corresponds to said nucleic acid sequence above.

[0065] Said DNA molecule may be useful to carry said nucleic acid sequence as described above and may be included in an AAV for transduction in a target organ as described above.

[0066] Preferably, said DNA molecule comprises a DNA expression cassette, said DNA expression cassette comprising: said nucleic acid sequence as described above; a promoter and a polyA tail; and said nucleic acid sequence is flanked at its 3' and 5' ends by inverted terminal repeats (ITRs). In other words, said DNA molecule is comprised in a DNA expression cassette, said DNA expression cassette further comprising a promoter and a polyA tail, and said nucleic acid is flanked by inverted terminal repeats (ITRs).

[0067] The term "DNA expression cassette" as used herein refers to a DNA nucleic acid sequence that includes a gene or nucleic acid sequence encoding an RNA molecule, a promoter, and a nucleic acid sequence encoding a polyA tail, said DNA expression cassette being flanked by ITRs and included in a viral vehicle that is then delivered to a target organ, such as the brain and / or other organs of the CNS.

[0068] The term "promoter" as used herein typically refers to a DNA sequence located 5' to a transcription initiation site for driving or initiating transcription of a linked nucleic acid sequence. In some embodiments of the invention, the promoter is a constitutive or ubiquitous promoter; a neuron-specific promoter; and / or a glial-specific promoter.

[0069] The constitutive promoter may be selected from the group consisting of a pol II promoter, a native or engineered chicken beta-actin promoter (CBA), a CAG promoter, a PGK promoter, a CMV promoter (e.g., as shown in Figure 2 of WO2016102664, which is incorporated herein by reference).

[0070] The term "glia-specific promoter" as described herein refers to a promoter that may be suitably used in increasing the expression of an exogenous nucleic acid and / or gene in glial cells, such as astrocytes, oligodendrocytes or microglial cells. For expression in astrocytes, GFAP may be used. For expression in oligodendrocytes, MBP, PLP, CNP or MAG may be used. For expression in microglia, CD68 or Hexb may be used. In some preferred embodiments of the present invention, the glia-specific promoter is an oligodendrocyte promoter selected from the group consisting of MBP, PLP, CNP and MAG, Preferably, the promoter is a neuron-specific promoter. The term "neuron-specific promoter" as used herein refers to a promoter that can be suitably used to increase the expression of an exogenous nucleic acid and / or gene in neuronal cells, such as brain cells.

[0071] Preferably, the neuron-specific promoter is selected from the group consisting of synapsin, neuron-specific enolase (NSE), human synapsin 1, CaMKII kinase, tubulin alpha (Hioki et al. Gene Ther. 2007 Jun;14(11):872-82) and platelet-derived growth factor beta chain (PDGF). More preferably, the promoter comprises a dopaminergic neuron-specific promoter. Preferably, the dopaminergic neuron-specific promoter is selected from TH (tyrosine hydroxylase) or Forkhead Box A2 (FOXA2).

[0072] The use of a neuron-specific promoter in the DNA expression cassette induces and / or enhances expression of the nucleic acid in the CNS, which is preferable to reduce and / or knockdown the transcript of the alpha-syn gene, since the transcript of the alpha-syn gene is expressed primarily in the CNS, e.g., the brain and spinal cord, and even more primarily in the brain, and even more primarily in neurons.

[0073] Other suitable promoters that can be included in the present invention are inducible and / or repressible promoters, ie, promoters that initiate transcription only when the host cell is exposed to a particular stimulus.

[0074] Optionally, the DNA expression cassette comprises at least two promoters, including those described above.

[0075] The term "polyA tail" as used herein refers to a long chain of adenine nucleotides that is added to an mRNA molecule to increase the stability of the RNA molecule. Preferably, the polyA tail is Simian Virus 40 polyadenylation (SV40 polyA; SEQ ID NO: 44), Bovine Growth Hormone (BGH) polyadenylation (BGH polyA; SEQ ID NO: 45), Human Growth Hormone polyadenylation (hGH polyA; SEQ ID NO: 79) or synthetic polyadenylation. More preferably, the polyA tail is BGH polyA (SEQ ID NO: 45) or hGH polyA; SEQ ID NO: 79.

[0076] Preferably, the polyA tail contained in the DNA expression cassette, as defined above, is operably linked to the 3' end of the RNA molecule, as defined above.

[0077] The term "inverted terminal repeat (ITR)" as used herein refers to sequences at the 5' and 3' ends of the DNA expression cassette that function in cis as origins of DNA replication and viral packaging signals. The ITRs are preferably selected from the group consisting of adeno-associated virus (AAV) ITR sequences. More preferably, the ITR sequences are both AAV1, both AAV2, both AAV5, both AAV6, both AAV7, both AAV8, or both AAV9 ITR sequences. Also more preferably, the ITR sequence at the 5' end of the DNA expression cassette is different from the ITR sequence at the 3' end of the DNA expression cassette, and the ITR sequence is selected from AAV1, AAV2, AAV5, AAV6, AAV7, AAV8, and AAV9 ITR sequences.

[0078] The ITRs are located at the left and right ends (i.e., 5' and 3' ends, respectively) of the nucleic acid sequence as described above. Preferably, the ITRs are selected from the group consisting of adeno-associated virus (AAV) ITR sequences. More preferably, the ITR sequences comprise AAV1, AAV2, AAV5, AAV6, AAV7, AAV8 or AAV9 ITR sequences. Optionally, the two ITR sequences comprise both AAV1, both AAV2, both AAV5, both AAV6, both AAV7, both AAV8 or both AAV9 ITR sequences. Also optionally, the ITR sequence at the 5' end of the nucleic acid sequence is different from the ITR sequence at the 3' end of the nucleic acid sequence, and the ITR sequence is selected from AAV1, AAV2, AAV5, AAV6, AAV7, AAV8, AAV9 ITR sequences.

[0079] AAV According to the present invention, there is provided an AAV vehicle comprising the DNA as described above ("AAV vehicle of the present invention").

[0080] The viral vehicle used to deliver the foreign genetic material, such as the nucleic acid or DNA, is part of the present invention.Such viral vehicles include alphavirus, flavivirus, herpes simplex virus (HSV), measles virus, rhabdovirus, retrovirus, Newcastle disease virus (NDV), poxvirus, picornavirus, lentivirus, adenovirus vector, preferably AAV gene delivery vehicle.

[0081] The term "AAV vehicle" as used herein refers to a wild-type or recombinant AAV that acts as a vehicle to deliver genetic material, such as a foreign nucleic acid, a gene of interest, a nucleic acid of interest, a vector comprising said foreign nucleic acid, a vector comprising said gene of interest, said DNA expression cassette as described above, and / or a vector comprising said DNA expression cassette as described above, to a target cell, organ and / or tissue.

[0082] AAV vehicle, as described above, has been found to be a useful viral vehicle for delivery of nucleic acid or DNA expression cassette to mammals. AAV vehicle has the ability to efficiently infect dividing and non-dividing human cells. Moreover, said AAV vehicle is not associated with any disease. Therefore, said AAV vehicle is useful in the present invention and for treating and / or preventing diseases involving alpha-syn gene, as described below.

[0083] According to the present invention, the AAV vehicle comprises a nucleic acid comprising a nucleic acid sequence encoding an RNA, wherein the RNA sequence comprised in the RNA is substantially complementary to a target RNA sequence encoded by an α-syn gene, wherein the RNA sequence has at least 15 nucleotides, and wherein the RNA comprises a hairpin comprising SEQ ID NO: 1, or SEQ ID NO: 2, or a variant of SEQ ID NO: 1 or 2. The RNA sequence substantially complementary to the target RNA sequence is selected from the group consisting of SEQ ID NOs: 10-16 and variants of SEQ ID NOs: 10-16, preferably SEQ ID NOs: 11, 14 and 15 and variants of SEQ ID NOs: 11, 14 and 15, more preferably SEQ ID NOs: 11 and 15, and variants of SEQ ID NOs: 11 and 15.

[0084] Also according to the invention, the AAV vehicle may comprise a further nucleic acid comprising a nucleic acid sequence encoding an RNA, the RNA sequence comprised in the RNA being substantially complementary to a target RNA sequence encoded by the α-syn gene, the RNA sequence having at least 15 nucleotides, the RNA comprising a hairpin comprising SEQ ID NO: 1, or SEQ ID NO: 2, or a variant of SEQ ID NO: 1 or 2. The RNA sequence substantially complementary to the target RNA sequence is selected from the group consisting of SEQ ID NOs: 10-16 and variants of SEQ ID NOs: 10-16, preferably SEQ ID NOs: 11, 14 and 15 and variants of SEQ ID NOs: 11, 14 and 15, more preferably SEQ ID NOs: 11 and 15 and variants of SEQ ID NOs: 11 and 15.

[0085] As mentioned above, the AAV vehicle for delivering the DNA expression cassette can modify and / or reduce the (over)expression level of the product encoded by the alpha-syn gene. Preferably, the AAV vehicle is used to reduce and / or knock down alpha-syn aggregates. The alpha-syn aggregates typically comprise the protein encoded by the alpha-syn gene.

[0086] The term "reduce" as used herein refers to a decrease or lowering of the level and / or amount of a given analyte. The term "knockdown" as used herein refers to a level and / or amount of a given analyte that is substantially depleted or eliminated.

[0087] Optionally, the AAV vehicle is used to reduce and / or knock down the transcript encoded by the mutant SNCA gene. Studies of families with a history of Parkinson's disease have led to the identification of a series of familial mutations that result in early-onset (A30P, E46K, A53T, G51D) or late-onset (H50Q) forms of the disease.

[0088] Preferably, the AAV vehicle is used to reduce and / or knock down at least one isoform, including but not limited to, an alpha-syn isoform encoded by SEQ ID NO:36 (SNCA140), SEQ ID NO:76 (SNCA126), SEQ ID NO:77 (SNCA112) or SEQ ID NO:78 (SNCA98). More preferably, the AAV vehicle is used to reduce and / or knock down at least one isoform encoded by an alpha-syn nucleic acid sequence comprising exons 2, 4 and / or 6.

[0089] More preferably, as described above, at least two of said RNAs aimed at reducing and / or knocking down the transcripts of different target RNAs can be combined in one AAV vehicle to further enhance the inhibitory effect on the transcripts of the alpha-syn gene, thus further improving the treatment and / or prevention of said diseases as described below.

[0090] In some embodiments of the invention, a combination of the RNA aimed at reducing and / or knocking down the target RNA having SEQ ID NO: 4 and the RNA aimed at reducing and / or knocking down the target RNA having SEQ ID NO: 8 can be combined in one AAV vehicle to further enhance the inhibitory effect on the transcript of the alpha-syn gene as described below.

[0091] Preferably, the AAV vehicle is an AAV5, AAV8, or AAV9 vehicle. More preferably, the AAV vehicle is an AAV5 or AAV9 vehicle or a hybrid thereof. The AAV vehicle of the present invention may also be an AAV2 / AAV5 or AAV2 / AAV9 hybrid capsid.

[0092] In some embodiments of the present invention, the AAV vehicle is an AAV5 vehicle. AAV5 is useful in the present invention because the prevalence of anti-AAV5 neutralizing antibodies (Nab) is lower than the prevalence of Nabs against other serotypes. Furthermore, pre-existing antibodies (Ab) or low pre-existing antibodies against AAV5 usually do not affect transduction by the AAV gene therapy vehicle and / or expression of the nucleic acid in target organs. Furthermore, no cytotoxic T cell response against AAV5 has been reported in clinical trials.

[0093] In some embodiments of the invention, the AAV vehicle is an AAV9 vehicle. AAV9 is useful for delivering exogenous nucleic acid to neuronal and glial cells, such as oligodendrocytes.

[0094] In some cases, the AAV vehicle includes a capsid derived from AAV1, AAV2, AAV3, AAV4, AAV5, AAV6, AAV7, AAV8, AAV9, AAVrhlO, AAV11, and variants thereof (e.g., capsid variants with amino acid insertions, additions and substitutions, or hybrid capsids).

[0095] Preferably, the AAV vehicles of the present invention comprise capsids comprising AAV5 and / or AAV9 and / or hybrid capsid protein sequences.

[0096] An AAV capsid typically contains a VP1 protein and two shorter proteins, termed VP2 and VP3, which are essentially amino-terminal truncations of VP1. The three capsid proteins VP1, VP2, and VP3 are typically present in the capsid in a ratio that approximates 1:1:10, respectively, although this ratio, particularly that of VP3, can vary and should not be considered limiting.

[0097] Further included in the present invention are other hybrid capsids with optimized VP 1:2:3 stoichiometry, which can improve the AAV vehicle in infectivity to target organs and correct virion assembly.

[0098] AAV vehicles having capsid proteins VP1, VP2 and VP3 in a ratio approximating 1:1:10 or an optimized VP 1:2:3 stoichiometry are useful for delivering foreign nucleic acid sequences and / or transducing target organs, such as those involved in PD, in human subjects.

[0099] As described herein and above, the AAV vehicle may be defined as a "hybrid", meaning that the viral ITRs and viral capsid are derived from different AAV serotypes. The viral ITRs are preferably derived from AAV2, and the capsid is derived from a different one, which may be preferably AAV5 or AAV9. Other hybrids, such as hybrids containing combinations of different serotypes of capsid and ITRs, as well as capsid elements from different serotypes, possibly with further ITRs, may also be used in the present invention.

[0100] Preferably, the AAV vehicle of the present invention is a gene therapy vehicle.

[0101] The term "gene therapy" as used herein refers to a therapy that has a more stable and / or long-lasting effect than existing therapies for treating and / or preventing diseases involving the alpha-syn gene. A preferred method for achieving a stable therapeutic effect is by a single administration of the AAV gene therapy vehicle. The stability of the therapy can be measured by common techniques known to scientists in the art. The long-term effect can be measured by the length of time the therapeutic effect lasts and / or by the amount of dose and / or frequency of injections required to maintain such therapeutic effect.

[0102] The term "treat" or "treatment" as described herein refers to any measure that can stop, alleviate, delay, slow down and / or ameliorate said disease and / or preferably at least one symptom caused by said disease, such as a neurological progressive disease, as described below. Such measures may include, but are not limited to, delaying and / or slowing the progression of a neurological progressive disease, stopping the development of at least one symptom, relieving the ailment caused by said disease, and / or improving the health status of the patient. The term "prevent" or "prevention" as described herein refers to any measure to stop the development of said disease, including but not limited to the development of new symptoms of said disease. The terms "disease" and "disorder" can be used interchangeably in the present invention.

[0103] The AAV gene therapy vehicle can provide a consistent effect on the expression level and / or activity level of the transcript. Thus, in some embodiments of the present invention, the AAV gene therapy vehicle can be used to provide a consistent and / or long-term therapeutic effect on the treatment and / or prevention of the diseases and / or conditions described below. Thereby, the quality of life of patients suffering from the diseases and / or conditions can also be improved by administering the AAV vehicle.

[0104] The long-term efficacy of the AAV gene therapy vehicle can be assessed by measuring improved outcomes of disease parameters over a long period of time compared to a disease and / or existing therapies for treating the disease.

[0105] composition According to the present invention there is provided a composition comprising said AAV vehicle as described above and at least one pharma- ceutically acceptable excipient.Preferably, said composition comprises said AAV gene therapy vehicle.

[0106] The composition may be in solid or liquid form, hi some embodiments of the invention, the composition is a formulation.

[0107] The term "additive" or "excipient" as described above and herein refers to a substance that is further added to the composition to provide at least one function to the composition, including but not limited to supplementing the properties of the composition, stabilizing the composition for easy storage and / or extended shelf life, inhibiting side effects such as immune response, improving the transduction efficacy of the AAV vehicle to the target organ, and / or improving bypass of the blood-brain barrier (BBB). The present invention can further include additives or excipients that act as bulking agents without changing and / or affecting the properties of the composition.

[0108] Pharmaceutically acceptable excipients for administering AAV gene delivery vehicles are well known to those skilled in the art and can be as simple as water for injection. They can also include surfactants, osmotic agents, antioxidants, and the like.

[0109] Optionally, the composition further comprises an immunosuppressant compound. The immunosuppressant compound can reduce and / or prevent the immune response induced by the injection of the viral vehicle. The immunosuppressant compound can also be administered separately from the AAV composition. Such a combination is included in the present invention as a kit.

[0110] Optionally, a compound for improving biodistribution of the RNA in the brain, such as the hairpin, is further included in the composition.

[0111] Optionally, the composition further comprises at least one additive selected from the group consisting of an aqueous liquid, an organic solvent, a buffer, and an excipient. Optionally, the aqueous liquid is water. Optionally, the buffer is selected from the group consisting of acetate, citrate, phosphate, Tris, histidine, and 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES). Optionally, the organic solvent is selected from the group consisting of ethanol, methanol, and dichloromethane. Optionally, the excipient is a salt, a sugar, cholesterol, or a fatty acid. Optionally, the salt is selected from the group consisting of sodium chloride and potassium chloride, as described above. Optionally, the sugar is sucrose, mannitol, trehalose, and / or dextran, as described above.

[0112] The term "target organ" as used herein refers to an organ in which the transcript of the alpha-syn gene accumulates. For example, the target organ is the brain of a human subject. Other organs contained in the CNS (i.e., the brain and spinal cord) can also be included in the present invention, provided that the alpha-syn transcript, such as aggregates, is present in the organ.

[0113] Purpose The present invention provides the use of said AAV (vehicle) and / or said AAV gene therapy vehicle as described above as a medicament. Accordingly, the present invention also provides the use of said composition as a medicament.

[0114] The terms "AAV" and "AAV vehicle" are used interchangeably herein. The AAV vehicle (and / or the composition comprising the AAV vehicle) as described above can reduce and / or knock down the transcript of the alpha-syn gene. The AAV vehicle is thereby useful for treating and / or preventing a disease caused by the transcript of the alpha-syn gene, typically a disease caused by overexpression of the transcript encoded by the alpha-syn gene and / or caused by an aggregated protein encoded by the alpha-syn gene.

[0115] The transcript is an mRNA and / or a protein, preferably an mRNA. Thereby, the AAV vehicle and the composition are useful (i.e., have a therapeutic effect) in the treatment and / or prevention of a disease in which the alpha-syn gene is involved. Thus, according to the present invention, the AAV vehicle and / or the composition as described above are for use as a medicament in the treatment and / or prevention of a disease in which the alpha-syn gene is involved.

[0116] The disease and / or condition in which the alpha-syn gene is involved or caused by a transcript encoded by the alpha-syn gene (e.g., by overexpression of the transcript) is preferably a disease caused by overexpression of the alpha-syn protein and / or aggregates of alpha-syn protein.

[0117] In some embodiments of the invention, the AAV vehicle and / or the AAV gene therapy vehicle and / or composition as described above is used to treat and / or prevent a disease by reducing and / or knocking down the transcript encoded by the alpha-syn gene.Accordingly, the invention also provides the use of the AAV vehicle and / or the AAV gene therapy vehicle and / or composition as described above as a medicament, wherein the medicament reduces and / or knocks down the transcript encoded by the alpha-syn gene.

[0118] The disease may further include a disease involving at least one single nucleotide polymorphism (SNP) in the alpha-syn gene, for example, the disease is caused by a protein and / or aggregate that encodes at least one SNP in the alpha-syn gene.

[0119] Preferably, the alpha-syn protein (SEQ ID NO: 35) expression level is reduced by at least 30% and / or up to 70% compared to the alpha-syn protein expression level in the absence of administration of the AAV vehicle and / or the composition. More preferably, the protein encoded by the SNCA gene is reduced by up to 50% compared to the endogenous alpha-syn protein expression level in the absence of administration of the AAV vehicle and / or the composition. Complete knockdown may not be preferred due to the central role of the alpha-syn gene.

[0120] Preferably, the AAV vehicle and / or composition as described above can reduce the transcripts as described above by at least about 30% and / or up to 70%, more preferably up to 50%, compared to when the AAV vehicle and / or composition is not administered to a human subject.

[0121] Preferably, the expression level of the transcript is reduced by at least 30% and up to 70%, more preferably up to 50%, compared to the expression level in the absence of administration of the AAV vehicle and / or the composition. More preferably, α-syn protein is reduced by at least 30% and up to 70%, even more preferably up to 50%, compared to the α-syn protein level in the absence of administration of the AAV vehicle and / or the composition.

[0122] Preferably, the expression level of the transcript is reduced by at least 30% and at most 70%, more preferably by up to 50%, compared to the expression level in the absence of administration of the AAV vehicle and / or the composition to a human subject. More preferably, α-syn protein is reduced by at least 30% and at most 70%, even more preferably by up to 50%, compared to the α-syn protein level in the absence of administration of the AAV vehicle and / or the composition to a human subject.

[0123] By using the AAV vehicle, the level of the transcript of the alpha-syn gene is reduced but not completely substantially depleted, thus at least partially treating and / or preventing diseases caused by overexpression of the transcript and / or aggregates of alpha-syn protein, and also at least partially treating and / or preventing diseases and / or symptoms caused by complete knockdown of the transcript.

[0124] In some embodiments of the invention, the AAV vehicle and / or the composition are used to reduce and / or knock down alpha-syn protein aggregates, which typically comprise a protein encoded by the alpha-syn gene.

[0125] Preferably, the α-syn aggregates are reduced by at least 30% and / or up to 70%, more preferably up to 50%, compared to the amount of α-syn aggregates in a patient / human subject not administered the AAV vehicle and / or composition.

[0126] Although reducing and / or knocking down the transcript encoded by the alpha-syn gene is beneficial, complete depletion (i.e., complete knockdown) may result in impaired synaptic transmission and / or neurodegeneration in the CNS, potentially putting the patient at risk.

[0127] Thereby, the AAV vehicle and / or the composition are useful in treating and / or preventing diseases in which the alpha-syn gene is involved, alleviating and / or preventing diseases and / or symptoms, but without causing a substantially complete knockdown, reducing and / or avoiding the risks caused by complete depletion of the transcript encoded by the alpha-syn gene.

[0128] The AAV vehicles and / or compositions as described above can be used for the treatment and / or prevention of the diseases caused by the formation and / or presence of oligomeric α-syn, fibrillar α-syn, aggregated α-syn, phosphorylated α-syn, Lewy bodies and / or Papp-Lantos bodies.

[0129] Preferably, said AAV vehicle and / or said composition as described above are used to reduce and / or knock down the amount of Lewy bodies and / or Papp-Lantos bodies.

[0130] Alpha-syn protein / aggregates form the majority of Lewy bodies and Papp-Lantos bodies (also known as Papp-Lantos inclusion bodies). Thus, by reducing and / or knocking down alpha-syn protein, the amount and / or progression of Lewy bodies and / or Papp-Lantos bodies can be reduced and / or eliminated. Thus, by using said AAV vehicle and / or said composition, the accumulation of Lewy bodies and / or Papp-Lantos bodies can be reduced to achieve treatment and / or prevention of diseases and / or conditions, as described below.

[0131] Thus, the AAV vehicle and / or the composition can be used as a pharmaceutical to reduce the amount of total α-syn, oligomeric α-syn, aggregated α-syn and phosphorylated α-syn, and thus the levels of Lewy bodies and Papprantau bodies, thereby halting disease progression and / or ameliorating disease symptoms.

[0132] Such diseases and / or conditions include, but are not limited to, clinical symptoms of PD, LBD, MSA, neuropsychiatric symptoms, motor symptoms of PD, cognitive disorders, sleep disorders, autonomic disorders, and / or olfactory disorders. Motor symptoms or motor symptoms of PD include at least two of the following: limb stiffness, tremor, and / or impaired balance and / or coordination, or symptoms.

[0133] Clinical symptoms of PD include, but are not limited to, resting tremor, bradykinesia, rigidity and loss of postural reflexes, secondary motor symptoms (hypomania, dysarthria, dysphagia, sialorrhea, micrognathism, shuffling gait, fasting, freezing, dystonia, and / or glabellar reflex) and / or non-motor symptoms (e.g., autonomic dysfunction, cognitive / neurobehavioral abnormalities, sleep disorders, anosmia, paresthesias, and / or pain).

[0134] Clinical symptoms of LBD include, but are not limited to, movement disorders typical of PD, such as stiffness of the limbs, tremors, and / or impaired balance and / or coordination, intellectual disability, hallucinations, dysregulation of bodily functions (autonomic nervous system), sudden changes in attention and mood, cognitive problems, sleep disorders, attention fluctuations, and depression and apathy.

[0135] Clinical symptoms of MSA include, but are not limited to, movement disorders typical of PD such as sexual dysfunction, urinary dysfunction, REM sleep behavior disorder, orthostatic hypotension, gait dysregulation, parkinsonism, cerebellar features, multidomain autonomic failure, pyramidal signs and / or frontal executive dysfunction.

[0136] Thus, the AAV vehicle or composition for use as a medicament is used to treat and / or prevent clinical symptoms of PD, LBD, MSA, neuropathic symptoms, motor symptoms of PD, cognitive disorders, sleep disorders, autonomic disorders, and / or olfactory disorders. Preferably, said AAV vehicle and / or composition is used to treat and / or prevent PD, MSA and / or LBD. Preferably, said disease is PD and / or MSA.

[0137] Overexpression of the alpha-syn gene, aggregation of the alpha-syn protein, and / or the formation and / or presence of Lewy bodies are indicative of a patient suffering from PD. By using the AAV vehicle and / or composition as described, the transcript of the alpha-syn gene can be reduced and / or knocked down. Thereby, the AAV vehicle and / or composition is useful for treating and / or preventing PD.

[0138] Preferably, the AAV vehicles and / or compositions are used to treat and / or prevent pre-symptomatic or symptomatic PD patients.

[0139] The term "presymptomatic stage" as used herein refers to the stage of a neuronal progressive disease, such as PD, prior to the onset of clinical disease.

[0140] The term "symptomatic stage" as used herein refers to the stage of a neuronal progressive disease, such as PD, following clinical diagnosis of said disease.

[0141] PD patients usually realize that they have PD when they experience at least one of the symptoms as described above.However, because most of the neurons are lost at the pre-symptomatic stage, it may be too late to treat and / or prevent disease progression.Therefore, it is useful to have a treatment method, such as the use of the composition, in treating and / or preventing disease progression before at least one symptom of PD, such as motor symptoms, is shown.

[0142] As described above, the AAV vehicle and / or the composition can reduce α-syn protein levels, thereby making the AAV vehicle and / or the composition useful for treating and / or preventing at least one PD symptom, which can be selected from the group consisting of depression, sleep disorders, pain and fatigue in the early stages of the disease, and anxiety, dementia and cognitive impairment in the later stages of the disease.

[0143] Similarly, Lewy body deposits can cause a form of dementia called Lewy body dementia or LBD. In fact, LBD causes some or all of the motor symptoms of Parkinson's disease. Therefore, said AAV vehicle and / or said composition can also prove useful for treating and / or preventing at least one PD symptom.

[0144] Moreover, overexpression of the α-syn gene and / or the aggregated protein encoded by the α-syn gene may increase the risk of MSA, a progressive brain disorder that affects and / or impedes movement and balance and / or disrupts the function of the autonomic nervous system. The disease was originally known as Scheidlager syndrome. Currently, MSA is considered to be "sporadic," meaning that there is no established genetic or environmental factor that causes the disease.

[0145] Although many of the clinical symptoms are also present in patients with Parkinson's disease, those with MSA typically present with an onset of symptoms at a younger age, with the average onset being in the early 50s. Many patients are first diagnosed with Parkinson's disease, but over time, the extent, severity, and type of symptoms change, making a diagnosis of MSA more likely.

[0146] Important differences distinguish the symptoms and course of MSA from Parkinson's disease. In particular, MSA affects several areas of the brain, including the cerebellum, the balance and coordination center of the brain, and the autonomic nervous system, as described above. Furthermore, Parkinson's disease affects dopamine-producing neurons in the motor control part of the brain known as the nigrostriatal region, whereas MSA affects both neurons and glial cells.

[0147] In MSA, hyperphosphorylated α-syn is found in Papp-Lantos inclusions (or GCIs). Thus, the AAV vehicles and / or compositions of the present invention may also be useful in reducing and / or inhibiting the amount of Papp-Lantos inclusions and in treating and / or preventing MSA.

[0148] Other diseases, such as CNS diseases, can be treated and / or prevented by similar approaches using AAV vehicles and / or compositions comprising AAV vehicles, where the disease is caused by overexpression of a gene but where complete knockout of the transcript of the gene is less desirable.

[0149] Furthermore, at different stages (i.e., phases) of a progressive neurological disorder caused by the accumulation of alpha-syn gene transcripts, patients may develop different symptoms and / or different levels of disease, and the AAV vehicle and / or composition provide a solution for treating and / or preventing said different symptoms and / or different levels of disease without constantly modifying treatment regimens.

[0150] method According to the present invention, there is provided a method for producing the AAV vehicle as described above.

[0151] Optionally, said AAV vehicle can be produced by using mammalian cells.Optionally, said AAV vehicle can be produced by using insect cells, preferably baculovirus.Suitable methods for producing AAV gene therapy vehicles comprising the above-mentioned DNA expression cassettes are described in WO2007 / 046703, WO2007 / 148971, WO2009 / 014445, WO2009 / 104964, WO2011 / 122950, ​​WO2013 / 036118, which are incorporated herein in their entirety and are particularly referred to for their production methods.Optionally, said composition further comprises said immunosuppressant compound.

[0152] According to the present invention there is provided a method for making the composition as described above.

[0153] kit For the purpose of treating and / or preventing a disease or disorder as above, the AAV vehicle and at least one additive as above can be combined in a kit, which can optionally comprise a means for holding and / or containing the AAV vehicle and at least one additive.

[0154] In some embodiments of the invention, the kit comprises an AAV vehicle of the invention and an immunosuppressant compound as described above, and medical personnel and patients can easily apply the AAV vehicle to a human subject according to the label and / or instructions.

[0155] It is understood that a kit is also provided that includes a composition comprising the AAV vehicle of the present invention and at least one pharma- ceutically acceptable excipient. Optionally, the kit further includes at least one additive selected from the group consisting of an aqueous liquid, an organic solvent, a buffer, and an excipient. Optionally, the aqueous liquid is water. Optionally, the buffer is selected from the group consisting of acetate, citrate, phosphate, Tris, histidine, and 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES). Optionally, the organic solvent is selected from the group consisting of ethanol, methanol, and dichloromethane. Additionally, the excipient is a salt, a sugar, cholesterol, or a fatty acid. Optionally, the salt is selected from the group consisting of sodium chloride, potassium chloride, as described above. Optionally, the sugar is sucrose, mannitol, trehalose, and / or dextran, as described above. [Brief description of the drawings]

[0156] [Figure 1] other splicing variants of SNCA mRNA (SNCA140, SNCA126, SNCA112, SNCA98), and within the region targeted by miSNCA candidate sequences (candidates 2, 5, 7, 12, 13, 15, 16). [Diagram 2] (A) Vector maps for the original expression cassette with only the miR451 backbone and (B) the improved expression cassette with miR144 included in the backbone. [Diagram 3] Dual-luciferase assay titration of miSNCA candidates [Figure 4] Dual luciferase assay: original and improved tTitration of miSNCA5 and miSNCA15. [Diagram 5] Dose-dependent reduction of endogenous α-syn in HEK293T cells at both the mRNA and protein levels. A significant correlation was observed between SNCA mRNA and a-syn protein levels. [Figure 6A]Expression levels of miSNCA5 relative to endogenous miRNAs. [Figure 6B] Expression levels of miSNCA15 relative to endogenous miRNAs. [Figure 7] miRNA processing of miSNCA5 and miSNCA15. [Figure 8] Plasmid pVD1502 Plasmid ap. [Figure 9A] Route of administration studies in wild-type (wt) rats. AAV5-GFP vDNA levels. [Figure 9B] Route of administration study in wild-type (wt) rats. AAV5-GFP mRNA expression relative to GAPDH as a housekeeping gene. [Figure 10-1] Mechanism of action study in a-syn KI rats. (A) vDNA levels; (B) miSNCA5 levels. [Figure 10-2] Mechanism of action study in a-syn KI rats. (C) miSNCA15 levels; (D) SNCA mRNA reduction in the striatum. [Figure 11] Rescue of motility phenotypes in C. elegans PD models by miSNCA candidates. [Figure 12] Processing of miRNA extracted from rat brain tissue from in vivo study #2 and pooled samples of Group 4 from this study. [Figure 13] Figure 1 shows vDNA levels in the striatum in in vivo study 3 (AAV1 / 2-ha53T-aSyn rat model of Parkinson's disease). vDNA levels were comparable in all groups receiving the same dose of AAV5-unrelated miR or AAV5-miSNCA treatment. [Figure 14] miSNCA levels in the striatum in in vivo study 3 (AAV1 / 2-ha53T-aSyn rat model of Parkinson's disease). (A) miSNCA5 levels were higher in the group injected with AAV5-miSNCA5; (B) miSNCA15 levels were higher in the group injected with AAV5-miSNCA15. [Figure 15]Human SNCA mRNA levels in the striatum in in vivo study 3 (AAV1 / 2-hA53T-aSyn rat model of Parkinson's disease): Human SNCA mRNA levels were highest in the AAV1 / 2-hA53T-aSyn groups co- or sequentially injected with AAV5-unrelated miR. Human SNCA mRNA levels were significantly lower in the AAV1 / 2-hA53T-aSyn groups co- or sequentially injected with AAV5-miSNCA5 or AAV5-miSNCA15. [Figure 16] Human α-syn protein levels in the striatum in in vivo study 3 (AAV1 / 2-Ha53T-aSyn rat model of Parkinson's disease). Human α-syn protein levels were highest in the AAV1 / 2-Ha53T-aSyn groups co- or sequentially injected with AAV5-unrelated miR. Human α-syn protein levels were significantly lower in the AAV1 / 2-HA53T-aSyn groups co- or sequentially injected with AAV5-miSNCA5 or AAV5-miSNCA15. [Figure 17] Striatal dopamine transporter levels (assessed by ([125I]-RTI-121 autoradiography) in in vivo study 3 (AAV1 / 2-hA53T-aSyn rat model of Parkinson's disease); dopamine transporter levels were significantly reduced (similar to those observed in PD patients) in the AAV1 / 2-hA53T-aSyn group that received sequential injections of AAV5-unrelated miRs. Sequential injections of AAV5-miSNCA5 or AAV5-miSNCA15 rescued the loss of dopamine transporter. [Figure 18]Dopamine and dopamine metabolite levels in the striatum (assessed by LC / MS) in in vivo study 3 (AAV1 / 2-hA53T-aSyn rat model of Parkinson's disease); (A) Dopamine levels were significantly decreased in the ipsilateral striatum of the AAV1 / 2-hA53T-aSyn group sequentially injected with AAV5-unrelated miR (similar to that observed in PD patients). Sequential injection of AAV5-miSNCA5 or AAV5-miSNCA15 rescued the dopamine loss. (B) The ratio between dopamine metabolites and dopamine was significantly increased in the ipsilateral striatum of the AAV1 / 2-hA53T-aSyn group sequentially injected with AAV5-unrelated miR, indicating a deficit in dopamine turnover (similar to that observed in PD patients). Successive injections of AAV5-miSNCA5 or AAV5-miSNCA15 rescued the loss of dopamine turnover. [Figure 19] Motor behavior testing (cylinder test, assessment of paw asymmetry) in in vivo study 3 (AAV1 / 2-hA53T-aSyn rat model of Parkinson's disease). (A) At baseline (before injection), there was no asymmetry in paw use in any treatment group; (B) In the AAV1 / 2-hA53T-aSyn group continuously injected with AAV5-unrelated miR, underuse of the contralateral paw was observed 56 days after treatment (similar to that observed in PD patients). Continuous infusion of AAV5-miSNCA5 or AAV5-miSNCA15 rescued this motor deficit. [Figure 20-1](A) TH and (B) human a-syn in the substantia nigra of in vivo study 3 (AAV1 / 2-hA53T-aSyn rat model of Parkinson's disease) assessed by immunohistochemistry; only the sequential injection group was evaluated. (A) Substantia nigra TH positive cells were significantly reduced in AAV1 / 2-hA53T-aSyn animals sequentially injected with AAV5-unrelated miR versus AAV1 / 2-empty vector animals sequentially injected with AAV5-unrelated miR (similar to what is observed in PD patients). Sequential injection of AAV5-miSNCA5 or AAV5-miSNCA15 rescued TH neuron loss. (B) Substantia nigra a-syn positive cells were reduced by AAV5-miSNCA5 or AAV5-miSNCA15, confirming target engagement. [Figure 20-2] (C) a-syn positive TH neurons in the substantia nigra of in vivo study 3 (AAV1 / 2-hA53T-aSyn rat model of Parkinson's disease) assessed by immunohistochemistry; only the sequential injection group was evaluated. (C) TH positive cells in the substantia nigra had significantly lower a-syn expression in the AAV5-miSNCA5 or AAV5-miSNCA15 treated groups. [Figure 21-1] Reduction of SNCA mRNA and α-syn protein expression in a C. elegans PD model by miSNCA candidates, assessed by RT-qPCR and Western blot, respectively. (A) SNCA mRNA levels, treated at L1 stage and measured at day 1; (B) SNCA mRNA levels, treated at L4 stage and measured at days 1, 4, 8, and 11; (C) SNCA mRNA levels, treated at day 1 and measured at days 1, 4, 8, and 11. Both SNCA mRNA and α-syn protein levels were reduced by miSNCA candidates compared to the EV-treated group. [Figure 21-2]Reduction of SNCA mRNA and α-syn protein expression in a C. elegans PD model by miSNCA candidates, assessed by RT-qPCR and Western blot, respectively. (D) α-syn protein levels, treated at L1 stage and measured at day 1; (B) α-syn protein levels, treated at L4 stage and measured at days 1, 4, 8, and 11; (C) α-syn protein levels, treated at day 1, and measured at days 1, 4, 8, and 11. Both SNCA mRNA and α-syn protein levels were reduced by miSNCA candidates compared to the EV-treated group. [Figure 22] Locomotor phenotype rescue in a C. elegans PD model by miSNCA candidates following treatment at the (A) L1, (B) L4 or (C) day 1 stage. [Figure 23-1] Small RNA sequencing results of C. elegans samples treated with full-length SNCA RNAi, miSNCA5 and miSNCA15 miRNAs at the L1 stage and collected at 1 and 4 days after treatment in their adult stages. (A) miSNCA5 and (B) miSNCA15 are correctly processed and can be found in the relevant samples. (C) miSNCA5 and miSNCA15 sequences in full-length SNCA treated C. elegans samples as well as all other designed miSNCAs (miSNCA2, miSNCA7, miSNCA12, miSNCA13, miSNCA16). [Figure 23-2] This is a continuation of Figure 23-1.

[0157] Examples of the present invention Materials and Methods Design of the SNCA miRNA guide strand. miSNCA (miRNA guide strand) was designed to target the common RNA sequence of the most common SNCA mRNA variants; SNCA140, SNCA126, SNCA112 and SNCA98. miRNA was designed in the region common to all of the major mRNA variants of SNCA (Figure 1) (McLean et al. 2012 Mol and Cell Neuroscience 49(2)230-239). The target region of the SNCA mRNA sequence is part of exon 2, exon 4 and exon 6. The most common SNP (A30P) outside these exons was avoided from being included in the guide RNA. Each of the conserved sequences was used to generate several different guide strands with 22 nucleotides (nt). Seventeen guides targeting SNCA were designed and integrated into the miR451 scaffold: miSNCA2 (SEQ ID NO: 24), miSNCA5 (SEQ ID NO: 25), miSNCA7 (SEQ ID NO: 26), miSNCA12 (SEQ ID NO: 27), miSNCA13 (SEQ ID NO: 28), miSNCA15 (SEQ ID NO: 29), miSNCA16 (SEQ ID NO: 30), miSNCA1 (SEQ ID NO: 80), miSNCA3 (SEQ ID NO: 81), miSNCA4 (SEQ ID NO: 82), miSNCA6 (SEQ ID NO: 83), miSNCA9 (SEQ ID NO: 84), miSNCA10 (SEQ ID NO: 85), miSNCA11 (SEQ ID NO: 86), miSNCA14 (SEQ ID NO: 87), miSNCA18 (SEQ ID NO: 88), miSNCA19 (SEQ ID NO: 89). These constructs contained only miR451 as the scaffold, not the miR144 helper. These were tested in vitro for their efficacy in reducing the expression of the linked SNCA reporter gene (SEQ ID NO: 34) in a dual-luciferase reporter plasmid using a dual-luciferase assay. Among these 17 miRNAs, 7 miRNAs (miSNCA2, miSNCA5, miSNCA7, miSNCA12, miSNCA13, miSNCA15 and miSNCA16 pri-miRNAs; SEQ ID NO: 17-23) encoded in ITR-containing vectors (SEQ ID NO: 24-30) showed the potential to reduce SNCA mRNA levels in a dose-dependent manner (Figure 3).

[0158] miSNCA guides were selected based on the following criteria: miRNA guide sequences should not contain stretches of >4 G, >4 C, >5 A and >5T nt; GC content of 30%-70%; less than 4000 predicted off-target genes of miRNA seed sequence for exon 1a targeting guides and less than 5000 predicted off-target genes of miRNA seed sequence for intron 1 targeting guides by using siSPOTR analysis (https: / / sispotr.icts.uiowa.edu. / sispotr / tools / lookup / evaluate.html); and pre-miRNA sequence folding energy of -44 kcal / mol to -55 kcal / mol). To generate a negative control, a scrambled guide was designed for in vitro testing and named miSCR (SEQ ID NO: 90).

[0159] The selected miSNCA guides fulfilled the following criteria: conservation with the monkey SNCA gene sequence (Macaca mulatta, NCBI accession number NC_041768.1); the miRNA guide sequence did not contain a stretch of >4 G or >4 C nt; GC content between 20% and 70%; GC seed content between 40% and 70%; pre-miRNA sequence folding energy between -45 kcal / mol and -55 kcal / mol; and no matches with endogenous miRNA seeds.

[0160] Guide sequences were incorporated into the human pri-miRNA miR-451 scaffold sequence and the mFold program (http: / / unafold.rna.albany.edu / ?q=mfold) was used with standard settings to determine whether the candidates folded into a secondary structure.

[0161] The original SNCA scaffold (scaffold 1) consists of only one miR451 as a scaffold. The improved SNCA scaffold (scaffold 2) consists of a miR-144 hairpin and one mir-451 downstream scaffold. Scaffold 2 is an improved version of the original construct, containing miR144, which is a helper for the processing of miSNCA. The placement of the miR144 hairpin is always at the 5' end of the miR451 hairpin sequence (compared to the miR451 hairpin sequence, which is mostly). Seven SNCA constructs (scaffold 1) (sequence numbers 37-43) were made to target SNCA mRNA, and two improved SNCA constructs (scaffold 2) were generated to target different parts of SNCA mRNA (sequence numbers 91 and 92).

[0162] Dual reporter luciferase assay HEK293T cells were used for the dual luciferase assay and endogenous α-syn reduction. For the dual luciferase assay, HEK293T cells (1 × 10 5 Cells (1000 ng / well) were seeded in triplicate in 24-well tissue culture treated plates. Cells were co-transfected with a reporter plasmid (SEQ ID NO: 33) with a concatenated SNCA reporter sequence (SEQ ID NO: 34) (10 ng) and various amounts (0.1-1-10-100 ng) of plasmids carrying miSNCA candidates using Lipofectamine 3000 (Thermo Fisher Scientific). Cells were then harvested 2 days after transfection and cell samples were analyzed for Renilla luciferase and firefly luciferase activity using Promega's Dual Luciferase assay kit. Assays were performed in a GloMax Luminescence reader. α-syn reduction was measured as a decrease in the RL / FL activity ratio. Experiments were repeated an average of three times.

[0163] Transfection and reduction of endogenous α-syn To evaluate endogenous α-syn reduction by miSNCA candidates, HEK293T cells were used. For these assays, HEK293T cells (5 × 105 Cells / well) were seeded in triplicate in 6-well tissue culture-treated plates. Cells were transfected with various amounts (50-200-1000ng) of plasmids carrying miSNCA candidates using Lipofectamine 3000 (Thermo Fisher Scientific). Cells were then harvested 2 days after transfection. Cell samples were analyzed for SNCA mRNA levels and α-syn protein levels. Experiments were repeated an average of three times.

[0164] DNA constructs for baculovirus seed generation Expression cassettes carrying the different miSNCA constructs were subcloned into the ITR containing plasmids to generate pVD1496 (SEQ ID NO: 37), pVD1497 (SEQ ID NO: 38), pVD1498 (SEQ ID NO: 39), pVD1499 (SEQ ID NO: 40), pVD1500 (SEQ ID NO: 41), pVD1501 (SEQ ID NO: 42) and pVD1502 (SEQ ID NO: 43; Figure 8).

[0165] All of these pVD plasmids carry the CAG promoter and an intron required for promoter activity, followed by the miSNCA construct in the miR451 backbone (SEQ ID NOs: 24-30) and the bGH polyA sequence (FIG. 2A).

[0166] Improved construct versions of miSNCA5 and miSNCA15 were also generated by incorporating the miSNCA5 or miSNCA15 guide sequence into miR451 downstream of the miR144 helper miRNA (a scaffold containing miR144 and miR451; FIG. 2B), thus generating miR144-miSNCA5 (SEQ ID NO: 31) and miR144-miSNCA15 (SEQ ID NO: 32). These expression cassettes were subcloned into pVD1587 (SEQ ID NO: 91) and pVD1588 (SEQ ID NO: 92), which contain the ITR regions for AAV5 packaging.

[0167] AAV5 vectors Recombinant AAV5 carrying the expression cassette was produced by infecting SF+ insect cells (Protein Sciences Corporation, Meriden, Connecticut, USA) with two baculoviruses encoding Rep, Cap and Transgene. The titer of purified AAV was determined using QPCR according to standard protein purification procedures on a fast protein liquid chromatography system (AKTA Explorer, GE 30 Healthcare) using AVB Sepharose (GE Healthcare).

[0168] In vitro models and transduction assays To measure the effect of AAV5-miSNCA on human α-syn mRNA and protein levels, we used patient-derived iPSC-derived dopaminergic neurons (DA neurons). iPSC cell lines (Table 4) were obtained from the NINDS RUCDR repository.

[0169] [Table 4]

[0170] iPSC cells were differentiated into DA neurons using the PSC Dopaminergic neuron Differentiation kit from Thermo Fisher Scientific.

[0171] The in vitro cell model described above was transduced with baculovirus-produced AAV5-miSNCA candidates at various multiplicities of infection (MOI) of the virus. Cells were transduced with 5 × 10 5 Cells were seeded at 10 cells / well onto PDL-laminin or PLO-laminin-coated 6-well plates. After 3–4 days of subculture, cells were cultured at 10 4 , 10 5 , 10 6 and 10 7Cells were transduced at an MOI of 100 / cell. Cells were then harvested 7-15 days post-transduction. Cell samples were used for RNA and DNA isolation to determine vector DNA levels, miSNCA expression, SNCA mRNA and a-syn protein expression.

[0172] RNA Isolation and Small RNA Sequencing Using Next-Generation Sequencing (NGS) a. From HEK-produced AAV5-miSNCA candidates RNA was isolated from AAV5-miSNCA (HEK-produced)-transduced DA neurons (MOI was 10) using the Allprep DNA / RNA Micro kit (Qiagen). 6 Small RNAs were isolated from 1000 cells (100 / cell). RNA integrity was determined using Bioanalyzer and RNA was quantified using Nanodrop. Samples were then sent to GenomeScan BV (Leiden, The Netherlands) for small RNA sequencing. Small RNA sequencing was performed by GenomeScan using the NebNext small RNA library preparation method, including BluePippin size selection of the final library combined with Illumina NovaSeq 6000 PE 150 sequencing. Data were analyzed using CLC Genomics Suit (Qiagen). Expression values ​​of miSNCA candidates were expressed as RNA counts of miSNCA candidates relative to the total annotated miRNA sequence counts. Processing of miSNCA candidates was analyzed by aligning miSNCA raw pri-miRNA sequences against sequenced RNA molecules. MiSNCA molecules of various sizes and their counts were obtained.

[0173] b. Baculovirus-produced AAV5-miSNCA candidate RNA is isolated from AAV5-miSNCA candidate (baculovirus production) transduced cells (DA neurons, forebrain neurons and / or LUHMES-derived DA neurons) using Zymogen RNA isolation kit. RNA quality is determined using Bioanalyzer and RNA is quantified using Nanodrop. Samples are then sent to GenomeScan BV (Leiden, Netherlands) for small RNA sequencing using next-generation sequencing method. Data is analyzed using CLC Genomics Suit (Qiagen) to extract information on expression value of miSNCA candidate and also to find out the processing of miSNCA candidate expressed from baculovirus-produced AAV5-miSNCA candidate.

[0174] RNA was isolated from rat brain striatal samples from in vivo study #2, group #4 (described below). These animals were injected with both AAV5-miSNCA5 and AAV5-miSNCA15 in the striatum, and the processed sequences were found in the sequencing analysis of the samples. RNA was isolated using an AllPrep DNA / RNA isolation kit. RNA quality was tested using Bioanalyzer and quantified using Nanodrop. Samples were then sent to GenomeScan BV (Leiden, Netherlands) for small RNA sequencing using next-generation sequencing methods. Data was analyzed using CLC Genomics Suit (Qiagen) to evaluate the processing of miSNCA candidates expressed from baculovirus-produced AAV5-miSNCA candidates.

[0175] Small RNA Sequencing (NGS) Data Analysis Data analysis was performed using CLC Genomics Workbench 10 suit. Trimmed small RNA sequence reads were counted and annotated using the miRbase database. miSNCA molecules are annotated by aligning pri-miRNA sequences to these small RNA libraries. Expression values ​​of miSNCA candidates were expressed as the number of counts of miSNCA candidate counts over the total annotated small RNA counts. The most expressed miSNCA molecules were analyzed by examining the relative counts of miSNCAs of various sizes, aligning pre-miSNCAs to small RNA libraries, and using the RNA counts obtained therefrom.

[0176] Isolation and quantification of vector DNA from cells and animal tissues DNA extraction was performed using the AllPrep DNA / RNA Mini Kit (Qiagen) according to the manufacturer's instructions. Vector genome copies were quantified by using TaqMan qPCR assay (Thermo Fisher scientific) with primers against the polyA region of the vector. Quantification (GC / ug DNA) was performed using linearized pVD plasmid and preparing a standard curve with various amounts of this linearized plasmid. Using the standard curve thus prepared, vector DNA copy numbers were calculated from DNA isolated from cells transduced with AAV5-miSNCA.

[0177] Isolation of RNA and protein from transfected HEK cells and quantification of mSNCA and α-syn protein levels For RNA isolation, Direct-zol™ RNA Miniprep (Cat. No. R2050) was used. TRIzol was applied to the quick-frozen cell pellet for lysis. cDNA synthesis was performed using the Maxima First Strand cDNA Synthesis Kit for RT-qPCR (Thermo Fisher Scientific).

[0178] Protein isolation was performed using RIPA buffer (Sigma) containing PhosSTOP phosphatase inhibitors (Roche) and EDTA-free protease inhibitors (Roche). For protein extraction, buffer was added to the cell pellet and cells were stirred at 400 rpm for 30 min at 4C. The cell extract was then centrifuged at maximum speed. The clarified supernatant was used for α-syn and total protein measurements, i.e., HTRF and BCA assays.

[0179] For detection of mSNCA levels, a SYBR Green-based RT-qPCR assay was used using a primer set designed for SNCA (Table 5). Results were expressed as fold change using the ΔΔ cycle threshold (ΔΔCt) of treated versus untreated samples normalized to the average expression of housekeeping genes: UBE, CYC 1, and ACTB (Table 5).

[0180] [Table 5]

[0181] For detection of α-syn protein levels, a Total α-syn HTRF kit (Cisbio) was used. HTRF measurements were then normalized by the total protein added to the HTRF assay. Total protein measurements were performed using the bicinchoninic acid assay (BCA protein assay kit; Pierce™). HTRF results were expressed as HTRF ratio / μg total protein.

[0182] RNA isolation and quantification of miSNCA candidates, GFP mRNA and SNCA mRNA from animal tissues Tissues were homogenized using the Tissue Lyser system (Qiagen) and the AllPrep DNA / RNA Mini kit (Qiagen) according to the manufacturer's instructions. The quantity and integrity of DNA and RNA were determined by Nanodrop and Bioanalyzer.

[0183] For miSNCA expression, the following protocol was used: Total RNA was isolated using the AllPrep DNA / RNA Micro kit (Qiagen). RT-qPCR was performed using the Taqman stem-loop-miRNA assay (Thermo Fisher) designed to detect the 23 nt miSNCA5 and 22 nt miSNCA15. Expression levels were expressed as miRNA molecules / ug total RNA.

[0184] The assay IDs for these Taqman assays (Thermo Fisher) are: for miSNCA5_23nt, CTNKRV7; for miSNCA15_22nt, CTTZ9KY. For mRNA expression, total RNA was isolated using the AllPrep DNA / RNA Micro kit (Qiagen).

[0185] Two different RT-qPCR assays were used to measure SNCA and GFP mRNA expression: 1. SNCA or GFP mRNA expression was measured using a SYBR Green-based RT-qPCR assay. The genes used as housekeeping genes were: ACTB, B2M, GAPDH, HPRT. The primer sequences are shown in Table 6. 2. Taqman Assay for SNCA mRNA Primer and probe sequences designed for SNCA mRNA expression and Taqman ID for the ready-to-use Taqman assay for housekeeping genes are shown in Table 7.

[0186] [Table 6]

[0187] [Table 7]

[0188] LC-MS / MS from animal tissues Striatal tissue samples were shipped on dry ice to the Vanderbilt Neurochemistry Core Facility (Nashville, TN, USA) for determination of catecholamine levels, and data were shipped back to blinded Atuka for analysis.

[0189] Tissue Extraction Brain slices were cut into 10 pieces using a tissue dismembrator. -2 10 M sodium acetate -4 The cells were homogenized in 100-750 μl of 0.1 M TCA containing 1 M EDTA and 7.5% methanol (pH 3.8). 10 μl of homogenate was removed for protein concentration measurement. Samples were then spun in a microcentrifuge at 10,000 g for 20 min at 4°C. The supernatant was transferred to a new microcentrifuge tube for biogenic amine analysis.

[0190] Biogenic amine analysis Dopamine, HVA, and DOPAC levels were determined by a sensitive and specific liquid chromatography / mass spectrometry (LC-MS / MS) method after derivatization of the analytes with benzoyl chloride (BZC). Five μl of the supernatant was treated with 10 μl each of 500 mM NaCO3 (aq) and 2% BZC in acetonitrile. After 4 min, 13 The reaction was stopped by adding 10 μl of an internal standard solution (in 20% acetonitrile containing 3% sulfuric acid) containing 200 pg each of C6-derivatized dopamine-d4, HVA, and DOPAC. Liquid chromatography was performed on a 2.0 × 50 mm, 1.7 μm particle Acquity BEH C18 column (Waters Corporation, Milford, MA, USA) using a Waters Acquity UPLC. Mobile phase A was 0.15% formic acid in water and mobile phase B was acetonitrile. Samples were separated by a gradient of 98 to 5% mobile phase A over 11 min at a flow rate of 600 μl / min before delivery to a SCIEX 6500+QTrap mass spectrometer (AB Sciex, Framingham, MA, USA). The following MRM transitions were monitored for quantification purposes: 466 to 105, BZC-dopamine; 488 to 111, 13C6-BZC-dopamine-d4; 304 to 150, BZC-HVA; 310 to 111, 13 C6-BZC-HVA; 394 to 105, BZC-DOPAC; 406 to 111, 13 C6-BZC-DOPAC. Automated peak integration was performed using SCIEX Multiquant software version 3.0.2. All peaks were visually inspected to ensure proper integration. Peak area ratios (P 分析物 / P I.S. The levels of dopamine, HVA, and DOPAC in the samples were calculated by linear regression using a calibration curve constructed based on the concentration of the internal standard versus the concentration of the internal standard. Levels were normalized to the protein concentration in the tissue extracts.

[0191] Protein Assay Protein concentrations in tissue homogenates were determined using the Pierce™ BCA Protein Assay Kit (Thermo Fisher Scientific, MA USA) as described in the kit instructions provided. Absorbance was measured using a POLARstar Omega plate reader (BMG LABTECH, Offenburg, Germany).

[0192] ELISA of transgene-derived human α-syn Dissected striatal tissue from fresh frozen sections of all animals was homogenized in lysis buffer containing protease and phosphatase inhibitors (Roche: 11836153001). Samples were agitated for 30 min at 4°C and then centrifuged (135000 rpm for 10 min at 4°C) to generate the supernatant. A portion of the supernatant was used to determine total protein levels (BCA assay, Pierce, Rockford, IL) using a 1:500 dilution at a concentration of 0.001 mg / ml. Another portion of the supernatant was subjected to an ELISA procedure according to the manufacturer's instructions (BioLegend: 844101). Samples were analyzed using a CLARIOstar system that quantifies luminescence counts relative to the amount of aSyn. Levels of αSyn were expressed as pg / mg total protein (Pierce™ BCA Protein Assay Kit, Thermo Fisher Scientific, MA USA).

[0193] Dopamine transporter (DAT) binding The level of striatal DAT was assessed by [125I]-RTI-121 binding autoradiography in cryostat-cut sections prepared from 20 μm fresh frozen tissue. Briefly, thawed slides were placed in binding buffer containing 50 mM Tris, 120 mM NaCl and 5 mM KCl (2×15 min, room temperature). Sections were then placed in the same buffer containing 50 pM [125I]-RTI-121 (Perkin-Elmer, specific activity 2200 Ci / μmol) for 120 min at 25° C. to determine total binding. Nonspecific binding was defined as that observed in the presence of 100 μM GBR 12909 (Tocris Bioscience). All slides were then washed with ice-cold binding buffer (4×15 min), rinsed with ice-cold distilled water and air-dried. Slides were then mounted on autoradiography film (Kodak) along with [125I] microscale standards (Amersham) and left at room temperature for approximately 7 days before developing. Autoradiograms were then analyzed using MCID software (Image Research Inc, Ontario, Canada). Densitometric analysis of three striatum from each animal was performed and a reference curve of cpm vs. optical density was calculated from the β-emitting [14C] microscale standards and used to quantify the intensity of the signal as nCi / g. Background intensity was subtracted from each reading. Data were then expressed as the mean ± standard error signal intensity for each treatment group. Nonspecific binding was calculated in the same way and subtracted from the total to obtain specific binding. Nonspecific binding was typically found to account for less than 1% of the total binding.

[0194] Immunofluorescence and conformation Immunofluorescence: Brains were cryosectioned in the coronal plane at 40 μm thickness on a freezing slide microtome (Leica Microsystems Inc., Richmond Hill, ON), and six series of sections were stored in cryoprotectant (30% glycerol, 30% ethoxyethanol, 40% PBS). A single series of midbrain sections was used to perform double-label immunofluorescence to reveal hemagglutinin (HA)-tagged human aSyn and tyrosine hydroxylase (TH). Briefly, in free-floating sections, the levels and distribution of TH (sheep anti-TH, 1:1000, Pel Freez, P 60101; secondary antibody, Alexa fluor donkey anti-sheep, Fisher Scientific, A 21099, 1:500) and HA (rabbit anti-HA, 1:1000; Abcam, AB 9110; Alexa Fluor donkey anti-rabbit, 1:500, Fisher Scientific, A 21206, 1:500) were assessed by double-label immunofluorescence.

[0195] Three-dimensional structure: TH with and without human α-syn colocalization within the substantia nigra pars compacta (SNc) +veNeuronal number estimation was performed using Stereo Investigator software (MBF Bioscience, Williston, VT) according to stereological principles. Seven or eight sections separated by 240 μm from anterior to posterior SN, respectively, were used for counting in each case. Stereological analysis was performed using a Zeiss microscope (AxioImager M2 and Apotome, Carl Zeiss, Canada) coupled to a monochrome digital camera for visualization of tissue sections. The total number of TH+ve neurons with and without human α-syn inclusions was estimated from coded slides using optical fractionation. For each tissue section analyzed, section thickness was empirically evaluated and guard zones of approximately 2 μm thickness were used at the top and bottom of each section. The SNc was outlined under low magnification (5x) and TH+ve neurons were counted under 40x magnification. Stereo parameters were empirically determined (i.e., grid size, count frame size, and dissector height) using Stereo Investigator software (MicroBrightfield, VT, USA). The coefficient of error (CE) was calculated according to the procedure of West et al., known as Gunderson CE (m=1). Gunderson values ​​of less than 0.10 were accepted.

[0196] TH in the SNc to assess neuroprotection by counting stereology results +ve Absolute neuron counts were obtained. The number of remaining TH+ve neurons containing responsiveness to human α-synculin was also determined by the TH +ve These were generated to provide an indication of the number of human α-syn expressing neurons. +ve / Synuclein +ve :TH +ve / Synuclein -ve The ratio was calculated.

[0197] In vivo testing Test 1. Route of administration test in wild-type (WT) rats In this study, the distribution of transgene expression (GFP) was assessed 14 days after administration of AAV5-GFP into either the substantia nigra (SN), striatum or cisterna magna. Two treatment groups (total N=10, female Sprague-Dawley rats, Envigo, USA) with N=5 rats per group were used. On day 1, animals received bilateral 4 ul stereotactic injections of AAV5-GFP into the SN, 3x3ul (bilateral) stereotactic injections of AAV5-GFP into the striatum or 25ul injections of AAV5-GFP into the cisterna magna. Groups are shown in Table 8.

[0198] [Table 8]

[0199] For intra-SN injections, stereotaxic coordinates were -5.2mm AP and - / +2mm ML relative to bregma, the needle was lowered -7.5mm below the skull, and the tooth bar was set at -3.3. Striatal stereotaxic injection coordinates were site 1: +1.3mm AP, - / +2.8ML, -4.5DV; site 2: +0.2mm AP, - / +3.0ML, -5.0 DV; site 3: -0.6mm AP, - / +4.0ML, -5.5 DV; tooth bar was set at -3.3. Viral vectors were administered at a rate of 0.5ul / min, and a 5-minute waiting period was allowed after each injection. ICM administration was performed according to a method adapted from Chen et al. 2013 Acta Neurobiol Exp(Wars)73(2):304-11.

[0200] On day 14, rats were administered an overdose of isoflurane and sacrificed via transcardial perfusion with ice-cold 0.9% saline. Brains were then removed and the right hemisphere was post-fixed (overnight) in 4% paraformaldehyde and cryoprotected in sucrose solution. The right hemisphere forebrain and midbrain were then sectioned on a freezing slide microtome for histological procedures. The left hemisphere was freshly dissected into regions of interest and individually frozen for molecular analysis.

[0201] Study 2. Mechanism of action study in a-syn KI rats In this study, the mechanism of action of two AAV-miSNCA candidates was evaluated in human α-synuclein KI rats. A total of three treatment groups were used with N=3 animals per group (total N=9, Envigo, USA). On day 1, all animals received a 3x3ul unilateral injection of AAV5 into the striatum. The contralateral side served as a control and was injected with formulation buffer in the same manner as the AAV5 injection. Groups are shown in Table 9.

[0202] [Table 9]

[0203] Striatal stereotaxic injection coordinates were: Site 1: +1.3 mm AP, - / +2.8 ML, -4.5 DV; Site 2: +0.2 mm AP, - / +3.0 ML, -5.0 DV; Site 3: -0.6 mm AP, - / +4.0 ML, -5.5 DV; tooth bar set at -3.3. Viral vectors were administered at a rate of 0.5 ul / min and a 5 minute wait period was allowed after each injection.

[0204] On day 43, all rats were administered an overdose of isoflurane and perfused transcardially with ice-cold 0.9% saline. The brains were then removed as quickly as possible and divided into left and right hemispheres. In all animals in each group, the following regions were freshly dissected from the left and right hemispheres: prefrontal cortex, striatum, hippocampus, hypothalamus, thalamus, posterior cortex, cerebellum, ventral midbrain, and brainstem, frozen on dry ice, and stored at -80°C for molecular analysis.

[0205] Study 3. Study in the AAV-Syn Rat Model This study was designed to evaluate the ability of two artificial miRNAs (encoding aSyn) targeting SNCA mRNA to protect dopaminergic function in the AAV1 / 2-hA 53T-aSyn rat model of Parkinson's disease. This model involves unilateral injection of WT rats with AAV1 / 2 human A53T α-syn (AAV1 / 2-hA53T-aSyn) and AAV5-miRNA (either miSNCA or an unrelated (control) miRNA). Regarding the injection of these two viruses, there were two groups: a co-injection group and a sequential injection group. In the co-injection group, the two viruses were injected on day 1 (groups 1-4 in Table 10), and in the sequential group, AAV1 / 2-Ha53T-aSyn was injected on day 1 and AAV5-miSNCA was injected on day 14 (groups 5-8 in Table 10). Single viruses or combinations were administered unilaterally into the right substantia nigra following stereotactic techniques on the days indicated in Table 10. Behavioral assessments were performed in the cylinder test before surgery (baseline, day -3) and on days 14, 21, 42 and 56 (2, 3, 6 and 8 weeks after AAV administration) to assess forelimb asymmetry. Groups are shown in Table 10.

[0206] [Table 10]

[0207] [Table 11]

[0208] On day 57, the animals were sacrificed for post-mortem evaluation. Blood samples were collected, processed as required, and stored.

[0209] Primary endpoints of the study included: -Evaluation of forelimb asymmetry (by cylinder test) Quantification of striatal dopamine and metabolite levels (by LC-MS / MS) Quantification of dopamine transporters (by autoradiography) Quantification of transgene-derived aSyn levels in the striatum (by ELISA)

[0210] Any endpoints included: Quantification of tyrosine hydroxylase positive (TH+ve) cells in the substantia nigra with or without co-expression of human aSyn (by double-label immunofluorescence) Qualitative assessment of the activation state of microglia in the substantia nigra by Iba-1 immunoreactivity (by immunofluorescence)

[0211] Sacrifice and sampling were performed as follows: animals were deeply anesthetized with isoflurane and then killed by exsanguination via transcardial perfusion with ice-cold 0.9% saline containing 0.2% heparin. Brains were placed ventrally upwards into ice-cold stainless steel rat brain matrix and cut in the coronal plane, first at the level of the hypothalamus. The rostral part of the brain, including the entire striatum, was immediately frozen in isopentane cooled to -42°C and later sectioned for DAT autoradiography and dissected for quantification of dopamine and dopamine metabolites (HVA and DOPAC) levels by LC-MS / MS and human aSyn levels by ELISA. Tissues were stored in a -80°C lock freezer. Additional regions of interest (including additional striatal dissections) were collected according to Table 11 for molecular assays.

[0212] [Table 12]

[0213] The remaining caudal portion of the brain, including the midbrain, was immersed in 4% paraformaldehyde (PFA) for 48 hours for fixation and subsequently cryoprotected in graded sucrose solutions (15 to 30% sucrose). Tissue prepared in this manner was used for quantification of dopamine neuron numbers in the SNc via tyrosine hydroxylase immunohistochemistry and unbiased stereochemistry.

[0214] Test 4. Phenotypic rescue of the locomotor phenotype in a C. elegans PD model In this study, we evaluated the effect of expression of miSNCA candidates on the phenotypic rescue of altered locomotor behavior in a C. elegans PD model (OW 40; van Ham et al 2008 PLoS Genet 4(3):e 1000027). In this model, human α-syn is overexpressed in the body wall muscles of C. elegans. This α-syn overexpression slows down the movement of the worms when compared to control worms. The effect of reducing SNCA mRNA levels, and thereby reducing α-syn protein levels by RNAi, was studied using the full-length SNCA gene or our miSNCA constructs. Double-stranded RNA containing one of these constructs was introduced into the organism by feeding. OW 40 C. elegans were fed with the empty T 444T plasmid as a negative control, or E. coli overexpressing either the full-length SNCA gene or one of our miSNCA candidates (miSNCA5, miSNCA13 or miSNCA15) at different stages of their lifespan: larval stage 1 (L1), larval stage 4 (L4) and day 1 of their adult lifespan. Treatment experiments were repeated at 25°C and 15°C. After treatment at days 1, 4 and 8 of their adult lifespan, the worms were video tracked using a high-throughput tracking setup configured to measure their movement (speed as μm / sec) (Perni et al 2018 Journal of Neuroscience Methods 306 57-67).

[0215] Further readout was RT-qPCR of SNCA mRNA and α-syn protein levels using Western blot analysis. Primer sequences used for RT-qPCR of SNCA mRNA are shown in Table 12.

[0216] [Table 13]

[0217] Western blot analysis was used to detect α-syn protein levels. For this purpose, proteins were extracted using RIPA buffer and Tissue lyzer (Qiagen). Similar protein amounts from different treatment conditions were loaded onto SDS PAGE and Western blot was performed using anti-human α-syn antibody (Table 12) to detect α-syn levels. Tubulin was used for normalization and detected using anti-tubulin antibody (Table 13).

[0218] [Table 14]

[0219] result: In vitro experiments In vitro silencing efficacy of artificial miSNCA constructs To evaluate the miSNCA knockdown potency of miSNCA constructs in vitro, HEK293T cells were co-transfected with Renilla luciferase reporter encoding the SNCA gene. Firefly luciferase (FL) gene was expressed from the same reporter vector and used as an internal control to correct for transfection efficiency. In the initial screening, HEK cells were co-transfected with 1ng-10ng-50ng or 250ng of each miSNCA construct and Dual Luc reporter carrying the SNCA gene. Among the 17 miSNCA constructs designed to target the SNCA gene, miSNCA2, miSNCA5, miSNCA7, miSNCA12, miSNCA13, miSNCA15 and miSNCA16 induced a dose-dependent decrease in the RL / FL ratio. To further determine the potency, the above constructs were further used in titration experiments. The constructs were co-transfected into HEK293T cells with 10 ng of SNCA luciferase reporter plasmid at different concentrations: 0.1, 1, 10 or 100 ng. According to these results, transfection with 100 ng of miSNCA plasmid showed at least 50% reduction for all miSNCA candidates used in the titration experiment (Figure 3). miSNCA5, miSNCA13 and miSNCA15 were selected for further testing in different models due to their relatively large potency in reducing mSNCA levels.

[0220] To improve the efficacy of miSNCA candidates, i.e., the natural companions of miR451, modified miR144 was added to the scaffolds of miSNCA5 and miSNCA15 (FIG. 2B) (SEQ ID NOs: 32-33). These constructs were designed such that modified miR144 was added to the scaffold at the 5' end of miR451 carrying the miSNCA candidates. Dual luciferase assays were performed to evaluate the efficacy of the original and improved miSNCA candidates. The constructs (miSNCA5 (SEQ ID NO: 25), miSNCA15 (SEQ ID NO: 29), miSNCA5+miR144 (SEQ ID NO: 31), miSNCA15+miR144 (SEQ ID NO: 32) and control miRNA were co-transfected into HEK293T cells with 10 ng of SNCA luciferase reporter plasmid at different amounts: 0.1, 1, 10 or 100 ng per 24-well. The results showed that the potency of miSNCA5 and miSNCA15 was improved by at least 2-3 fold (Figure 4).

[0221] Reduction of endogenous SNCA expression in transfected cells The miSNCA5, miSNCA13 and miSNCA15 constructs were selected to test knockdown of SNCA mRNA expression in cells. Knockdown of endogenous SNCA gene expression in HEK293T cells was confirmed by RT-QPCR on transfected cells. Transfection of 50ng-200ng-1000ng of miRNA plasmids resulted in a reduction of SNCA mRNA expression by less than 40% by all miSNCA candidates tested. The results were consistent at the protein level with a dose-dependent reduction in α-syn levels measured by HTRF (Figure 5).

[0222] miRNA expression levels in transduced cells (small RNA sequencing data) The expression levels of mature miRNAs were quantified based on the number of total reads annotated by using miRBase and the pre-miRNA sequences of interest. 6The expression levels of the top 30 and 35 most expressed miRNAs in DA neurons transduced with HEK-produced AAV5-miSNCA at an MOI of 1 / cell were obtained (Figures 6A and 6B), and the expression levels of miSNCA5 (Figure 6A) and miSNCA15 (Figure 6B) were well within the range of endogenous miRNA levels.

[0223] Processing of miSNCA constructs upon transfection in cells (NGS data) miRNA processing was also examined by alignment of reads to pre-miRNA sequences: for miSNCA5 the length of the most abundant form was 24 nt, followed by 23 nt and 25 nt (Figure 7A); for miSNCA15 it was 22 nt, followed by 24 nt and 23 nt (Figure 7B).

[0224] AAV5-miSNCA transduction in human cells To examine the ability of AAV5-miSNCA5 and AAV5-miSNCA15 to transduce and deliver the packaged expression cassettes, DA neurons or forebrain neurons and / or LUHMES-derived DA neurons were infected with AAV5-miSNCA5 and AAV5-miSNCA15 at various multiplicities of infection (MOI); 4 , 10 5 , 10 6 and 10 7 Transduce cells with 100% ribosomal RNA (100% ribosomal RNA). Measure vector DNA levels and there should be a dose-dependent increase in vDNA levels in these cells. Isolate RNA from the transduced cells and measure SNCA mRNA levels using a RT-qPCR Syber Green assay. Expect a dose-dependent mRNA decrease in SNCA levels in these transduced cells.

[0225] Processing of miSNCA constructs from baculovirus-produced constructs (NGS data) Processing of miRNA extracted from rat brain tissue from in vivo study #2, group #4 was also investigated to evaluate the processing of baculovirus-produced AAV5-miSNCA. Small RNA sequencing was performed on these samples, and the data were aligned with the reads to the pre-miRNA sequence. The length of the most abundant form for miSNCA5 was 23 nt, followed by 24 nt and 25 nt; for miSNCA15, it was 22 nt, followed by 24 nt and 23 nt (Figure 12).

[0226] In vivo testing Study 1. Different administration routes of AAV5-GFP in WT rats showed good coverage in the target area affected by Parkinson's disease. To address the suitability of AAV5 vectors for delivering miSNCA candidates to target brain regions, coverage of brain regions that show significant α-syn pathology in Parkinson's disease (brainstem, midbrain, cortex) was evaluated after AAV5 administration. Different administration routes were tested: substantia nigra (SN), striatum or cisterna magna. GFP was used as a reporter gene. AAV5-GFP injected in the SN, at the two doses tested, or in the striatum, at the single dose tested, showed adequate biodistribution in the target regions, as assessed by AAV-GFP vDNA levels in the brain (Figure 9A) and corresponding GFP mRNA expression (Figure 9B). AAV5-GFP injected into the cisterna magna (directly into the cerebrospinal fluid) equally covered all brain regions examined, although to a lesser extent. It was therefore concluded that AAV5 is a suitable vector to deliver miSNCA candidates to brain regions of interest for Parkinson's disease treatment.

[0227] Study 2. AAV5-miSNCA candidate reduced human SNCA mRNA expression in a-syn KI rats To evaluate the ability of two design candidates (miSNCA5 and miSNCA15) in reducing human SNCA mRNA expression, AAV5-miSCR (non-targeting scrambled control), AAV5-miSNCA5 or AAV5-miSNCA15 were injected into the left striatum of adult a-syn KI rats. One group was injected with an equivalent dose of AAV5-miSNCA5 combined with AAV5-miSNCA15. miSNCA13 was excluded from the in vivo study because it targets an area outside the humanized portion of the SNCA KI rat model and has three mismatches to the WT rat SNCA gene. The right striatum was injected with formulation buffer and used as an additional control. At the single dose used, vDNA was detected in the AAV5-injected brain hemisphere, whereas in the control hemisphere, vDNA levels were below the lower limit of quantification (LLOQ) (Figure 10-1A). Transduction resulted in the expression of miSNCA candidates 5 and 15 or a combination of both in a vector-specific manner (Figure 10-1B and Figure 10-2C): miSNCA5 was detected only in the AAV5-miSNCA5-injected hemisphere, miSNCA15 was detected only in the AAV5-miSNCA15-injected hemisphere, and miSNCA5 and miSCNA 15 were detected in the AAV5-miSNCA5+AAV5 miSNCA15-injected group. At the single dose used, AAV5-miSNCA5 and AAV5-miSNCA5+AAV5-miSNCA15 were effective in reducing SNCA mRNA expression in the injected striatum as assessed by two different RT-QPCR SNCA assays (primer set SNCA1 and primer set SNCA 2) compared to the control striatum (Figure 10-2D). This study supports the mechanism of action of the AAV5-miSNCA candidate to reduce human SNCA mRNA expression and α-syn toxicity for the treatment of Parkinson's disease.

[0228] Study 3. Study in the AAV-Syn Rat Model Different AAV5-miSNCA candidates were tested in the AAV-Syn rat model.

[0229] To demonstrate the in vivo proof of concept of reducing SNCA levels and thereby improving the motor phenotype of human A53T mutant of α-syn virus overexpression, a rat PD model was used (AAV1 / 2-Ha53T-aSyn). Unilateral injections of both AAV1 / 2-hSNCA and AAV5-miSNCA viruses were performed in the right substantia nigra (SN). In both the simultaneous and sequential injection groups, vDNA was detected in the AAV5-injected hemisphere in the striatum at the single dose used (Figure 13), and in the control hemisphere (left striatum), vDNA levels were below the lower limit of quantification (LLOQ) (not shown). Transduction resulted in expression of miSNCA5 and miSNCA15 in a vector-specific manner (FIG. 14A and B): miSNCA5 was detected only in the AAV5-miSNCA5-injected hemisphere, and miSNCA15 was detected only in the AAV5-miSNCA15-injected hemisphere, and neither was detected in other samples from the negative control group. In A 53 T-aSyn animals, AAV5-miSNCA5 and AAV5-miSNCA15 were effective in reducing SNCA mRNA expression in the striatum at the injection site, as assessed by Taqman RT-qPCR assay (SNCA 2 primer and probe combination), compared to control striatum injected with an unrelated miRNA (solid black line) (FIG. 15), at the single dose used. miSNCA expression also showed a reduction at the protein level, reflected by reduced α-syn protein levels measured by ELISA (FIG. 16). Dopamine transporter deficiency measured by [125I]-RTI-121 autoradiography was evident in A53T-aSyn animals continuously injected with control miRNA (irrelevant miR, group 6 in Table 10), as in PD patients, and was corrected in miSNCA-treated groups (groups 7 and 8 in Table 10) (Figure 17). Correction of Ha53T-aSyn-induced striatal dopamine deficiency by miSNCA candidates was observed in association with metabolite changes in this model. Figure 18A shows dopamine levels in the test groups, and Figure 18B shows (DOPAC+HVA) / DA levels measured by LC / MS.

[0230] Motor behavior, as measured by the percentage asymmetry of left paw use, was significantly improved in the sequential injection groups receiving miSNCA5 or miSNCA15 treatment on day 56 compared to baseline levels (Figures 19A and 19B).

[0231] The molecular, biochemical and motor behavioral results were supported by histological observations. Immunostaining and quantification of dopaminergic (TH positive) and α-syn positive neurons in the substantia nigra showed that both AAV5-miSNCA candidates (continuous injection group) rescued dopaminergic (TH) neuronal cell loss (Figure 20-1A) and reduced human α-syn cell numbers (Figure 20-1B). This was reflected by a reduction in the percentage of positive dopaminergic (TH) cells that expressed α-syn (Figure 20-2C). A reduction in inflammation in this model, as assessed by Iba1 immunoreactivity in the substantia nigra, is also expected.

[0232] Overall, AAV5-miSNCA reversed the disease phenotype, improved the motor phenotype, and rescued molecular and neurochemical changes in the AAV-Syn rat model, demonstrating that miSNCA treatment is an effective therapy for reducing α-syn toxicity.

[0233] Test 4. Phenotypic rescue in a C. elegans PD model using miSNCA candidate sequences To compare the movement speed between worms fed by different plasmid-expressing E. coli, 100 C. elegans per condition were video tracked. Results showed that worms fed by full-length SNCA-expressing or miSNCA-expressing E. coli showed improved movement speed compared to worms fed by E. coli transformed with an empty plasmid (Figure 11). Worms treated with full-length SNCA or miSNCA showed increased speed compared to untreated worms on all days their movement was tracked. These results indicate that decreasing the expression of the SNCA gene, and thereby reducing α-syn levels, improves the movement phenotype in this C. elegans PD model. Furthermore, the results demonstrate that treatment of worms at different life stages is possible.

[0234] Treatment with miSNCA reduced SNCA mRNA levels (Figures 21-1A-21-1C) and α-synuclein protein levels (Figures 21-2D-21-2F) in a C. elegans PD model when they were treated at the larval or adult stages. Consistent with this, miSNCA treatment rescued the locomotor phenotypic behavior in this model, as shown in Figure 22 as improved swimming speed in miSNCA-treated worms compared to negative control worms (EV-treated worms).

[0235] Small RNA sequencing performed on C. elegans samples collected from worms treated with miSNCA5, miSNCA15, and full-length SNCA demonstrates the presence of correctly processed miSNCA candidates in the samples (Figures 23-1 and 23-2). miSNCA5 and miSNCA15 sequences, as well as other miSNCA sequences (e.g., miSNCA 7, miSNCA12, and miSNCA13), were detected in the full-length SNCA treated sample.

Claims

**Claim 1** A nucleic acid comprising a nucleic acid sequence encoding RNA, wherein the RNA sequence contained in the RNA is substantially complementary to a target sequence of the α-synuclein (α-syn) gene (SNCA), the RNA sequence has at least 15 nucleotides, the RNA contains a hairpin, and the RNA contains SEQ ID NO: 1, SEQ ID NO: 2, or a variant of SEQ ID NO: 1 or SEQ ID NO:

2. **Claim 2** The nucleic acid according to claim 1, wherein the hairpin contains at least 39 nucleotides. **Claim 3** The nucleic acid according to claim 1, wherein the RNA sequence has at least 18 nucleotides. **Claim 4** The nucleic acid according to claim 1, wherein the RNA sequence has a maximum of 32 nucleotides. **Claim 5** The nucleic acid according to claim 1, wherein the target sequence is a part of an exon contained in the α-syn gene. **Claim 6** The nucleic acid according to claim 5, wherein the exon is selected from the group consisting of exon 2, exon 4, and exon 6. **Claim 7** The nucleic acid according to claim 5, wherein the part of the exon consists of a sequence selected from the group consisting of SEQ ID NOs: 3-9 and variants of SEQ ID NOs: 3-9. **Claim 8** The nucleic acid according to claim 1, wherein the RNA sequence contains one sequence selected from the group consisting of SEQ ID NOs: 10-16 and variants of SEQ ID NOs: 10-16. **Claim 9** The nucleic acid according to claim 1, which is a DNA molecule. **Claim 10** A DNA molecule contained in a DNA expression cassette, wherein in the DNA expression cassette, a promoter and a poly A tail are further included, and the nucleic acid is adjacent to an inverted terminal repeat sequence (ITR). **Claim 11** The DNA molecule according to claim 10, wherein the promoter is a ubiquitous promoter; a neuron-specific promoter; or a glia-specific promoter. **Claim 12** An adeno-associated virus (AAV) vehicle comprising the DNA molecule according to claim 9. **Claim 13** The AAV vehicle according to claim 12, comprising a capsid containing an AAV5 or AAV9 capsid protein sequence. **Claim 14** The AAV vehicle according to claim 12, wherein the AAV vehicle is a gene therapy vehicle. **Claim 15** A composition comprising the AAV vehicle according to claim 14 and at least one pharmaceutically acceptable excipient. **Claim 16** The AAV vehicle according to claim 12 for use as a medicament.

17. The composition according to claim 15 for use as a medicament.

18. The AAV vehicle according to claim 16, wherein the medicament reduces and / or knocks down transcripts encoded by the α-syn gene.

19. The composition according to claim 17, wherein the medicament reduces and / or knocks down transcripts encoded by the α-syn gene.

20. The AAV vehicle according to claim 16, wherein the medicament reduces the amount of Lewy bodies and / or Papp-Lantos bodies.

21. The composition according to claim 17, wherein the medicament reduces the amount of Lewy bodies and / or Papp-Lantos bodies.

22. The AAV vehicle according to claim 16, wherein the medicament is used to treat and / or prevent clinical symptoms of Parkinson's disease (PD), Lewy body dementia (LBD), multiple system atrophy (MSA), neuropathy symptoms, motor symptoms of PD, cognitive impairment, sleep disorder, autonomic neuropathy, and / or olfactory disorder.

23. The composition according to claim 17, wherein the medicament is used to treat and / or prevent clinical symptoms of Parkinson's disease (PD), Lewy body dementia (LBD), multiple system atrophy (MSA), neuropathy symptoms, motor symptoms of PD, cognitive impairment, sleep disorder, autonomic neuropathy, and / or olfactory disorder.

24. The AAV vehicle according to claim 16, wherein the medicament is used to treat and / or prevent PD and / or MSA.

25. The composition according to claim 17, wherein the medicament is used to treat and / or prevent PD and / or MSA.

26. A method for manufacturing the AAV vehicle according to claim 12.

27. A kit comprising the AAV vehicle according to claim 12, further comprising an immunosuppressive compound.

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