Methods and compositions for non-viral DNA delivery

Abstract

The present invention features methods and compositions that can be used to facilitate intracellular delivery of DNA to a subject. The methods and compositions provided use nanoparticles for intracellular DNA delivery and cytoplasmic DNA sensing inhibitors. The cytoplasmic DNA sensing inhibitors are provided to reduce immune responses stimulated by DNA in a subject.

Description

[Technical field]

[0001] The present invention relates to the field of intracellular non-viral DNA delivery to a subject. The methods and compositions provided have a variety of applications, including gene therapy. REFERENCE TO ELECTRONICALLY SUBMITTED SEQUENCE LISTING

[0002] The contents of the electronic sequence listing (SequenceListing_9WO1.xml; Size: 3,810 bytes, Created: July 14, 2022) are incorporated herein by reference in their entirety. [Background technology]

[0003] Gene therapy uses nucleic acids to modify a subject's DNA to achieve a beneficial effect. Genetic modification can be achieved using a variety of strategies, including gene enhancement, gene suppression, and genome editing. (Anguela and High Annu. Rev. Med. 2019,70,73;and Li et al.,Signal Transduction and Targeted Therapy 2020,5,1.)

[0004] An effective delivery system for nucleic acids is important for the success of gene therapy. Successful delivery of nucleic acids provides target cells with sufficient quantities to have a beneficial effect without producing unacceptable side effects. The delivery system must protect the genetic material from enzymatic degradation, have a sufficiently long life span in the body, be able to reach the required site in the body, have an acceptable toxicity, and be able to cross cell membranes.

[0005] Gene therapy vectors are broadly classified as viral and non-viral. Each vector has its advantages and disadvantages. Viral vectors are generally more efficient at delivering genetic material to cells, but have a higher potential for immunogenicity, toxin production, and insertional mutagenesis, as well as a limited capacity for gene transfer. Advantages of non-viral vectors include a larger transgene capacity, the ability to be administered to subjects who already have antibodies against the vector capsid, and the ability to re-administer to subjects. Challenges associated with non-viral delivery include lower transfection efficiency, potential for nucleic acid degradation, innate immunity, lower efficiency of gene delivery to somatic cell targets, and lower levels of gene expression in vivo compared to viral approaches. (Hardee et al.,Genes 2017,8,65 and Nayerossadat et al.,Adv.Biomed Res.2012,1,27.) Summary of the Invention [Problem to be solved by the invention]

[0006] The present invention features methods and compositions that can be used to facilitate intracellular delivery of DNA to a subject. The methods and compositions provided use nanoparticles for intracellular DNA delivery and cytoplasmic DNA sensing inhibitors. The cytoplasmic DNA sensing inhibitors are provided to reduce immune responses stimulated by DNA in a subject.

[0007] Thus, a first aspect of the invention describes a method for intracellular delivery of DNA comprising administering to a subject: a) a cytoplasmic DNA sensing inhibitor selected from the group consisting of a cyclic GMP-AMP synthase-stimulator of interferon genes (cGAS-STING) pathway inhibitor and an inflammasome pathway inhibitor; and b) Nanoparticles containing DNA.

[0008] Another embodiment of the present invention describes a nanoparticle comprising (a) DNA and (b) a cytoplasmic DNA-sensing inhibitor selected from the group consisting of a cGAS-STING pathway inhibitor and an inflammasome pathway inhibitor.

[0009] Further aspects of the present invention include pharmaceutical compositions comprising the nanoparticles described herein, pharmaceutical compositions for use as described herein, and preparations of medicaments for use as described herein.The pharmaceutical compositions for use as described herein can provide a DNA vector comprising a transgene for use in a patient, which is administered before, simultaneously, or after a cytoplasmic DNA sensing inhibitor.Similarly, preparations of medicaments for use as described herein can include preparations of pharmaceutical compositions comprising a DNA vector comprising a transgene for use in a patient, which is administered before, simultaneously, or after a cytoplasmic DNA sensing inhibitor.

[0010] Other features and advantages of the present invention will be apparent from the additional description provided herein, including the various examples. The examples provided illustrate various components and methodologies useful in practicing the invention. Such examples do not limit the claimed invention. Based on this disclosure, one of ordinary skill in the art will be able to identify and employ other components and methodologies useful in practicing the invention. [Brief description of the drawings]

[0011] [Figure 1] Figure 1 shows the results of an in vitro test using cultured cells on the ability of a small molecule STING inhibitor (H-151) to inhibit DNA-LNP-induced interferon regulatory factor (IRF) activation. Two different amounts of H-151 (0.2 ng and 2.1 ng) were used. The white bar graph on the left shows cells treated with DNA-LNP without the H-151 inhibitor (0). When H-151 was added (0.2 and 2.1), the white boxes indicate that H-151 is soluble, and the gray boxes indicate that H-151 is encapsulated in the DNA-LNP (LNP encapsulation).

[0012] [Diagram 2]Figures 2A, 2B, 2C, and 2D show the results of in vivo studies on the ability of H-151 encapsulated in DNA-LNPs to inhibit DNA-LNP-induced IFN-β (Figure 2A), IFN-α (Figure 2B), IFN-γ (Figure 2C), and IL-6 (Figure 2D).

[0013] [Diagram 3] Figures 3A, 3B, 3C, 3D, 3E, 3F, 3G, and 3H show the results of in vivo studies on the ability of RO3150, GSK690693, and dexamethasone to inhibit DNA-LNP-induced cytokine / chemokine levels.

[0014] [Figure 4] Figures 4A, 4B, 4C, 4D, and 4E show the effect of STING signal blockade on DNA-LNP tolerability and transgene expression in mice administered DNA-LNP gene therapy. Inflammatory responses to DNA-LNP were assessed in wild-type mice (WT) with functional STING and mice carrying a Goldentiquet missense mutation in the cytoplasmic double-stranded DNA (dsDNA) sensor (STING(Gt)). Baseline cytokine levels were measured from pooled plasma samples of WT mice not administered DNA-LNP (baseline). In mice administered DNA-LNP, STING(Gt) mice had reduced plasma IL-6 levels (Figure 4A), reduced plasma IFNα (Figure 4B), reduced plasma IFN-γ (Figure 4C), extended survival (Figure 4D), and increased transgene expression (Figure 4E) compared to WT mice. ULOQ indicates upper limit of quantification. LLOQ indicates lower limit of quantification. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0015] The present invention features a method and composition for intracellular DNA delivery to a subject using nanoparticles containing DNA and a cytoplasmic DNA sensing inhibitor selected from the group consisting of cGAS-STING pathway inhibitors and inflammasome pathway inhibitors.Intracellular DNA delivery has various applications, such as the delivery of DNA vectors to a subject to express transgenes.The advantage of inhibiting cGAS-STING pathway and / or inflammasome pathway may be reduced susceptibility to inflammatory responses caused by DNA payloads.

[0016] "Nanoparticles" refers to small non-viral particles that can encapsulate or bind DNA, facilitating DNA delivery to cells. Nanoparticles can also be used to deliver, for example, different DNA vectors, different transgenes, cytoplasmic DNA sensing inhibitors, immune cell modulators. The size of nanoparticles ranges from about 10 nm to about 1000 nm. In different embodiments, the nanoparticles are about 50 nm to about 500 nm, or about 50 nm to about 200 nm.

[0017] "Subject" refers to mammals, including humans, non-human primates such as apes, gibbons, gorillas, chimpanzees, orangutans, macaques, domestic animals such as dogs and cats, livestock such as poultry, ducks, horses, cows, goats, sheep, pigs, and laboratory animals such as mice, rats, rabbits, and guinea pigs. Preferred subjects are human subjects to be treated. However, subjects also include animal disease models, e.g., mouse and other animal models of protein / enzyme deficiencies such as Pompe disease (GAA deficiency), glycogen storage disease (GSD), etc.

[0018] A "DNA vector" is a DNA sequence containing a transgene linked to regulatory elements for expressing RNA from the transgene. The RNA produced may be functional by itself or may code for a protein. One type of regulatory element is a promoter, which binds RNA polymerase and necessary transcription factors to initiate transcription. If coding for a protein, the produced RNA sequence also codes for a termination sequence at the end of the coding sequence. Other regulatory elements include those that affect RNA expression, RNA stability, and protein production. DNA vectors may be single-stranded, double-stranded, or a combination of single- and double-stranded. A DNA vector may also contain multiple transgenes and multiple regulatory elements of the same or different types.

[0019] The term "operably linked" refers to the association of two or more nucleic acid segments in a single nucleic acid so that the function of one is affected by the other.

[0020] "Transgene" refers to a region of DNA capable of being expressed into RNA, regardless of the origin of the polynucleotide sequence. A transgene is generally a portion of a larger nucleic acid that contains at least one region with which the transgene is not normally associated in nature.

[0021] A cytoplasmic DNA sensing inhibitor selected "from the group consisting of" provides that at least one member of the group is present, and does not exclude, for example, the presence of both members of the group or the presence of one or more additional inhibitors.

[0022] A first aspect of the invention describes a method for intracellular delivery of DNA to a subject comprising administering: a) a cytoplasmic DNA sensing inhibitor selected from the group consisting of a cGAS-STING pathway inhibitor and an inflammasome pathway inhibitor; and b) first nanoparticles comprising DNA; wherein step (b) is carried out prior to, simultaneously with, or after step (a).

[0023] A second aspect of the invention describes a method for intracellular delivery of DNA to a subject comprising administering: a) a cytoplasmic DNA sensing inhibitor selected from the group consisting of a cGAS-STING pathway inhibitor and an inflammasome pathway inhibitor; and b) a first nanoparticle comprising DNA; with the proviso that, when the first nanoparticle is a lipid nanoparticle, at least one of the following: (i) the cytoplasmic DNA sensing inhibitor is at least an inflammasome pathway inhibitor; (ii) the lipid nanoparticle does not contain an endosomolytic agent; (iii) the DNA is circular; (iv) the DNA is not closed-ended DNA; or (v) the cytoplasmic DNA sensing inhibitor is provided in a second nanoparticle, wherein the second nanoparticle can have the same or a different composition as the first nanoparticle; and wherein step (b) is performed prior to, simultaneously with, or after step (a).

[0024] Stanton and Manganiello, International Patent Publication No. WO2020 / 181168, refer to the use of various endosomolytic agents and LNPs that contain endosomolytic agents and closed DNA.

[0025] In a first embodiment of the first and second aspects, the DNA is a DNA vector comprising a transgene operably linked to a regulatory element. In a further embodiment, the transgene is operably linked to a promoter; operably linked to a promoter / enhancer; operably linked to a promoter / enhancer, polyadenylation and termination signals, and / or regulatable elements; and the DNA vector comprises from 5' to 3' the promoter / enhancer, the transgene, and polyadenylation and termination signals.

[0026] References to 5' to 3' with respect to particular elements indicate the relative positions of the different elements and do not require that the different elements be contiguous to one another, and allow for the presence of additional sequences. Additional sequences that provide additional activity can be located in different positions, such as between the two identified elements, at the 3' end, at the 5' end, etc.

[0027] In a second embodiment of the first and second aspects, the DNA sensing inhibitor is a cGAS-STING pathway inhibitor; and the DNA is as provided in the first or second aspect, or first embodiment. In a further embodiment, the cGAS-STING pathway inhibitor is a cGAS inhibitor; the cGAS-STING pathway inhibitor is a STING inhibitor; the cGAS-STING pathway inhibitor is a TBK1 inhibitor; the cGAS-STING pathway inhibitor is a cGAS inhibitor as provided in Section II.A., infra; the cGAS-STING pathway inhibitor is a STING inhibitor as provided in Section II.A., infra; and / or the cGAS-STING pathway inhibitor is a TBK1 inhibitor as provided in Section II.A., infra. In further embodiments, the inhibitor is H-151, GSK-690693, RU-521, RO-3150, ISD 017, SI-001, CYT387 or GSK8612, or a pharma- ceutically acceptable salt thereof; or a compound of Table 1, Table 2 or Table 3, or a pharma- ceutically acceptable salt thereof.

[0028] Reference to a particular embodiment includes reference to further embodiments provided therein. For example, a reference to a first embodiment in a second embodiment provides a reference to all embodiments provided in the first embodiment, including further embodiments provided therein.

[0029] In a third embodiment of the first and second aspects, the cytoplasmic DNA sensing inhibitor is an inflammasome pathway inhibitor, and the DNA is as provided in the first or second aspect, or the first embodiment. In a further embodiment, the inflammasome pathway inhibitor is an AIM2 inhibitor; the AIM2 inhibitor is as provided in Section II.B, infra, and the AIM2 inhibitor is A151.

[0030] In a fourth embodiment of the first and second aspects, the DNA is a DNA vector comprising a transgene encoding a viral antigen, a bacterial antigen, a therapeutic protein, a short hairpin RNA (shRNA), a small interfering RNA (siRNA), a microRNA (miRNA), an RNA i , a DNA vector comprising a ribozyme, an antisense RNA, a CRISPR (clustered regularly interspaced short palindromic repeats) / Cas9 construct, a zinc finger nuclease (ZFN), or a transcription activator-like effector nuclease (TALEN); wherein the DNA is as provided in the first embodiment; and the cytoplasmic DNA-sensing inhibitor is as provided in the first or second aspect, the second embodiment, or the third embodiment. In a further embodiment, the therapeutic protein is as provided in Section III.D., infra.

[0031] In a fifth embodiment, the DNA provided in any of the first or second aspects or related embodiments is circular DNA. Reference to "related embodiments" refers to each provided embodiment (including further embodiments) that is referenced in relation to a particular aspect.

[0032] In a sixth embodiment of the first and second aspects, the cytoplasmic DNA sensing inhibitor is provided in a second nanoparticle; the DNA is as provided in the first or second aspect or the first, fourth or fifth embodiment; and the cytoplasmic DNA sensing inhibitor is as provided in the first or second aspect, the second embodiment or the third embodiment. In a further embodiment, the second nanoparticle has substantially the same composition as the first nanoparticle; and the first and second nanoparticles are lipid nanoparticles or lipid-polymer nanoparticles.

[0033] In a seventh embodiment of the first and second aspects, the cytoplasmic DNA sensing inhibitor is provided together with DNA in the first nanoparticle; the DNA is as provided in the first or second aspect, or the first, fourth or fifth embodiment; and the cytoplasmic DNA sensing inhibitor is as provided in the first or second aspect, the second embodiment or the third embodiment. In further embodiments, the first nanoparticle is a lipid nanoparticle; the first nanoparticle is a lipid polymer nanoparticle; the first nanoparticle is an exosome; the first nanoparticle is configured to release the inhibitor prior to release of the DNA; the first nanoparticle is a lipid nanoparticle configured to release the inhibitor prior to release of the DNA; the first nanoparticle is a lipid polymer nanoparticle configured to release the inhibitor prior to release of the DNA; and the first nanoparticle is an exosome configured to release the inhibitor prior to release of the DNA.

[0034] In the eighth embodiment of the first and second aspects, and in related embodiments, the cytoplasmic DNA sensing inhibitor is administered at about the same time, before or after DNA administration.In different embodiments, the cytoplasmic DNA sensing inhibitor is administered at least 30 minutes, at least 60 minutes, at least 90 minutes, or at least 120 minutes before DNA administration; the cytoplasmic DNA sensing inhibitor is administered at about the same time, up to about 5 minutes, up to about 15 minutes, up to about 30 minutes, up to about 45 minutes, up to about 60 minutes, up to about 90 minutes, up to about 2 hours, up to about 3 hours, up to about 4 hours, up to about 5 hours, up to about 6 hours, up to about 7 hours, up to about 8 hours, up to about 9 hours, up to about 10 hours, up to about 12 hours, up to about 1 day, up to about 2 days, up to about 3 days, up to about 4 days, or up to about 1 week before DNA administration. Preferably, the cytoplasmic DNA sensing inhibitor is administered at about the same time as the DNA vector administration, up to about 5 minutes, up to about 15 minutes, up to about 30 minutes, up to about 45 minutes, up to about 60 minutes, up to about 90 minutes, up to about 2 hours, up to about 3 hours, or up to about 4 hours before the DNA vector administration. In different embodiments, the cytoplasmic DNA sensing inhibitor is administered at least 15 minutes, at least 30 minutes, at least 45 minutes, at least 60 minutes, at least 90 minutes, at least 120 minutes, or at least one day after the DNA vector administration.

[0035] In a ninth embodiment of the first and second aspects, two different cytoplasmic DNA sensing inhibitors are used; wherein other components and administration are as provided in the first aspect, the second aspect, or related embodiments. The different inhibitors can be provided without nanoparticles, in different nanoparticles, or in the same nanoparticles. In further embodiments, an inflammasome pathway inhibitor and a cGAS-STING pathway inhibitor are administered; two different inflammasome pathway inhibitors are administered; and two different cGAS-STING pathway inhibitors are administered.

[0036] In a tenth embodiment of the first and second aspects or related embodiments, the subject is a human patient.

[0037] In an eleventh embodiment of the first and second aspects or related embodiments, the DNA and DNA vectors comprise substantially double-stranded DNA, or the DNA and DNA vectors comprise substantially single-stranded DNA. The DNA includes double-stranded DNA, single-stranded DNA, and DNA having single-stranded and double-stranded regions. With respect to DNA, including DNA constituting a vector, "substantially" comprises or is composed of double-stranded DNA means that more than half, at least 75%, at least 90%, at least 95%, or at least 99% of the DNA is double-stranded DNA, or 100% of the DNA is double-stranded DNA. With respect to DNA, including DNA constituting a vector, "substantially" comprises or is composed of single-stranded DNA means that more than half, at least 75%, at least 90%, at least 95%, or at least 99% of the DNA is single-stranded DNA, or 100% of the DNA is single-stranded DNA.

[0038] In a twelfth embodiment of the first and second aspects or related embodiments, the nanoparticles are LNPs. In a further embodiment, the LPNs (mol%) comprise, consist essentially of, or consist of the following components: (1) about 20% to about 65% of one or more cationic lipids, about 1% to about 50% of one or more phospholipids, about 0.1% to 10% of one or more PEGylated lipids, and about 0% to about 70% of cholesterol; and (2) about 20% to about 50% of one or more cationic lipids, about 5% to about 20% of one or more phospholipids, about 0.1% to about 5% of one or more PEGylated lipids, and about 20% to about 60% of cholesterol. In a further embodiment, the lipid of the phospholipid is a neutral lipid; and the lipid of the phospholipid is DOPE or DSPC.

[0039] In a thirteenth embodiment or related embodiments of the first and second aspects, the LNP (mol %) comprises, consists essentially of, or consists of the following components: (1) cKK-E12 (further described in IA below), about 35%; C14-PEG2000, about 2.5%; cholesterol, about 46.5%; and DOPE, about 16%; (2) bCKK-E12 (further described in IA below), about 35%; C14-PEG2000, about 2.5%; cholesterol, about 46.5%; and DOPE, about 16%; (3) Lipid9 (described further in Sabnis et al., and in the IA, infra), about 50%; C14-PEG2000, about 1.5%; cholesterol, about 38.5%; and DSPC, about 10%; or (4) Lipid5 (described further in Sabnis et al., and in the IA, infra), about 50%; C14-PEG2000, about 1.5%; cholesterol, about 38.5%; and DSPC, about 10%; and (5) ionizable lipid, about 50%; DSPC, about 10%; cholesterol, about 37.5%; and stabilizer (PEG-lipid), about 2.5%; or (6) GenVoy-ILM TM LNP (Precision NanoSystems).

[0040] A third aspect of the invention features a nanoparticle composition that includes: a) DNA, and b) A cytoplasmic DNA sensing inhibitor selected from the group consisting of a GAS-STING pathway inhibitor and an inflammasome pathway inhibitor.

[0041] A fourth aspect of the invention features a nanoparticle comprising: a) DNA, and b) a cytoplasmic DNA sensing inhibitor selected from the group consisting of a cGAS-STING pathway inhibitor and an inflammasome pathway inhibitor; with the proviso that, when the nanoparticle is a lipid nanoparticle, at least one of the following: (i) the cytoplasmic DNA sensing inhibitor is at least an inflammasome pathway inhibitor; (ii) the lipid nanoparticle does not contain an endosomolytic agent; (iii) the DNA is circular; (iv) the DNA is not closed DNA; or (v) the cytoplasmic DNA sensing inhibitor is provided in a second nanoparticle, which can have the same or different composition as the first nanoparticle.

[0042] In a first embodiment of the third and fourth aspects, the DNA is a DNA vector comprising a transgene, the transgene comprising a promoter operably linked to a regulatory element. In a further embodiment, the transgene is operably linked to a promoter; operably linked to a promoter enhancer; operably linked to a promoter / enhancer, polyadenylation and termination signals and / or regulatable elements; and the DNA vector comprises from 5' to 3' the promoter / enhancer, the transgene, and polyadenylation and termination signals.

[0043] In a first embodiment of the third and fourth aspects, the DNA is a DNA vector comprising a transgene operably linked to a regulatory element. In a further embodiment, the transgene is operably linked to a promoter; operably linked to a promoter / enhancer; operably linked to a promoter / enhancer, polyadenylation and termination signals, and / or regulatable elements; and the DNA vector comprises from 5' to 3' the promoter / enhancer, the transgene, and polyadenylation and termination signals.

[0044] In a second embodiment of the third and fourth aspects, the cytoplasmic DNA sensing inhibitor is a cGAS-STING pathway inhibitor; and the DNA is as provided in the third or fourth aspect or the first embodiment. In a further embodiment, the cGAS-STING pathway inhibitor is a cGAS inhibitor; the cGAS-STING pathway inhibitor is a STING inhibitor; the cGAS-STING pathway inhibitor is a TBK1 inhibitor; the cGAS-STING pathway inhibitor is a cGAS inhibitor as provided in Section II.A., infra; the cGAS-STING pathway inhibitor is a STING inhibitor as provided in Section II.A., infra; and / or the cGAS-STING pathway inhibitor is a TBK1 inhibitor as provided in Section II.A., infra. In further embodiments, the inhibitor is H-151, GSK-690693, RU-521, RO-3150, ISD 017, SI-001, CYT387 or GSK8612, or a pharma- ceutically acceptable salt thereof; or a compound of Table 1, Table 2 or Table 3, or a pharma- ceutically acceptable salt thereof.

[0045] In a third embodiment of the third and fourth aspects, the inhibitor is an inflammasome pathway inhibitor; and the DNA is as provided in the third or fourth aspect or the first embodiment. In a further embodiment, the inflammasome pathway inhibitor is an AIM2 inhibitor; the AIM2 inhibitor is as provided in Section II.B, infra, and the AIM2 inhibitor is A151.

[0046] In a fourth embodiment of the third and fourth aspects, the DNA is a DNA vector comprising a transgene encoding a viral antigen, a bacterial antigen, a therapeutic protein, a short hairpin RNA (shRNA), a small interfering RNA (siRNA), a microRNA (miRNA), an RNA i, a DNA vector comprising a ribozyme, an antisense RNA, a CRISPR (clustered regularly interspaced short palindromic repeats) / Cas9 construct, a zinc finger nuclease (ZFN), or a transcription activator-like effector nuclease (TALEN); wherein the DNA vector is as provided in the first embodiment; and the cytoplasmic DNA-sensing inhibitor is as provided in the third or fourth aspect, the second embodiment or the third embodiment. In a further embodiment, the therapeutic protein is as provided in Section III.D., infra.

[0047] In a fifth embodiment, the DNA is circular DNA as provided in the third or fourth aspect, or any of the related embodiments.

[0048] In a sixth embodiment of the third and fourth aspects, the nanoparticle is a lipid nanoparticle, a lipid-polymer nanoparticle, or an exosome; the DNA is as provided in the third or fourth aspect, or the first, fourth or fifth embodiment; and the cytoplasmic DNA-sensing inhibitor is as provided in the third or fourth aspect, or the second or third embodiment. In further embodiments, the nanoparticle is a lipid nanoparticle; the nanoparticle is a lipid-polymer nanoparticle; the nanoparticle is an exosome; the nanoparticle is a lipid nanoparticle configured to release the inhibitor prior to release of the DNA; the nanoparticle is a lipid-polymer nanoparticle configured to release the inhibitor prior to release of the DNA; the nanoparticle is an exosome configured to release the inhibitor prior to release of the DNA.

[0049] In a further embodiment, the nanoparticle is a LNP. In a further embodiment, the LPN (mol%) comprises, consists essentially of, or consists of the following components: (1) about 20% to about 65% of one or more cationic lipids, about 1% to about 50% of one or more phospholipids, about 0.1% to 10% of one or more PEGylated lipids, and about 0% to about 70% of cholesterol; and (2) about 20% to about 50% of one or more cationic lipids, about 5% to about 20% of one or more phospholipids, about 0.1% to about 5% of one or more PEGylated lipids, and about 20% to about 60% of cholesterol. In a further embodiment, the lipid of the phospholipid is a neutral lipid; and the lipid of the phospholipid is DOPE or DSPC.

[0050] In further embodiments, the LPN (mol %) comprises, consists essentially of, or consists of the following components: (1) cKK-E12 (further described in IA below), about 35%; C14-PEG2000, about 2.5%; cholesterol, about 46.5%; and DOPE, about 16%; (2) bCKK-E12 (further described in IA below), about 35%; C14-PEG2000, about 2.5%; cholesterol, about 46.5%; and DOPE, about 16%; (3) Lipid9 (described further in Sabnis et al., and in the IA, infra), about 50%; C14-PEG2000, about 1.5%; cholesterol, about 38.5%; and DSPC, about 10%; or (4) Lipid5 (described further in Sabnis et al., and in the IA, infra), about 50%; C14-PEG2000, about 1.5%; cholesterol, about 38.5%; and DSPC, about 10%; and (5) ionizable lipid, about 50%; DSPC, about 10%; cholesterol, about 37.5%; and stabilizer (PEG-lipid), about 2.5%; or (6) GenVoy-ILM TM LNP (Precision NanoSystems).

[0051] In a seventh embodiment of the third and fourth aspects, two different cytoplasmic DNA sensing inhibitors are provided in the nanoparticle; wherein the other components are as provided in the third or fourth aspect or related embodiments. In a further embodiment, an inflammasome pathway inhibitor and a cGAS-STING pathway inhibitor are provided; two different inflammasome pathway inhibitors are provided; and two different cGAS-STING pathway inhibitors are provided.

[0052] In an eighth embodiment of the third and fourth aspects or related embodiments, the DNA and the DNA vector each comprise substantially double-stranded DNA; and the DNA and the DNA vector each comprise substantially single-stranded DNA.

[0053] A fifth aspect is directed to a pharmaceutical composition comprising the nanoparticle composition of the third or fourth aspect or related embodiments and a pharma- ceutically acceptable carrier.

[0054] A sixth aspect is directed to a pharmaceutical composition for use in gene therapy comprising a DNA vector comprising a transgene, the composition being for use before, simultaneously with or after administration of a cytoplasmic DNA sensing inhibitor, the DNA vector being provided within a nanoparticle. Additional embodiments are provided for the methods described in the first and second aspects and related embodiments; and the compositions described in the third and fourth aspects and related embodiments.

[0055] A seventh aspect of the invention is directed to a method of manufacturing a medicament for use in the first and second aspects and related embodiments. The medicament is manufactured by combining nanoparticles with a pharma- ceutical acceptable carrier, wherein the nanoparticles are as described in the first, second, third, fourth aspect or related embodiments.

[0056] The singular forms "a," "an," and "the" include plural referents unless the context clearly indicates otherwise.

[0057] As used herein, the conjunction "and / or" between multiple mentioned elements is understood to encompass both individual and combined alternatives. For example, when two elements are joined by "and / or", the first alternative refers to the applicability of the first alternative without the second alternative, the second alternative refers to the applicability of the second alternative without the first alternative, and the third alternative refers to the applicability of the first and second alternatives together. Any of the alternatives is understood to be within the meaning and thus to satisfy the requirements of the term "and / or". The simultaneous application of one or more alternatives is also understood to be included in the meaning of the term "and / or".

[0058] Additionally, unless the context requires otherwise, the words "or" and "and" are intended to have the same meaning as "and / or."

[0059] Terms such as "including," "for example," "example," or "such as" followed by different members or examples are open-ended descriptions in which the listed members or examples are exemplary and other members or examples may be provided or used.

[0060] The terms "polypeptide," "protein," and "peptide" can be used interchangeably to refer to amino acid sequences without regard to function. Polypeptides and peptides contain at least two amino acids, and proteins contain at least about 10 amino acids. The amino acids provided include naturally occurring amino acids and amino acids provided by cellular modification.

[0061] References to "comprise" and variations such as "comprises," "comprising," and the like, when used in reference to an element or group of elements, are open-ended and do not exclude additional unrecited elements or method steps. Terms such as "including," "containing," "characterized by," and the like are synonymous with "comprising." In different aspects and embodiments described herein, references to open-ended terms such as "comprising" can be replaced with the terms "consisting" or "consisting essentially of."

[0062] The term "consisting of" excludes any element, step, or ingredient not specified in the recited claim element, unless such element, step, or ingredient is relevant to the claimed invention.

[0063] The reference "consisting essentially of" limits the scope of the claim to those materials or steps specified and that do not materially affect the basic and novel characteristics of the claimed invention.

[0064] The term "about" refers to values ​​within 10% of the underlying parameter (i.e., plus or minus 10%). For example, "about 1:10" includes 1.1:10.1 or 0.9:9.9, and "about 5 hours" includes 4.5 hours or 5.5 hours. Prefixing a value string with "about" modifies each value by 10%.

[0065] All numerical values ​​or numerical ranges include integers within the range and fractions of integers within the numerical value or numerical range, unless the context clearly indicates otherwise. Thus, a reference to a reduction of 95% or more includes 95%, 96%, 97%, 98%, 99%, 100%, as well as 95.1%, 95.2%, 95.3%, 95.4%, 95.5%, etc., 96.1%, 96.2%, 96.3%, 96.4%, 96.5%, etc.; a reference to a numerical range such as "1 to 4" includes 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 100%, 100% and the like; "1-4" includes 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28 days, and a numerical range such as "0.01-10" includes 0.011, 0.012, 0.013, etc., as well as 9.5, 9.6, 9.7, 9.8, 9.9, 10, etc. For example, a dose of "0.01mg / kg-10mg / kg" of subject weight includes 0.011mg / kg, 0.012mg / kg, 0.013mg / kg, 0.014mg / kg, 0.015mg / kg, etc., as well as 9.5mg / kg, 9.6mg / kg, 9.7mg / kg, 9.8mg / kg, 9.9mg / kg, etc.

[0066] References to more (larger) or less integers include numbers greater or less than the referenced number, respectively. Thus, for example, the phrase 2 or more times includes 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, and the phrase "2 or more times" includes 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, or more times.

[0067] In the background and throughout this specification, various references, including articles and patent documents, are cited or described. Each of these references is incorporated herein by reference in its entirety. No publication is admitted to be prior art with respect to the invention disclosed or claimed. In some cases, the incorporation of a particular reference into this specification by reference is indicated, with the incorporation being emphasized.

[0068] The definitions provided herein, including this section and other sections of this application, apply throughout this application.

[0069] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention pertains.

[0070] This specification is divided into various sections and paragraphs, providing various embodiments. These separations should not be considered as separating the substance of one paragraph, section or embodiment from the substance of another paragraph, section or embodiment. The description provided has broad application and encompasses all combinations of the various sections, paragraphs, and sentences envisioned. The discussion of any embodiments is intended to be exemplary only, and is not intended to suggest that the scope of the disclosure, including the claims, is limited to these examples (unless otherwise specified in the claims).

[0071] Although particular feature combinations are emphasized herein, all features disclosed herein can be combined in any combination. Each feature disclosed herein can be replaced with an alternative feature serving the same, equivalent, or similar purpose. I. Nanoparticles

[0072] A variety of different nanoparticles can be employed, including lipid nanoparticles (LNPs), polymeric nanoparticles, lipid polymer nanoparticles (LPNPs), protein and peptide-based nanoparticles, DNA dendrimers and DNA-based nanocarriers, carbon nanotubes, microparticles, microcapsules, inorganic nanoparticles, peptide caged nanoparticles, exosomes, etc. (e.g., Riley and Vermerris Nanomaterials 2017,7,94; Thomas et al.,Molecules 2019,24,3744; Bochicchio et al.,Pharmaceutics 2021,13,198; Munagala et al.,Cancer Letters 2021,505,58; Fu et al.,2020 NanoImpact 20,100261;and Neshat et al. 2020 Current Opin.Biotechnol.66:1-10).

[0073] If necessary, the nanoparticles can be targeted to cell types using targeting ligands that recognize, for example, target cell receptors. Examples of targeting ligands include carbohydrates (e.g., galactose, mannose, glucose, galactomannan), endogenous ligands (e.g., folic acid, transferrin), antibodies (e.g., anti-HER2 antibodies, hD1), proteins / peptides (e.g., RGD, epidermal growth factor, low density lipoprotein) and peptides. (For example, Teo et al., Advanced Drug Delivery Reviews 2016, 98, 41.)

[0074] A feature of the present application is the use of nanoparticles to deliver DNA. In different embodiments, the nanoparticles are used to deliver cytoplasmic DNA sensing inhibitors, immunosuppressants, phagocytic cellsAdditional compounds can be delivered, such as a reducing compound, an additional therapeutic compound, where one or more additional compounds are provided in a different nanoparticle; and where one or more additional compounds are provided in the same nanoparticle as the DNA vector, for example, a DNA vector and a cytoplasmic DNA sensing inhibitor, or a DNA vector, a cytoplasmic DNA sensing inhibitor and an immune cell modulating agent. "Compound" includes small molecules, macromolecules (e.g., therapeutic proteins and antibodies), and nucleic acids.

[0075] The fabrication of various nanoparticles and the incorporation of nucleic acids and other compounds are well known in the art and are exemplified in various publications throughout the discussion in Section I. In general, the exposure kinetics of nanoparticle cargo (e.g., DNA and / or inhibitors) can be influenced by exposing DNA to different compounds in different environments or by associating them with different structures.

[0076] Examples of publications illustrating the incorporation of nucleic acids in certain nanoparticles, such as LPNPs and LNPs, include Teo et al., Advanced Drug Delivery Reviews 2016, 98, 41; Bochicchio et al., Pharmaceutics 2021, 13, 198; Mahzabin and Das, IJPSR 2021, 12(1), 65; and Teixeira et al., Progress in Lipid Research 2017, 1 (each of which is incorporated herein by reference in its entirety). Such publications also point out the advantage of LPNPs in that they can provide a variety of structures that interact with nucleic acids and small molecules, thereby influencing the desired release kinetics. Factors that influence the incorporation of small molecules into nanoparticles include hydrophobicity and the presence of ionizable moieties. (See, e.g., Nii and Ishii, International Journal of Pharmaceutics 2005, 298, 198; and Chen et al, Journal of Controlled Release 2018, 286, 46).

[0077] In one embodiment, the compound (e.g., cytoplasmic DNA sensing inhibitor and / or immune cell modulator) is linked with fatty acid to increase hydrophobicity. Examples of fatty acids that can be linked with small molecules include those by Chen et al., Journal of Controlled Release 2018,286,46-54. IA lipid-based delivery system

[0078] Lipid-based delivery systems involve the use of lipids as components. Examples of lipid-based delivery systems include liposomes, LNPs, micelles, extracellular vesicles, etc.

[0079] "Lipid nanoparticle" or "LNP" refers to lipid-based vesicles with nanoscale dimensions that are useful for delivery of nucleic acid molecules. In different embodiments, the nanoparticles are about 10 nm to about 1000 nm, about 50 nm to about 500 nm, or about 50 nm to about 200 nm.

[0080] DNA is negatively charged.Therefore, it is beneficial for LNP to include cationic lipid, such as amino lipid.Exemplary amino lipids are described in U.S. Patent Nos. 9,352,042, 9,220,683, 9,186,325, 9,139,554, 9,126,966, 9,018,187, 8,999,351, 8,722,082, 8,642,076, 8,569,256, 8,466,122 and 7,745,651 and U.S. Patent Publication No. 2003 / 0133636. Nos. 2016 / 0213785, 2016 / 0199485, 2015 / 0265708, 2014 / 0288146, 2013 / 0123338, 2013 / 0116307, 2013 / 0064894, 2012 / 0172411, and 2010 / 0117125, all of which are incorporated herein in their entirety. In certain embodiments, the LNP comprises an amino lipid as described in U.S. Patent No. 9,512,073, which is incorporated herein in its entirety.

[0081] The terms "cationic lipid" and "amino lipid" are used interchangeably herein and include lipids and their salts that have one, two, three or more fatty acid or fatty alkyl chains and pH-adjustable amino groups (e.g., alkylamino or dialkylamino groups). Cationic lipids are usually protonated (i.e., positively charged) at pH levels below the pKa of the cationic lipid, and are substantially neutral at pH levels above the pKa. Cationic lipids can also be titratable cationic lipids. In certain embodiments, cationic lipids include a protonatable tertiary amine (e.g., pH-titrateable) group; a C18 alkyl chain (wherein each alkyl chain can independently have one or more double bonds, one or more triple bonds); and an ether, ester, or ketal bond between the head group and the alkyl chain.

[0082] The cationic lipids were 1,2-dilinoleyloxy-N,N-dimethylaminopropane (DLinDMA), 1,2-dilinolenyloxy-N,N-dimethylaminopropane (DLenDMA), 1,2-di-γ-linolenyloxy-N,N-dimethylaminopropane (γ-DLenDMA), 2,2-dilinoleyl-4-(2-dimethylaminoethyl)-[1,3]-dioxolane (DLin-K-C), and 1,2-dilinoleyl-4-(2-dimethylaminoethyl)-[1,3]-dioxolane (DLin-K-C). 2-DMA, DLin-C2K-DMA, XTC2, C2K), 2,2-Dilinoleyl-4-dimethylaminomethyl-[1,3]-dioxolane (DLin-K-DMA), Dilinoleylmethyl-3-dimethylaminopropionate (DLin-M-C2-DMA, also known as MC2), (6Z,9Z,28Z,31Z)-Heptatriaconta-6,9,28,31-tetraen-19-yl 4-(dimethylamino)butanoate (DLin-M-C3-DMA, also known as MC3), salts thereof, and mixtures thereof. Other cationic lipids include 1,2-distearyloxy-N,N-dimethyl-3-aminopropane (DSDMA), 1,2-dioleyloxy-N,N-dimethyl-3-aminopropane (DODMA), 2,2-dilinoleyl-4-(3-dimethylaminopropyl)-[1,3]-dioxolane (DLin-K-C3-DMA), 2,2-dilinoleyl-4-(3-dimethylaminobutyl)-[1,3]-dioxolane (DLin-K-C4-DMA), DLen-C2K-DMA, γ-DLen-C2K-DMA, and (DLin-MP-DMA) (also known as 1-B11).

[0083] Further cationic lipids include 2,2-dilinoleyl-5-dimethylaminomethyl-[1,3]-dioxane (DLin-K6-DMA), 2,2-dilinoleyl-4-N-methylpepiazino-[1,3]-dioxolane (DLin-K-MPZ), 1,2-dilinoleylcarbamoyloxy-3-dimethylaminopropane (DLin-C-DAP), 1,2-dilinoleyloxy-3-(dimethylamino)acetoxypropane (DLin-DAC), and 1,2-dilinoleyloxy-3-morpholinopropane (DLin-M-DAC). Pan (DLin-MA), 1,2-dilinoleoyl-3-dimethylaminopropane (DLinDAP), 1,2-dilinoleylthio-3-dimethylaminopropane (DLin-S-DMA), 1-linoleoyl-2-linoleyloxy-3-dimethylaminopropane (DLin-2-DMAP), 1,2-dilinoleyloxy-3-trimethylaminopropane chloride salt (DLin-TMA.Cl), 1,2-dilinoleoyl-3-trimethylaminopropane chloride salt (DLin-TAP.Cl), 1,2-dilinoleyloxy-3-(N-methylpiperazino)propane (DLin-MPZ), 3-(N,N-dilinoleylamino)-1,2-propanediol (DLinAP), 3-(N,N-dioleylamino)-1,2-propanediol (DOAP), 1,2-dilinoleyloxo-3-(2-N,N-dimethylamino)ethoxypropane (DLin-EG-DMA), N,N-dioleyl-N,N-dimethylammonium chloride (DODAC), N-(1-(2,3-dioleyloxy) )propyl)-N,N,N-trimethylammonium chloride (DOTMA), N,N-distearyl-N,N-dimethylammonium bromide (DDAB), N-(1-(2,3-dioleoyloxy)propyl)-N,N,N-trimethylammonium chloride (DOTAP), 3-(N-(N′,N′-dimethylaminoethane)-carbamoyl)cholesterol (DC-Chol), N-(1,2-dimyristyloxyprop-3-yl)-N,N-dimethyl-N-hydroxyethylammonium bromide amide (DMRIE), 2,3-dioleyloxy-N-[2(sperminecarboxamido)ethyl]-N,N-dimethyl-1-propanaminium trifluoroacetate (DOSPA), dioctadecylamidoglycylspermine (DOGS), 3-dimethylamino-2-(cholest-5-ene-3-β-oxybutane-4-oxy)-1-(cis,cis-9,12-octadecadienoxy)propane (CLinDMA), 2-[5′-(cholest-5-ene-3-β-oxy)-3′-oxapentoxy] -3-Dimethyl-1-(cis,cis-9',1-2'-octadecadienoxy)propane (CpLinDMA), N,N-Dimethyl-3,4-dioleyloxybenzylamine (DMOBA), 1,2-N,N'-Dioleylcarbamyl-3-dimethylaminopropane (DOcarbDAP), 1,2-N,N'-Dilinoleylcarbamyl-3-dimethylaminopropane (DLincarbDAP), dexamethasone-spermine (DS) and disubstituted spermine (D2S), or mixtures thereof.

[0084] Many commercially available formulations of cationic lipids can be used, such as LIPOFECTIN® (containing DOTMA and DOPE, available from GIBCO / BRL) and LIPOFECTAMINE® (containing DOSPA and DOPE, available from GIBCO / BRL).

[0085] Additional ionizable lipids that can be used include C12-200, 306Oi10, MC3, cKK-E12, bCKK-E12, Lipid 5, Lipid 9, ATX-002, ATX-003, and Merck-32. Merck-32 is described in U.S. Patent Application Publication No. 2017 / 0367988.

[0086] In further embodiments, the cationic lipid can be present in an amount from about 10% by molar ratio of the LNP to about 85% by molar ratio of the LNP, or from about 50% by molar ratio of the LNP to about 75% by molar ratio of the LNP.

[0087] LNPs can include neutral lipids. Neutral lipids include lipid species that exist in uncharged or neutral zwitterionic form at physiological pH. Such lipids include diacylphosphatidylcholine, diacylphosphatidylethanolamine, ceramide, sphingomyelin, dihydrosphingomyelin, cephalin, and cerebroside. The selection of neutral lipids is generally based on considerations such as particle size and stability. In certain embodiments, the neutral lipid component can be a lipid having two acyl groups (e.g., diacylphosphatidylcholine and diacylphosphatidylethanolamine).

[0088] Lipids with a variety of acyl chain groups of different chain lengths and degrees of saturation are available, or can be isolated or synthesized. In certain embodiments, lipids containing saturated fatty acids with carbon chain lengths ranging from C14 to C22 can be used. In certain embodiments, lipids with mono- or di-unsaturated fatty acids with carbon chain lengths ranging from C14 to C22 are used. Additionally, lipids with a mixture of saturated and unsaturated fatty acid chains can be used. Exemplary neutral lipids include 1,2-dioleoyl-sn-glycero-3-phosphatidyl-ethanolamine (DOPE), 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC), 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC), or phosphatidylcholine. Additionally, neutral lipids can be composed of sphingomyelin, dihydrosphingomyelin, or phospholipids with other head groups such as serine or inositol.

[0089] In further embodiments providing a neutral lipid, the neutral lipid can be present in an amount from about 0.1% by weight of the LNP to about 99% by weight of the LNP, or from about 5% by weight of the LNP to about 15% by weight of the LNP, e.g., about 1%, about 2%, about 3%, about 4%, about 5%, about 6%, about 7%, about 8%, about 9%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95%, or about 99%.

[0090] LNPs can include additional components such as sterols and polyethylene glycol. Sterols can provide fluidity to the LNPs. As used herein, "sterol" refers to naturally occurring sterols from plants (phytosterols) or animals (zoosterols) and non-naturally occurring synthetic sterols, all of which are characterized by the presence of a hydroxyl group at the 3-position of the steroid A ring. Suitable sterols include those traditionally used in the field of liposome, lipid vesicle or lipid particle preparation, most commonly cholesterol. Phytosterols include campesterol, sitosterol, stigmasterol, and the like. Sterols also include sterol-modified lipids, such as those described in U.S. Patent Application Publication No. 2011 / 0177156. In different embodiments providing a sterol, the sterol is present in an amount between about 1% by weight of the LNP and about 80% by weight of the LNP, or between about 10% by weight of the LNP and about 25% by weight of the LNP.

[0091] Polyethylene glycol (PEG) is a linear water-soluble polymer of repeating ethylene PEG units with two terminal hydroxyl groups. PEGs are classified by molecular weight, e.g., PEG 2000 has an average molecular weight of about 2000 daltons, and PEG 5000 has an average molecular weight of about 5000 daltons. Commercially available PEGs, such as those from Sigma Chemical Co., include monomethoxypolyethyleneglycol (MePEG-OH), monomethoxypolyethyleneglycol-succinate (MePEG-S), monomethoxypolyethyleneglycol-succinimidyl succinate (MePEG-S-NHS), monomethoxypolyethyleneglycol-amine (MePEG-NH2), monomethoxypolyethyleneglycol-tresylate (MePEG-TRES), and monomethoxypolyethyleneglycol-imidazolyl-carbonyl (MePEG-IM).

[0092] In certain embodiments of the PEG, the PEG has an average molecular weight of about 550 to about 10,000 daltons and is optionally substituted with alkyl, alkoxy, acyl, or aryl. In further embodiments, the PEG is substituted with methyl at the terminal hydroxyl position. In further embodiments, the PEG has an average molecular weight of about 750 to about 5,000 daltons, or about 1,000 to about 5,000 daltons, or about 1,500 to about 3,000 daltons, or about 2,000 daltons, or about 750 daltons.

[0093] PEG-modified lipids include PEG-dialkyloxypropyl conjugates (PEG-DAAs) as described in U.S. Patent Nos. 8,936,942 and 7,803,397. PEG-modified lipids (or lipid-polyoxyethylene conjugates) can have a variety of "anchor" lipid moieties to anchor the PEG moiety to the surface of the lipid vesicle. Examples of suitable PEG-modified lipids include PEG-modified phosphatidylethanolamines and phosphatidic acids, PEG-ceramide conjugates (e.g., PEG-CerC14 or PEG-CerC20) as described in U.S. Patent No. 5,820,873, PEG-modified dialkylamines, and PEG-modified 1,2-diacyloxypropan-3-amines. In certain embodiments, the PEG-modified lipids can be PEG-modified diacylglycerols and dialkylglycerols. In certain embodiments, the PEG can be in an amount of about 0.1% by weight of the LNP to about 50% by weight of the LNP, or about 5% by weight of the LNP to about 15% by weight of the LNP.

[0094] In further embodiments regarding LNP size, the LNPs prior to encapsulating nucleic acid have a size ranging from about 10 nm to about 500 nm, or from about 50 nm to about 200 nm, or from 75 nm to about 125 nm.

[0095] In certain embodiments of LNPs, the LNPs are described in Billingsley et al., Nano Lett. 2020,20,1578 or Billingsley et al., International Patent Publication No. WO 2021 / 077066, both of which are incorporated herein by reference in their entirety. Billingsley et al. and WO2021 / 077066 describe LNPs comprising lipid-immobilized PEG, cholesterol, phospholipids, and ionizable lipids. In certain embodiments, the LNPs comprise a C14-4 polyamine core and / or have a particle size of about 70 nm. C14-4 has the following structure: [ka]

[0096] In certain embodiments, the LNPs are composed of cationic lipids or lipopeptides as described by U.S. Pat. No. 10,493,031, U.S. Pat. No. 10,682,374, or WO2021 / 077066, each of which is incorporated herein by reference in its entirety. In certain embodiments, the LNPs comprise cationic lipids, cholesterol-based lipids, and / or one or more PEG-modified lipids. In certain embodiments, the LNPs comprise cKK-E12 (Dong et al., PNAS (2014) 111(11), 3955): [ka]

[0097] In certain embodiments, the LNP comprises a modified form of cKK-E12, referred to herein as "bCKK-E12," having the following structure: [ka]

[0098] In certain embodiments, the LNPs comprise lipids 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 described by Sabnis et al., Molecular Therapy 2018, 26:6, 1509-1519, which is incorporated herein by reference in its entirety. In certain embodiments, the LNPs comprise lipids 5, 8, 9, 10, or 11 described by Sabnis et al.

[0099] The structure of Lipid5 from Sabnis et al. is as follows: [ka]

[0100] The structure of Lipid9 by Sabnis et al. is as follows: [ka]

[0101] Additional lipids that may be utilized include Roces et al., Pharmaceutics, 2020, 12, 1095; Jayaraman et al., Angew. Chem. Int. Ed., 2012, 51, 8529-8533; Maier et al., www.moleculartherapy.org, 2013, Vol. 21, No. 8, 1570-1578; Liu et al., Adv. Mater. 2019, 31, 1902575, e.g., BAMEA-O16B; Cheng et al., Adv. Mater., 2018, 30, 1805308, e.g., 5A2-SC8; Hajj and Ball, Small, 2019 15, 1805097, e.g., 306Oi10; Du et al., U.S. Patent Application Publication No. 20160376224; and Tanaka et al., Adv. Funct. Mater., 2020, 30, 1910575; each of which is incorporated by reference in its entirety.

[0102] In a further embodiment, the nanoparticle is a LNP. In a further embodiment, the LPN (mol%) comprises, consists essentially of, or consists of the following components: (1) about 20% to about 65% of one or more cationic lipids, about 1% to about 50% of one or more phospholipids, about 0.1% to 10% of one or more PEGylated lipids, and about 0% to about 70% of cholesterol; and (2) about 20% to about 50% of one or more cationic lipids, about 5% to about 20% of one or more phospholipids, about 0.1% to about 5% of one or more PEGylated lipids, and about 20% to about 60% of cholesterol. In a further embodiment, the lipid of the phospholipid is a neutral lipid; and the lipid of the phospholipid is DOPE or DSPC.

[0103] In further embodiments, the LPN (mol %) comprises, consists essentially of, or consists of the following components: (1) cKK-E12 (further described in IA below), about 35%; C14-PEG2000, about 2.5%; cholesterol, about 46.5%; and DOPE, about 16%; (2) bCKK-E12 (further described in IA below), about 35%; C14-PEG2000, about 2.5%; cholesterol, about 46.5%; and DOPE, about 16%; (3) Lipid9 (described further in Sabnis et al., and in the IA, infra), about 50%; C14-PEG2000, about 1.5%; cholesterol, about 38.5%; and DSPC, about 10%; or (4) Lipid5 (described further in Sabnis et al., and in the IA, infra), about 50%; C14-PEG2000, about 1.5%; cholesterol, about 38.5%; and DSPC, about 10%; and (5) ionizable lipid, about 50%; DSPC, about 10%; cholesterol, about 37.5%; and stabilizer (PEG-lipid), about 2.5%; or (6) GenVoy-ILM TM LNP (Precision NanoSystems). IB Polymer-Based Nanoparticles

[0104] Polymer-based delivery systems can be made from a variety of natural and synthetic materials. DNA and other compounds can be encapsulated in the polymer matrix of polymer nanoparticles or adsorbed or bound to the surface of the nanoparticles. Examples of polymers commonly used for nucleic acid delivery include poly(lactic-co-glycolic acid) (PLGA), polylactic acid (PLA), poly(ethylenimine) (PEI) and PEI derivatives, chitosan, dendrimers, polyanhydrides, polycaprolactone polymethacrylates, poly-L-lysine, pullulan, dextran, and hyaluronic acid, poly-β-aminoesters. (Thomas et al.,Molecules 2019,24,3744.)

[0105] In certain embodiments, the polymeric nanoparticles have different sizes ranging from about 1 nm to about 1000 nm, from about 10 nm to about 500 nm, from about 50 nm to about 200 nm, from about 100 nm to about 150 nm, and less than about 150 nm. IC - lipid polymer nanoparticles

[0106] Lipid-polymer nanoparticles are hybrid nanoparticles that provide both lipid and polymer components, and as such can be considered LNPs or LPNPs. LPNP configurations can provide an outer polymer and an inner lipid, or an outer lipid and an inner polymer. The presence of two different types of materials facilitates the design of nanoparticles that provide delayed release of components. Different lipid and polymer components can be selected taking into account the substance to be delivered (e.g., cytoplasmic DNA-sensing inhibitors and DNA vectors) with guidance provided in IA supra and IB supra and in the art. (e.g., Teo et al., Advanced Drug Delivery Reviews 2016, 98, 41; Bochicchio et al., Pharmaceutics, 2021 13, 198; Mahzabin and Das, IJPSR 2021, 12(1), 65; Teixeira et al., Progress in Lipid Research, 2018, 1.) ID Protein and Peptide-Based Nanoparticles

[0107] Protein and peptide-based systems can use a wide variety of proteins and peptides. Examples of proteins include gelatin and elastin. Peptide-based systems can use CPPs, for example.

[0108] CPPs are short peptides (6-30 amino acid residues) that may allow therapeutic molecules to penetrate into cells. Most CPPs consist mainly of arginine and lysine residues and are cationic and hydrophilic, but CPPs can also be amphipathic, anionic, and hydrophobic. CPPs can be derived from natural biomolecules (e.g., the HIV-1 protein Tat) or obtained by synthetic methods (e.g., poly-L-lysine, polyarginine) (Singh et al., Drug Deliv. 2018;25(1):1996-2006). Examples of CPPs include cationic CPPs (highly positively charged) such as Tat peptide, penetratin, protamine, poly-L-lysine, and polyarginine; amphipathic CPPs (chimeric or fusion peptides constructed from different sources and containing both positively and negatively charged amino acid sequences) such as transportan, VT5, bactenecin-7 (Bac7), proline-rich peptides (PPRs), SAP (VRLPPP)3, TP10, pep-1, and MPG; membrane-tropic CPPs (which simultaneously exhibit hydrophobic and amphipathic properties and contain both large aromatic and small residues) such as H625, SPIONs-PEG-CPP, and NP; and hydrophobic CPPs (containing only non-polar motifs or residues) such as SG3, PFVYLI, pep-7, and fibroblast growth factor.

[0109] Protein and peptide nanoparticles can be provided in different sizes ranging, for example, from about 1 nm to about 1000 nm, from about 10 nm to about 500 nm, from about 50 nm to about 200 nm, from about 100 nm to about 150 nm, or less than about 150 nm. IE Peptide Cage Nanoparticles

[0110] Peptide cage-based delivery systems can be fabricated from proteinaceous materials that can be assembled into cage-like structures that form a constrained internal environment. Peptide cages can include proteinaceous shells (e.g., structures with internal cavities that have natural access to solvent or can do so by altering solvent concentration, pH, equilibrium ratios) that self-assemble to form protein cages. Monomers of protein cages can be naturally occurring or mutants that contain amino acid substitutions, insertions, deletions (fragments, etc.).

[0111] Various types of protein "shells" can be assembled and loaded with various types of materials. Protein cages can be made using viral coat proteins (e.g., from the cowpea chlorophyll spot virus protein coat), as well as non-viral proteins (e.g., U.S. Pat. Nos. 6,180,389 and 6,984,386, U.S. Patent Application Publication No. 20040028694, and U.S. Patent Application Publication No. 20090035389, the disclosures of each of which are incorporated herein by reference).

[0112] Examples of protein cages derived from non-viral proteins include ferritins and apoferritins from eukaryotes or prokaryotes, such as the 12 and 24 subunit ferritins; and heat shock proteins (HSPs), such as the class of 24 subunit heat shock proteins that form the inner core space, the small HSP of Methanococcus jannaschii, the 12-mer Dsp HSP of Escherichia coli, and the MrgA proteins.

[0113] In certain embodiments, the protein cages have different core sizes, such as ranging from about 1 nm to about 1000 nm, from about 10 nm to about 500 nm, from about 50 nm to about 200 nm, from about 100 nm to about 150 nm, or less than about 150 nm. IF Exosomes

[0114] Exosomes are small biological membrane vesicles that can be used to deliver a variety of cargoes, including small molecules, peptides, proteins, and nucleic acids. Exosomes generally range in size from about 30 nm to 100 nm and can be internalized by cells to deliver their cargo. The cargo can be associated with exosome surface structures or encapsulated within the exosome bilayer.

[0115] Exosomes can be modified in a variety of ways to facilitate cargo delivery and cellular targeting. Modifications to facilitate cargo transport include structures for associating with the cargo, such as protein scaffolds and polymers. Modifications for cellular targeting include targeting ligands and surface charge modifications. Publications describing the production, modification, and use of exosomes for delivery of different cargoes include Munagala et al., Cancer Letters 2021, 505, 58; Fu et al., 2020 NanoImpact 20, 100261; and Dooley et al., 2021 Molecular Therapy 29(5), 1729 (each of which is incorporated herein by reference). II. Cytoplasmic DNA sensing pathway inhibitors

[0116] The cytoplasmic DNA sensing pathway senses foreign DNA and triggers an immune response that leads to the production of inflammatory cytokines, inflammatory chemokines, and type I interferons. (For example, hypertext transfer protocol: / / www.genome.jp / dbget-bin / www_bget?pathway+hsa04623, the entirety of which is incorporated herein by reference). In order to reduce the immune response caused by DNA, a cytoplasmic DNA sensing pathway inhibitor can be provided. In different embodiments, a cGAS-STING and / or inflammasome pathway inhibitor is employed. A specific inhibitor that inhibits one or more targets can be provided as an inhibitor of each target or any target.

[0117] Various types of compounds can inhibit the production or activity of proteins involved in the cytoplasmic DNA sensing pathway and can be used as inhibitors. In certain embodiments, the cytoplasmic DNA sensing pathway inhibitor is a small molecule, an antibody, a peptide, a nucleic acid, or a target protein of a degrading agent (such as a protac or degrading agent). II.A. cGAS-STING Pathway Inhibitors

[0118] cGAS-STING pathway inhibitors may act directly on cGAS-STING pathway proteins such as cGAS, STING, TBK1, or on drugs that affect the cGAS-STING pathway. References describing cGAS-STING pathway inhibitor design and examples of inhibitors include Ding et al., Acta Pharmaceutica Sinica B 2020,10(12),2272 ("Ding"), Fu et al., iScience 2020,23,101026, Konno et al., Cell Rep. 2018,23(24),1112, US Patent Application Publication No. 20200291001, and Haag et al., Nature,2018,559,269-273, each of which is incorporated herein by reference.

[0119] Various compounds described herein, including cGAS-STING pathway inhibitors, can be provided as pharmaceutically acceptable salts. "Pharmaceutically acceptable salts" refers to salts suitable for administration. Depending on the compound, pharmaceutically acceptable salts include acid addition salts and base salts. Pharmaceutically acceptable acid addition salts include the following: hydrochloride, hydrobromide, hydroiodide, nitrate, sulfate, bisulfate, phosphate, acid phosphate, isonicotinate, carbonate, bicarbonate, acetate, lactate, salicylate, citrate, tartrate, propionate, butyrate, pyruvate, oxalate, malonate, pantothenate, bitartrate, ascorbate, succinate, maleate, gentisinate, fumarate, gluconate, glucaronate, saccharate, formate, benzoate, glutamate, methanesulfonate, ethanesulfonate, benzenesulfonate, p-toluenesulfonate, and pamoate (i.e., 1,1′-methylene-bis-(2-hydroxy-3-naphthoate)). Suitable base salts include aluminum, calcium, lithium, magnesium, potassium, sodium, zinc, bismuth, diethanolamine salts, etc. Additionally, various amino acids can be employed as pharma- ceutically acceptable salts.

[0120] In certain embodiments, the STING inhibitor is selected from 1-oxo-1,2,3,4-tetrahydroisoquinolin-4-yl carboxylic acid (44), 9-amino-6-chloro-2-methoxyacridine (59), hydrochloroquine (60): [ka] [ka] [ka]

[0121] GSK690693 is an AMP-activated protein kinase (AMPK) / AKT inhibitor and is an example of an inhibitor that affects the cGAS-STING pathway. AMPK / AKT activity affects the cyclic cGAS-STING pathway by decreasing phosphorylation of ULK1, which allows ULK1 to phosphorylate STING and inhibit STING activity. Examples of AMPK inhibitors, including GSK690693, are provided in Konno et al., Cell Rep. 2018,23(4),1112.

[0122] Additional references providing additional STING inhibitors, STING inhibitor scaffolds and motifs, and design considerations include: Decout et al., Nat. Rev. Immunol., 2021, Sep;21(9):548-569; Dubensky et al., U.S. Pat. No. 10,189,873; Katibah et al., U.S. Pat. Appl. Pub. No. 20180369268; Seidel et al., International Pat. Appl. Pub. No. WO2020 / 150439; Roush et al., U.S. Pat. Appl. Pub. No. 20200172534; Roush et al., U.S. Pat. Appl. Pub. No. 2021236466; Glick et al., International Pat. Appl. Pub. No. WO2022 / 140410; Hong et al., Proc Natl Acad. Sci US A., 2021, Jun 15;118(24); and Hong et al., Journal of Molecular Cell Biology, 2022, 14(2), njac005; each of these publications is incorporated by reference in its entirety.

[0123] In different embodiments, the inhibitor is as provided in Table 1, or a pharma- ceutically acceptable salt thereof.

[0124] [Table 1] JPEG2024540994000011.jpg143170

[0125] In different embodiments, the cGAS inhibitor is any of the following: quinacrine hydrochloride (55), ethidium bromide (56), actinomycin (57), quinacrine (58), 9-amino-6-chloro-2-methoxyacridine (59), hydroxychloroquine (60), [ka] [ka]

[0126] Ding describes compounds 55, 56, and 57 as indirect cGAS inhibitors that intercalate DNA, and compounds 58 to 64 as indirect cGAS inhibitors that inhibit 2´,3´-cGAMP synthesis.

[0127] Other publications providing cGAS inhibitors, cGAS inhibitor scaffolds and motifs, and design considerations include: Decout et al., Nat. Rev. Immunol., 2021 Sep;21(9):548-569; Vincent et al., Nat. Commun., 2017,8:750; Lama et al., Nat. Commun., 2019,May 21;10(1):2261; Obioma et al., US Patent No. 10,738,056; Hong et al., Journal of Molecular Cell Biology, 2022,14(2),njac005; Zhao et al., J. Chem. Inf.Model, 2020,60,3265-3276; and Padilla-Salinas et al., J. Org. Chem., 2020, 85, 1579-1600; each of these publications is incorporated by reference in its entirety.

[0128] In different embodiments, the inhibitor is as provided in Table 2, or a pharmaceutical salt thereof.

[0129] [Table 2] JPEG2024540994000015.jpg131170

[0130] In a different embodiment, the TBK1 inhibitor is dovitinib. [ka] JPEG2024540994000017.jpg162170

[0131] References providing additional TBK1 inhibitors, TBK1 inhibitor scaffolds and motifs, and design considerations include: Thomson et al., Expert Opinion on Therapeutic Patents, 2021, 31:9 785-794; Chekler et al., U.S. Patent Application Publication No. 20210214339; Newton and Stewart, U.S. Patent No. 11,058,686; Karra et al., International Patent Publication No. WO2019 / 079373A1; Bigi et al., U.S. Patent No. 9,994,547; Schulze et al., U.S. Patent No. 10,894,784; Hassan and Yan, Parmacol. Res., 2016, 111:336-342; Li et al., Int. J. Cancer 2014, 134:1972-1980; Alam et al., International Journal of Biological Macromolecules, 2022, 2027:1022-1037; Perrior et al., U.S. Patent No. 8,962,609; and Du et al., U.S. Patent No. 10,316,049; all of which are incorporated by reference herein.

[0132] In certain embodiments, the inhibitor is as provided in Table 3, or a pharmaceutical salt thereof.

[0133] [Table 3] JPEG2024540994000019.jpg193170

[0134] II.B. Inflammasome Pathway Inhibitors

[0135] Inflammasome pathway inhibitors can act directly on inflammasome pathway proteins, such as the Absent in Melanoma-2 (AIM2) protein, or on drugs that affect the inflammasome pathway. Certain DNA sequences, such as TTAGGG repeats commonly found in mammalian telomeric DNA, bind with AIM2 to suppress innate immune activation. (Kaminski et al, The Journal of Immunology, 2013, 191, 3876). Such sequences can also inhibit other innate responses, such as cGAS and STING. An example of an AIM2 inhibitor is A151, a synthetic oligonucleotide containing four repeats of the TTAGGG motif, with the following nucleotide sequence, where the bases are linked by phosphorothioate bonds: 5′-TTAGGGTTAGGGTTAGGGTTAGGG-3′ (SEQ ID NO:1); and 5′-TTAGGGTTAGGGTTAGGGTTAGGG-3′ (SEQ ID NO:2), containing phosphodiester bonds. Additional oligonucleotide sequences include other types of modified SEQ ID NO:2, such as those with the same nucleotide sequence but with different modified backbones. Such nucleotide sequences can also be used as cGAS and STING inhibitors. As cGAS and STING inhibitors, they can be incorporated into DNA or DNA vectors. III. DNA Vectors

[0136] A DNA vector contains a transgene and one or more regulatory elements that affect RNA expression or processing from the transgene. The RNA produced can be, for example, functional or can code for a specific protein. Regulatory elements include, for example, various elements that regulate the transcription of functional RNA, the production of the protein encoded by the transgene, and the processing of the protein. Regulatory elements that can be present include enhancer sequences, introns, post-transcriptional regulatory elements, polyadenylation and termination signal sequences, on-off switches, cell-specific regulators, and internal ribosome entry sites. In addition to regulatory elements, some DNA vectors can contain elements such as terminal inverted repeats, elements that facilitate plasmid replication or selection, sequences that facilitate protein secretion, and the like. There can be multiple transgenes, which can be of the same type or different; and / or multiple elements, which can be of the same type or different.

[0137] The DNA vector may further comprise one or more regulatable elements. Such elements provide an on / off switch for gene expression. Regulatable elements include tissue-specific elements and drug-responsive transcription (promoter / enhancer) elements. Examples of regulatable elements include tetracycline-inducible elements, druggable ribozymes, druggable toe-hold switches, microRNA-responsive genes (e.g., mRNA stability or protein translation), morpholino-responsive mRNAs (e.g., splicing or mRNA stability), suppressor tRNA-regulated genes, genes controlled by alternative splicing, and druggable degrons.

[0138] In one embodiment, the DNA vector is used in gene therapy. Gene therapy includes both loss-of-function and gain-of-function gene defects. The term "loss-of-function" in reference to a genetic abnormality refers to a genetic mutation in which the protein encoded by the gene loses some or all of the functions normally associated with the wild-type protein. The term "gain-of-function" in reference to a genetic defect refers to a mutation in a gene that causes the protein encoded by the gene to gain a function not normally associated with the wild-type protein, causing or contributing to a disease or disorder. A gain-of-function mutation is a deletion, addition, or substitution of nucleotides or nucleotides in a gene that results in a change in the function of the encoded protein. In certain embodiments, a gain-of-function mutation changes the function of the mutant protein or causes it to interact with other proteins. In certain embodiments, a gain-of-function mutation causes a reduction or elimination of the normal wild-type protein, for example, by interaction of the altered mutant protein with the normal wild-type protein.

[0139] Various types of DNA vectors can be employed, including minicircles, nanoplasmids, open linear double-stranded DNA, closed linear double-stranded DNA (CELiD / ceDNA / Doggybone DNA), single-stranded circular DNA, and single-stranded linear DNA.

[0140] In one embodiment, the DNA vector contains a balance of motifs that enhance gene expression and sequences and motifs that induce immune stimulation in a mammal, for a particular mammal selected as a target. Gene expression in a particular mammal can be enhanced, for example, by optimizing codons, reducing CpGs, and reducing RNA secondary structures and unstable motifs. Examples of immune stimulatory motifs that can be reduced include CpGs, pyrimidine-rich sequences, palindromic sequences, etc.

[0141] In different embodiments, the transgene is a viral antigen, a bacterial antigen, a therapeutic protein, a short hairpin RNA (shRNA), a small interfering RNA (siRNA), a microRNA (miRNA), an RNA i、Encode ribozymes, antisense RNA, CRISPR / Cas9 constructs, zinc finger nucleases (ZFNs), or transcription activator-like effector nucleases (TALENs). III.A. Promoters

[0142] A promoter is generally located 5' to the polynucleotide sequence to be expressed and is operably linked to the polynucleotide sequence. For example, a promoter is operably linked to a polynucleotide sequence if it is capable of affecting the expression of the sequence (e.g., the sequence is under the transcriptional control of the promoter). A promoter binds RNA polymerase and necessary transcription factors to initiate transcription from the polynucleotide sequence. The promoter sequence determines the direction of transcription and which DNA strand is transcribed.

[0143] The coding sequence may be operably linked to the regulatory sequence in sense or antisense orientation. In certain embodiments, the promoter is a heterologous promoter. The term "heterologous promoter" refers to a promoter that is not found operably linked to a given coding sequence in nature.

[0144] The promoter sequence can provide proximal and more distal upstream elements. In one embodiment, the promoter comprises an enhancer element. An "enhancer" is a nucleotide sequence that can stimulate promoter activity and can be a native element of the promoter or a heterologous element that is inserted to increase the level or tissue specificity of the promoter.

[0145] Promoters can be derived from different sources or generated from different elements, for example, promoters can be derived from a native gene, can be composed of different elements derived from different naturally occurring promoters, or can be composed of synthetic nucleotide sequences.

[0146] Different promoters can be selected to direct expression of the nucleotide sequence in different tissues or cell types, or at different stages of development, or in response to different environmental conditions, or in response to the presence or absence of drugs or transcriptional cofactors. Ubiquitous, cell type-specific, tissue-specific, developmental stage-specific, and conditional promoters are well known in the art. Examples of promoters include the phosphoglycerate kinase (PKG) promoter, CAG (a complex of CMV enhancer, chicken beta actin promoter (CBA), and rabbit beta globin intron), NSE (neuron specific enolase), and NeuN promoters. SV40 early promoter, mouse mammary tumor virus LTR promoter, adenovirus major late promoter (Ad MLP), herpes simplex virus (HSV) promoter, cytomegalovirus (CMV) promoters such as the CMV immediate early promoter region (CMVIE), SFFV promoter, Rous sarcoma virus (RSV) promoter, synthetic promoters, and hybrid promoters. Other promoters may be of human or other species, including mouse. Common promoters include: human cytomegalovirus (CMV) immediate early gene promoter, Rous sarcoma virus long terminal repeat, [β]-actin, rat insulin promoter, human α1 antitrypsin (hAAT) promoter, transthyretin promoter, TBG promoter and other liver-specific promoters, muscle-specific promoters like the desmin promoter, EF1α promoter, CAG promoter and other constitutive promoters, hybrid promoters with multiple tissue specificity, neuron-specific promoters like synapsin, and glyceraldehyde-3-phosphate dehydrogenase promoter. In addition, sequences from non-viral genes such as the mouse metallothionein gene can also be employed. A variety of promoter sequences are commercially available, see, for example, Stratagene (San Diego, CA). III.B. Additional Features

[0147] Additional elements that may be present include introns, enhancers, polyadenylation and termination signals, post-translational regulatory elements, 5' and 3' inverted repeats (ITRs), on-off switches (e.g., rheostats), cell-specific regulators (e.g., micoRNA binding elements), internal ribosome entry sites, or other elements that affect expression or stability of the encoded sequence; or protein processing (e.g., secretion signal sequences). Examples of different element arrangements include 5' to 3' promoters / enhancers, transgenes, post-transcriptional regulatory elements, polyadenylation and termination signals.

[0148] Polyadenylation sequences are important for the nuclear transport, translation, and stability of mRNA. Examples of polyadenylation sequences include HGH, SV40 late, bGHpA, synthetic polyA (SPA), bGH, mutant BGH, and HSV TK. (Wang and Guo 2020,104,5673; and Powell et al.,Discovery Medicine 2015,19(102),49.).

[0149] Viral post-transcriptional regulatory elements are cis-acting elements involved in the nuclear export of intronless viral RNA, such as the Hepatitis B virus PRE and the Woodchuck Response Element (WRE) (Powell et al., Discovery Medicine 2015,19(102),49).

[0150] The presence of an intron between the promoter and the transgene enhances gene expression and RNA processing. (Powell et al., Discovery Medicine 2015,19(102),49) Examples of introns include MVM, hCMV intron, hEF1 promoter intron, chimeric intron, modified SV40 intron, and β-globin intron.

[0151] Optionally, the encoded polypeptide can be expressed with a secretory signal sequence that facilitates extracellular secretion of the polypeptide. The term "secretory signal sequence" refers to an amino acid sequence that functions to enhance secretion of an operably linked polypeptide from a cell compared to the level of secretion observed for a polypeptide lacking a secretory signal sequence. Essentially all, or even most, of the polypeptide need not be secreted, as long as the level of secretion is enhanced compared to the native polypeptide. In different embodiments, at least 95%, 97%, 98%, or 99% of the polypeptide is secreted. Generally, the secretory signal sequence is cleaved in the endoplasmic reticulum and may be cleaved prior to secretion. As long as secretion of the polypeptide from the cell is facilitated and the polypeptide is functional, the secretory signal sequence need not be cleaved.

[0152] The secretory signal sequence can be derived in whole or in part from a secretory signal of a secreted polypeptide (i.e., from a precursor) and / or can be synthetic in whole or in part. The length of the secretory signal sequence is not critical and can be, for example, from about 10-15 to 50-60 amino acids in length. Known secretory signals from secreted polypeptides can be altered or modified (e.g., by amino acid substitution, deletion, truncation, or insertion) so long as the resulting secretory signal sequence functions to enhance secretion of the operably linked polypeptide. The secretory signal sequence can comprise, consist essentially of, or consist of a naturally occurring secretory signal sequence or a variant thereof. Examples of synthetic or artificial secretory signal peptides are described in Barash et al., Biochem. Biophys. Res. Comm. 294, 835 (2002). III.D. Therapeutic Proteins

[0153] DNA vectors can deliver a variety of different transgenes that can be expressed to provide a protein with a desired activity. Examples of transgenes include those that provide a healthy copy of a gene to a genetically defective subject, or new genes that help treat a disease or disorder, or code for a protein that provides a beneficial effect.

[0154] In different embodiments, the transgene encodes: GAA (acid alpha-glucosidase) for the treatment of Pompe disease; TPP1 (tripeptidyl peptidase-1) for the treatment of late childhood neuronal ceroid lipofuscinosis type 2 (CLN2); ATP7B (copper-transporting ATPase2) for the treatment of Wilson's disease; alpha-galactosidase for the treatment of Fabry disease; ASS1 (argininosuccinate synthase) for the treatment of citrullinemia type 1; beta-glucocerebrosidase for the treatment of Gaucher disease type 1; beta-hexosaminidase A for the treatment of Tay-Sachs disease; SERPING1 (C1 protease inhibitor or C1 esterase inhibitor) for the treatment of hereditary angioedema (HAE) (also known as C1 inhibitor deficiency types I and II); or glucose-6-phosphatase for the treatment of glycogen storage disease type I (GSDI).

[0155] In different embodiments, the transgene encodes: insulin, glucagon, growth hormone (GH), parathyroid hormone (PTH), growth hormone releasing factor (GRF), follicle stimulating hormone (FSH), luteinizing hormone (LH), human chorionic gonadotropin (hCG), vascular endothelial growth factor (VEGF), angiopoietin, angiostatin, granulocyte colony stimulating factor (GCSF), erythropoietin (EPO), connective tissue growth factor (CTGF), basic fibroblast growth factor (bFGF), ), acidic fibroblast growth factor (aFGF), epidermal growth factor (EGF), transforming growth factor alpha (TGFα), platelet-derived growth factor (PDGF), insulin growth factor I or II (IGF-I or IGF-II), TGFβ, activin, bone morphogenetic proteins (BMPs), nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), neurotrophins NT-3 or NT4 / 5, ciliary neurotrophic factor (CNTF), glial cell line-derived neurotrophic factor (GDNF), neutrophin, agrin netrin-1 or netrin-2, hepatocyte growth factor (HGF), ephrin, noggin, sonic hedgehog, tyrosine hydroxylase, etc.

[0156] In different embodiments, the transgene encodes thrombopoietin (TPO), interleukins (IL-1 through IL-36), monocyte chemotactic proteins, leukemia inhibitory factor, granulocyte macrophage colony stimulating factor, Fas ligand, tumor necrosis factor alpha or beta, interferon alpha, beta, gamma, stem cell factor, flk-2 / flt3 ligand, IgG, IgM, IgA, IgD or IgE, chimeric immunoglobulins, antibodies, humanized antibodies, single chain antibodies, T cell receptors, chimeric T cell receptors, single chain T cell receptors, class I or class II MHC molecules. Antibodies and immunoglobulins can be provided, for example, to target cancer cells or other disease or disorder causing cells.

[0157] In different embodiments, the transgene encodes: CFTR (cystic fibrosis transmembrane conductance regulator protein), blood clotting (clotting) factors (Factor XIII, Factor IX (FIX), Factor VIII (FVIII), Factor X, Factor VII, Factor VIIa, or Protein C), gain of function blood clotting factors, erythropoietin, LDL receptor, lipoprotein lipase, ornithine transcarbamylase, β-globin, α-globin, spectrin, α-antitrypsin, adenosine deaminase (ADA), metal transporters (ATP7A or ATP7), sulfamidase, enzymes involved in lysosomal storage diseases (ARSA), hypoxanthine guanine phosphoribosyltransferase, β-25 glucocerebrosidase, sphingomyelinase, lysosomal storage diseases (ALS), ... Sosomal hexosaminidase, branched-chain ketoacid dehydrogenase, hormones, growth factors, insulin-like growth factor 1 or 2, platelet-derived growth factor, epidermal growth factor, nerve growth factor, neurotrophic factor-3 and -4, brain-derived neurotrophic factor, glial-derived growth factor, transforming growth factor α and β, cytokines, α-interferon, β-interferon, interferon-γ, interleukin-2, interleukin-4, interleukin-12, granulocyte-macrophage colony-stimulating factor, lymphotoxins, suicide gene products, herpes simplex virus thymidine kinase, cytosine deaminase, diphtheria toxin, cytochrome P450, deoxycytidine kinase, tumor necrosis factor, drug resistance proteins, tumor suppressor proteins (e.g., p53, Rb, Wt-1, NF1, VonVon Hippel-Lindau (VHL), Adenomatous Polyposis Coli (APC), Immunomodulatory Peptides, Tolerogenic or Immunogenic Peptides or Proteins Tregitope or hCDR1, Insulin, Glucokinase, Guanylate Cyclase 2D (LCA-GUCY2D), Retinal Pigment Epithelium-Specific 65kDa Protein (RPE65), Rab Escort Protein 1 (Chroideremia), LCA5 (LCA-Revasillin), Ornithine Ketoacid Aminotransferase (Rotor Atrophy), Retinoschisin 1 (X-linked Retinochalasis), X-linked Retinitis Pigmentosa GTPase (XLRP), MER Proto-Oncogene Tyrosine Kinase (MERTK) (Autosomal Recessive (AR) Retinitis Pigmentosa (RP)), ABCA4 (Stargardt), ACHM 2, 3, 4 (color blindness), anti-vascular endothelial growth factor (VEGF) agent polypeptides (such as bevacizumab, brolucizumab, ranibizumab, aflibercept), DFNB1 (connexin 26 deafness), USH1C (Usher syndrome 1C), PKD-1 or PKD-2 (polycystic kidney disease), TPP1 (tripeptidyl peptidase-1), sulfatase, N-acetylglucosamine-1-phosphate transferase, cathepsin A, GM2-AP, NPC1, VPC2, sphingolipid activating protein, or one or more donor sequences used as a repair template for genome editing.

[0158] In different embodiments, the transgene encodes: erythropoietin (EPO) for the treatment of anemia; interferon-α, interferon-β, interferon-γ for the treatment of various immune disorders, viral infections, and cancers; interleukins (ILs), including any one of IL-1 through IL-36, and corresponding receptors, for the treatment of various inflammatory disorders or immune deficiencies; chemokines, including chemokine (C-X-C motif) ligand 5 (CXCL5), for the treatment of immune disorders; and granulocyte colony-stimulating factor for the treatment of immune disorders such as Crohn's disease. (G-CSF); granulocyte-macrophage colony-stimulating factor (GM-CSF) for the treatment of various inflammatory diseases; macrophage colony-stimulating factor (M-CSF) for the treatment of various inflammatory diseases; keratinocyte growth factor (KGF) for the treatment of epithelial tissue damage; chemokines such as monocyte chemoattractant protein-1 (MCP-1) for the treatment of recurrent miscarriage, HIV-related complications, and insulin resistance; tumor necrosis factor (TNF) and receptors for the treatment of various immune diseases; α1-antitrypsin for the treatment of emphysema or chronic obstructive pulmonary disease (COPD); mucopolysaccharidosis type I (MPS α-L-idronidase for the treatment of ornithine transcarbamoylase (OTC) deficiency; phenylalanine hydroxylase (PAH) or phenylalanine ammoniacal enzyme (PAL) for the treatment of phenylketonuria (PKU); lipoprotein lipase for the treatment of lipoprotein lipase deficiency; apolipoprotein (Apo) for the treatment of apolipoprotein (Apo) AI deficiency; low density lipoprotein receptor (LDL-R) for the treatment of familial hypercholesterolemia (FH); low albumin Albumin for the treatment of cystinemia;Lecithin cholesterol acyltransferase (LCAT);Carbamoyl synthetase I;Argininosuccinate synthase;Argininosuccinate lyase;Arginase;Fumarylacetoacetate hydrolase;Porphobilinogen deaminase;Cystathionine β-synthase for the treatment of homocystinuria;Branched-chain ketoacid decarboxylase;Isovaleryl-CoA dehydrogenase;Propionyl-CoA carboxylase;Methylmalonyl-CoA mutase;Glutaryl-CoA dehydrogenase;Insulin; pyruvate carboxylase; hepatic phosphorylase; phosphorylase kinase glycine decarboxylase; H protein; T protein; cystic fibrosis transmembrane conductance regulator (CFTR); ATP-binding cassette for the treatment of Stargardt disease, subfamily A (ABC1), member 4 (ABCA4); or dystrophin.

[0159] In further embodiments, the transgene encodes a protein for treating a disease or disorder selected from the group consisting of hereditary angioedema, Pompe disease, hemophilia A, hemophilia B, Fabry disease, wet macular degeneration, Leber's hereditary optic neuropathy, and Stargardt disease. III.E. Inhibitory Nucleic Acids

[0160] DNA vectors include short hairpin RNA (shRNA), small interfering RNA (siRNA), microRNA (miRNA), and RNA iA variety of different transgenes can be provided that encode a variety of different inhibitory nucleic acids, such as ribozymes, and antisense RNA. In different embodiments, the inhibitory nucleic acid binds to a gene, a transcript of a gene, or a transcript of a gene associated with a polynucleotide repeat disease selected from the group consisting of the huntingtin (HTT) gene, a gene associated with pyorrhagic alveolar atrophy (atrophin 1, ATN1), androgen receptor on the X chromosome in spinocerebellar atrophy, human Ataxin-1, -2, -3, -7, Cav2.1 P / Q voltage-gated calcium channel (CACNA1A), TATA binding protein, ataxin 8 opposite chain (ATXN8OS), serine / threonine protein phosphatase 2A in spinocerebellar ataxia (types 1, 2, 3, 6, 7, 8, 1217). 55 kDa regulatory subunit Bβ isoform, FMR1 (fragile X mental retardation 1) in fragile X syndrome, FMR1 (fragile X mental retardation 1) in fragile X-associated tremor / ataxia syndrome, FMR2 (fragile X mental retardation 2) or AF4 / FMR2 family member 2 in fragile XE mental retardation; myotonin protein kinase (MT-PK) in myotonic dystrophy; frataxin in Friedreich's ataxia; superoxide dismutase 1 (SOD1) gene variants in amyotrophic lateral sclerosis; genes involved in the development of Parkinson's disease and Alzheimer's disease; apolipoprotein B (APOB) and proprotein convertase subtilisin / kexin type 9 (PCSK9), hypercholesterolemia; HIV Tat, human immunodeficiency virus transactivator gene in HIV infection; HIV TAR, HIV TAR, transactivator response element gene of human immunodeficiency virus; CC chemokine receptor (CCR5) in HIV infection; Rous sarcoma virus (RSV) nucleocapsid protein in RSV infection, liver-specific microRNA (miR-122) in hepatitis C virus infection; p53, acute kidney injury or delayed kidney transplant or kidney failure; protein kinase N3 (PKN3) involved in the progression of recurrent or metastatic solid malignancies;LMP2, also known as proteasome subunit beta type 9 (PSMB 9), metastatic melanoma; LMP7, also known as proteasome subunit beta type 8 (PSMB 8), metastatic melanoma; LMP8, also known as proteasome subunit beta type 10 (PSMB 10), metastatic melanoma MECL1, metastatic melanoma; Vascular endothelial growth factor (VEGF) in solid tumors; Kinesin spindle proteins in solid tumors, Apoptosis inhibitor B-cell CLL / lymphoma (BCL-2) in chronic myeloid leukemia; Ribonucleotide reductase M2 (RRM2) in solid tumors; Furin in solid tumors; Polo-like kinase 1 (PLK1) in liver tumors, Diacylglycerol acyltransferase 1 (DGAT1) in hepatitis C infection, β-catenin in familial adenomatous polyposis; β2-adrenergic receptor, glaucoma; RTP801 / Redd1, also known as DNA damage-inducible transcript 4 protein, in diabetic macular edema (DME) or age-related macular degeneration; Vascular endothelial growth factor receptor I (VEGFR1) in age-related macular degeneration or choroidal neovascularization; Caspase 2 in non-arteritic ischemic optic neuropathy; Keratin 6A in congenital pachyonychia N17K mutant protein; influenza A virus genome / gene sequence in influenza infection; SARS coronavirus genome / gene sequence in severe acute respiratory syndrome (SARS) infection; respiratory syncytial virus genome / gene sequence in respiratory syncytial virus infection; Ebola filovirus genome / gene sequence in Ebola hemorrhagic fever infection; Hepatitis B virus genome / gene sequence in Hepatitis B and Hepatitis C infection; Herpes simplex virus (HSV) genome / gene sequence in HSV infection; Coxsackievirus B3 genome / gene sequence in Coxsackievirus B3 infection; silencing of disease-causing alleles (allele-specific silencing) of torsin A (TOR1A)-like genes in primary dystonia, pan-class I and HLA allele specificity in transplantation; and mutant rhodopsin gene (RHO) in autosomal dominant retinitis pigmentosa (adRP). III.F Gene Editing

[0161] The DNA vector can provide a variety of different transgenes encoding a variety of different gene editing nucleic acids, such as ZFN, TALEN, CRISPR-Cas9, etc. In different embodiments, the gene editing nucleic acid edits the DNA of a subject to provide a therapeutic protein, as provided in Section III.D. (supra), or to disrupt a gene, as provided in Section III.E. (supra). IV. Immune Cell Modulators

[0162] In some cases, administration of a DNA vector may cause an undesirable immune response, for example, due to the DNA vector components, the transgene product being recognized as foreign, or the edited gene producing a protein being considered foreign. In such cases, if desired, the host's immune response can be reduced, for example, using immune cell modulators or immunosuppressants. In some cases, such as cancer therapy, viral therapy, or bacterial therapy, a particular response may be advantageous. IV.A. Phagocytic Cell Reducers

[0163] "Phagocyte reducing agent" refers to an agent that reduces or destroys phagocytes in a subject and / or inhibits the function of one or more phagocytes. Phagocytes are also referred to herein as phagocytes, phagocytic immune cells, phagocytic cells, or phagocytic immune cells, and include macrophages, monocytes, neutrophils, and dendritic cells. Langerhans cells are dendritic cells found in the skin. Mast cells are found in many tissues, including the lungs and skin, and also function as phagocytes.

[0164] "Monocyte and / or macrophage reducing agent" refers to an agent that depletes or destroys monocytes and / or macrophages in a subject and / or inhibits one or more monocyte and / or macrophage functions. Monocyte and / or macrophage reducing agents can target monocytes and / or macrophages. Macrophages are mononuclear phagocytes that are differentiated monocytes. In different tissues, macrophages are called by different names. Examples of tissue-specific or resident macrophages include Kupffer cells in the liver, enteric macrophages in the intestine, microglial cells in the brain, alveolar macrophages in the lungs, resident macrophages in the kidneys, macrophages in the skin, red meat macrophages in the spleen, and osteoclasts in the bones. Examples of monocyte and / or macrophage reducing agents include agents that target phagocytic immune cell markers, e.g., CD115 inhibitors, such as anti-CD115 antibodies or CD115 small molecule inhibitors; F4 / 80 inhibitors, such as anti-F4 / 80 antibodies or F4 / 80 small molecule inhibitors; CD68 inhibitors, such as anti-CD68 antibodies or CD68 small molecule inhibitors; CD11b inhibitors, such as anti-CD11b antibodies or CD11b small molecule inhibitors; the chemotherapeutic agent trabectedin; intralipids; empty liposomes; and bisphosphonates, including clodronate. In certain embodiments, the monocyte and / or macrophage reducing agent is not clodronate. In certain embodiments, clodronate is used in combination with at least one additional monocyte and / or macrophage reducing agent.

[0165] "Neutrophil depleting agent" refers to an agent that reduces or destroys neutrophils in a subject and / or inhibits one or more neutrophil functions. Neutrophil depleting agents target neutrophils. Examples of neutrophil depleting agents include agents that target phagocytic immune cell markers, such as: Ly6G inhibitors, including anti-Ly6G antibodies or Ly6G small molecule inhibitors; CD177 inhibitors, including anti-CD177 antibodies or CD177 small molecule inhibitors; CD14 inhibitors, including anti-CD14 antibodies or CD14 small molecule inhibitors; CD15 inhibitors, including anti-CD15 antibodies or CD15 small molecule inhibitors; CD11b inhibitors, including anti-CD11b antibodies or CD11b small molecule inhibitors; CD16 inhibitors, including anti-CD16 antibodies or CD16 small molecule inhibitors; anti-CD32 antibodies or CD32 inhibitors. a CD32 inhibitor, including an anti-CD33 antibody or a CD33 small molecule inhibitor; a CD44 inhibitor, including an anti-CD44 antibody or a CD44 small molecule inhibitor; a CD45 inhibitor, including an anti-CD45 antibody or a CD45 small molecule inhibitor; a CD66b inhibitor, including an anti-CD66b antibody or a CD66b small molecule inhibitor; or a CD18 inhibitor, including an anti-CD18 antibody or a CD18 small molecule inhibitor; a CD62L inhibitor, including an anti-CD62L antibody or a CD62L small molecule inhibitor; and a Gr-1 inhibitor, including an anti-Gr-1 antibody or a Gr-1 small molecule inhibitor.

[0166] "Dendritic cell reducing agent" refers to an agent that depletes or destroys dendritic cells in a subject and / or inhibits the function of one or more dendritic cells. Dendritic cell reducing agents can target any dendritic cell. Examples of dendritic cell reducing agents include agents that target phagocytic immune cell markers, such as PDCA1 inhibitors, including anti-PDCA1 antibodies or small molecule PDCA1 inhibitors; and CD11c inhibitors, including anti-CD11c antibodies or small molecule CD11c inhibitors.

[0167] "Inhibitor" refers to any compound capable of downregulating, decreasing, reducing, suppressing, or inactivating the amount and / or activity of a target protein. Inhibitors can be proteins, oligopeptides, polypeptides, nucleic acids, genes, or chemical molecules. Suitable protein inhibitors include, for example, monoclonal and polyclonal antibodies that bind to the target protein, and small molecules.

[0168] Examples of CD115 inhibitors include: CD115 small molecule inhibitors pexidartinib (PLX-3397), BLZ-945, linifanib (ABT-869), JNJ-28312141 (Johnson & Johnson), JNJ-40346527 (Johnson & Johnson), PLX7486 (Plexxikon), ARRY-382 (Array BioPharma), anti-CD115 antibodies such as: AFS98 (Invitrogen or BioCell), 12-3A3-1B10 (Invitrogen), 6C7 (Bio-S), Cabiralizumab (FPA008), 25949-1-AP (Proteintech), 1G4 (Abnova), 3G12 (Abnova), 604B5 2E11 (Invitrogen), Emactuzumab (RG-7155; Roche), AMG 820 (Amgen), IMC-CS4, and ROS8G11 (Invitrogen). In certain embodiments, the antibody or antigen-binding fragment thereof is AFS98 (e.g., BioCell BE0213 and Oncogene 1995;11(12):2469-2476).

[0169] In view of the present disclosure, any suitable Ly6G inhibitor can be used, including those known to those of skill in the art. Examples of anti-Ly6G antibodies include A8 (BioCell BP0075-1) and RB6-8C5 (ab25377).

[0170] Intralipids and empty liposomes have been shown to inhibit one or more functions of monocytes and macrophages. See, for example, Liu et al., Biochim Biophys Acta. 2013 Jun;1830(6):3447-53 and Saunders et al., Nano Lett. 2020 Jun 10;20(6):4264-4269. Pretreatment with Intralipids or empty liposomes can effectively saturate monocyte / macrophage cells and prevent phagocytosis of non-viral therapeutics. Examples of Intralipids and empty liposomes include I141-100ML (Sigma Aldrich), 2B6063 (Baxter), and those described in Liu et al., Biochim Biophys Acta. 2013 Jun;1830(6):3447-53 and Saunders et al., Nano Lett. 2020 Jun 10;20(6):4264-4269.

[0171] Examples of bisphosphonates include clodronic acid, pamidronate, ibandronate, alendronate, and zoledronate.

[0172] Other examples of "phagocytic cell reducing agents" include palbociclib (Ibrance®; Pfizer) and cromolyn sodium (Nasalcrom®; Bausch + Lomb). IV.B. Immunosuppressants

[0173] Immunosuppressants are compounds capable of reducing or halting the activity of a subject's immune system. A variety of immune responses are produced, including innate and humoral immune responses. For example, immune responses include detectable changes in activation of Toll receptors, expression and / or secretion of lymphokines (e.g., cytokines or chemokines), activation of macrophages, activation of dendritic cells, activation of T cells (e.g., CD4+ or CD8+ T cells), activation of NK cells, and / or activation of B cells (e.g., production and / or secretion of antibodies). Other examples of immune responses include: binding of an immunogen (such as an antigen) to an MHC molecule and induction of a cytotoxic T lymphocyte ("CTL") response, a B cell response (e.g., antibody production), and / or a T helper lymphocyte response, and / or a delayed type hypersensitivity (DTH) response to the antigen from which the immunogenic polypeptide is derived, induction of proliferation of cells of the immune system, and increased processing and presentation of antigens by antigen-presenting cells.

[0174] Examples of immunosuppressants include: calcineurin inhibitors such as cyclosporine, ISA(TX)247, tacrolimus or calcineurin; rapamycin targeted drugs such as sirolimus, everolimus, FK778, TAFA-93; interleukin-2α chain blockers such as basiliximab or daclizumab; inosine monophosphate dehydrogenase inhibitors such as mycophenolate mofetil; dihydrofolate reductase inhibitors such as methotrexate; immunosuppressive antimetabolites such as azathioprine; JAK inhibitors such as ruxolitinib; cytokine inhibitors such as anti-cytokine antibodies, e.g., siltuximab; or steroids.

[0175] In certain embodiments, the immunosuppressant is an anti-inflammatory agent.In certain embodiments, the immunosuppressant is a steroid, such as a corticosteroid, prednisone, prednisolone, cyclosporine (e.g., cyclosporine A), mycophenolate; a B cell targeting antibody, such as rituximab; a proteasome inhibitor, such as bortezomib; a mammalian target of rapamycin (mTOR) inhibitor, such as rapamycin; a tyrosine kinase inhibitor, such as ibrutinib; an inhibitor of B cell activating factor (BAFF); or an inhibitor of proliferation-inducing ligand (APRIL) or its derivatives.In certain embodiments, the immunosuppressant is an anti-IL-1β agent (e.g., anti-IL-1β monoclonal antibody canakinumab (Ilaris®)) or an anti-IL-6 agent (e.g., anti-IL-6 antibody sirukumab or anti-IL-6 receptor antibody tocilizumab (Actemra®)), or a combination thereof.

[0176] The term "steroid" refers to chemical compounds that contain three cyclohexane rings and one cyclopentane ring. The rings are arranged to form a tetracyclic cyclopentaphenanthrene, or gonan. There are various types of steroids, including corticosteroids and glucocorticosteroids.

[0177] The term "corticosteroid" refers to a group of steroid hormones produced in the adrenal cortex or synthetically produced. In certain embodiments, the steroid can be a corticosteroid. Corticosteroids are involved in a wide range of physiological systems, including stress response, immune response, control of inflammation, carbohydrate metabolism, protein catabolism, blood electrolyte levels, and behavior. Corticosteroids are generally classified into four classes based on chemical structure. Group A corticosteroids (short- to medium-acting glucocorticoids) include hydrocortisone, hydrocortisone acetate, cortisone acetate, tixocortol pivalate, prednisolone, methylprednisolone, and prednisone. Group B corticosteroids include triamcinolone acetonide, triamcinolone alcohol, mometasone, amcinonide, budesonide, desonide, fluocinonide, fluorocinolone acetonide, and halcinonide. Class C corticosteroids include betamethasone, betamethasone sodium phosphate, dexamethasone, dexamethasone sodium phosphate, and fluocortolone. Class D corticosteroids include hydrocortisone 17-butyrate, hydrocortisone-17-valerate, aclometasone dipropionate, betamethasone divalerate, betamethasone dipropionate, prednicarb acid, clobetasone 17-butyrate, clobetasol 17-propionate, fluocortolone caproate, fluocortolone pivalate, and fluprednidene acetate.Non-limiting examples of corticosteroids include: aldosterone, beclomethasone, beclomethasone dipropionate, betamethasone, betamethasone-21-phosphate disodium, betamethasone valerate, budesonide, clobetasol, clobetasol propionate, clobetasone butyrate, clocortolone pivalate, cortisol, cortisterone, cortisone, deflazacort, dexamethasone, dexamethasone acetate, dexamethasone sodium phosphate, diflorasone diacetate, dihydroxycortisone, flucinonide, fludocorthol acetate. Dihydrocortisone, flumethasone, flunisolide, flucionolone acetonide, fluticasone frurate, fluticasone propionate, halcinonide, halbutasone, hydrocortisone, hydrocortisone acetate, hydrocortisone succinate, 16α-hydroxyprednisolone, isoflupredone acetate, medrysone, methylprednisolone, prednacinolone, predlicarbate, prednisolone, prednisolone acetate, prednisolone sodium succinate, prednine, triamcinolone, triamcinolone, triamcinolone diacetate.

[0178] Corticosteroids come in a variety of generic and brand-name forms: CORTONE TM ACETATE TM ,ADRESON TM ,ALTENSIONA TM ,CORTELANT TM ,CORTISTAB TM ,CORTISIL TM ,CORTOGEN TM ,CORTONE TM ,SCHEROSON TM );Dexamethasone oral preparation (DECADRON ORAL TM , DEXAMETH TM , DEXONE TM , HEXADROL-ORAL TM , DEXAMETHASONE TM INTENSOL TM , DEXONE 0.5 TM , DEXONE 0.75TM , DEXONE 1.5 TM , DEXONE 4 TM );Hydrocortisone oral preparation (CORTEF TM ,HYDROCORTONE TM ); Hydrocortisone cypionate (CORTEF ORAL SUSPENSION TM ); Methylprednisolone oral preparation (MEDROL-ORAL TM ); Prednisolone oral preparation (PRELONE TM ,DELTA-CORTEF TM ,PEDIAPRED TM ,ADNISOLONE TM ,CORTALONE TM ,DELTACORTRIL TM ,DELTASOLONE TM ,DELTASTAB TM ,DI-ADRESON F TM ,ENCORTOLONE TM ,HYDROCORTANCYL TM ,MEDISOLONE TM ,METICORTELONE TM ,OPREDSONE TM ,PANAAFCORTELONE TM ,PRECORTISYL TM ,PRENISOLONA TM ,SCHERISOLONA TM ,SCHERISOLONE TM );Prednisone (DELTASONE TM ,LIQUID PRED TM ,METICORTENT TM ,ORASONE 1 TM ,ORASONE 5 TM ,ORASONE 10 TM ,ORASONE 20 TM ,ORASONE 50 TM ,PREDNICEN-M TM ,PREDNISONE INTENSOL TM ,STERA PRED TM ,STERAPRED DS TM,ADASONE TM ,CARTANCYL TM ,COLISONE TM ,CORDROL TM ,CORTAN TM ,DACORTIN TM ,DECORTIN TM ,DECORTISYL TM ,DELCORTIN TM ,DELLACORT TM ,DELTADOME TM ,DELTACORTENE TM ,DELTISONA TM ,DIADRESON TM ,ECONOSONE TM ,ENCORTON TM ,FERNISONE TM ,NISONA TM ,NOVOPREDNISONE TM ,PANAFCORT TM ,PANASOL TM ,PARACORT TM ,PARMENISON TM ,PEHACORT TM ,PREDELTIN TM ,PREDNICORT TM ,PREDNICOT TM ,PREDNIDIB TM ,PREDNIMENT TM ,RECTODELT TM ,ULTRACORTEN TM ,WINPRED TM ); Triamcinolone Oral Preparation (KENACORT TM ,ARISTOCORT TM ,ATOLONE TM ,SHOLOG A TM ,TRAMACORT-D TM ,TRI-MED TM ,TRIAMCOT TM ,TRISTOPLEX TM ,TRYLONE D TM ,U-TRI-LONE TMIn certain embodiments, the corticosteroid is: dexamethasone, prednisone, prednisolone, triamcinolone, clobetasol propionate, betamethasone valerate, betamethasone dipropionate, or mometasone furoate. Methods for synthesizing steroids and corticosteroids are well known in the art, and many are commercially available.

[0179] Corticosteroids, such as dexamethasone, can be delivered as free dexamethasone, as a separate LNP composition, or as part of the same LNP composition as DNA. Chen et al., Journal of Controlled Release 2018, 286, 46-54, describe LNPs that provide nucleic acids linked to fatty acids and dexamethasone. V. Pharmaceutical Compositions

[0180] A pharmaceutical composition comprises one or more active ingredients together with a pharma- ceutically acceptable carrier. "Pharmaceutically" or "pharmaceutical acceptable" refers to a non-toxic molecular entity suitable for administration and / or storage. Pharmaceutical compositions can include multiple therapeutically active agents. Examples of pharma- ceutically acceptable carriers include (in the amounts used) non-toxic solid, semi-solid or liquid fillers, diluents, encapsulating materials or formulations.

[0181] The form of the pharmaceutical composition, the route of administration, the dosage, and the regimen will of course depend on the condition being treated, the severity of the disease, the age, weight, and sex of the patient, etc. Pharmaceutical compositions for the agents described herein can be formulated for topical, oral, nasal, parenteral, intraocular, intravenous, intramuscular, or subcutaneous administration.

[0182] In one embodiment, the pharmaceutical composition comprises a formulation that can be injected into a subject. Examples of components of the formulation for injection include isotonicity agent, sterility, saline (e.g., monosodium or disodium phosphate, sodium chloride, potassium chloride, calcium chloride or magnesium chloride, and mixtures of these salts), buffered saline, sugar (e.g., glucose), and water for injection. The pharmaceutical composition includes a dry product, for example, a lyophilized composition, and can be optionally added with sterile water or saline to constitute a solution for injection. The dosage used for administration can be adapted as a function of various parameters, for example, the mode of administration, the pathology involved, and / or the desired duration of treatment.

[0183] Other pharma- ceutically acceptable forms include tablets or other solid forms for oral administration, including time-release capsules.

[0184] A pharmaceutical composition comprising a DNA vector containing a therapeutic transgene can be administered to a subject in a dosage suitable for treating a particular disease or disorder. In different embodiments, a suitable dosage can be about 0.01 mg / kg to about 10 mg / kg of vector per kg of subject's body weight, about 0.01 mg / kg to about 0.1 mg / kg of vector per kg of subject's body weight, about 0.1 mg / kg to about 1.0 mg / kg of vector per kg of subject's body weight, and about 1.0 mg / kg to about 10 mg / kg of vector per kg of subject's body weight.

[0185] The small molecule cytoplasmic DNA sensing inhibitor or immune cell modulator inhibitor can be administered to a subject in a dosage appropriate for the particular disease or disorder. In different embodiments, the suitable dosage can be about 0.1 mg / kg to about 100 mg / kg, about 0.1 mg / kg to about 1 mg / kg, about 1.0 mg / kg to about 10 mg / kg, and about 10.0 mg / kg to about 100 mg / kg of the subject's body weight.

[0186] Antibodies targeting phagocytic immune cell markers can be administered to a subject at any suitable dose. For example, a suitable dose can be from about 0.01 mg / kg to about 5 mg / kg of body weight of a subject, with the dose being administered in a total of 1 to 10 injections.

[0187] CD115 inhibitors such as pexidartinib can be administered to subjects at appropriate doses.For example, suitable doses can be about 0.1mg / kg to about 100mg / kg, about 0.1mg / kg to about 1mg / kg, about 1.0mg / kg to about 10mg / kg, and about 10.0mg / kg to about 100mg / kg of the subject's body weight.

[0188] The bisphosphonate, e.g., clodronic acid, can be administered to a subject in any suitable dose. For example, suitable dosages can be from about 0.1 mg / kg to about 100 mg / kg, from about 0.1 mg / kg to about 1 mg / kg, from about 1.0 mg / kg to about 10 mg / kg, and from about 10.0 mg / kg to about 100 mg / kg of the subject's body weight.

[0189] The corticosteroid, such as dexamethasone, can be administered to the subject in any suitable dose. For example, suitable dosages can be about 0.1 mg / kg to about 100 mg / kg, about 0.1 mg / kg to about 1 mg / kg, about 1.0 mg / kg to about 10 mg / kg, and about 10.0 mg / kg to about 100 mg / kg of the subject's body weight.

[0190] VI. Administration and Treatment

[0191] The different compounds and compositions described herein can be administered to a subject for different purposes, including research purposes and treatment of a mammalian disease or disorder, with a preferred use being the treatment of a human disease.

[0192] "Treatment" or "treatment" refers to both preventative and therapeutic treatment of a patient with a disease or disorder. "Preventative" treatment refers to reducing the likelihood of contracting a disease or disorder or reducing the severity of the disease or disorder. "Therapeutic" refers to a clinically meaningful improvement in at least one symptom or cause associated with a disease or disorder. Thus, treatment includes administration to subjects at risk of contracting a disease or disorder, subjects suspected of having a disease or disorder, as well as subjects suffering from or diagnosed with a disease or disorder, including the suppression of clinical recurrence.

[0193] The terms "ameliorate" and "amelioration" refer to a detectable or measurable improvement in the symptoms of a disease or disorder, or in the underlying cellular response. Detectable or measurable improvement includes subjective or objective reduction, alleviation, suppression, limitation or control in the occurrence, frequency, severity, progression or duration of a disease or disorder, or a complication resulting from or associated with a disease or disorder, or amelioration of a symptom or underlying cause or consequence of a disease or disorder, or reversal of a disease or disorder. In the case of Pompe, an effective amount includes an amount that inhibits or reduces glycogen production or accumulation, promotes or increases glycogen breakdown or removal, and improves muscle tone and / or strength and / or respiratory function. In the case of HemA or HemB, an effective amount includes an amount that reduces the frequency or severity of acute bleeding episodes in a subject, and reduces clotting time as measured by a clotting assay.

[0194] The terms "effective amount" and "sufficient amount" refer to an amount necessary to obtain a desired effect. Treatment can be performed by administering a therapeutically effective amount of a DNA vector to a subject. To obtain a therapeutic or prophylactic effect, a therapeutically effective amount can be administered in a single dose or multiple doses.

[0195] Other agents may be administered in an "effective amount" or "sufficient amount" to achieve a desired effect. As an example, an effective amount of a DNA sensing inhibitor is an amount provided in a single or multiple doses that inhibits the activity of the cGAS-STING pathway or the inflammasome pathway, resulting in a decrease in one or more activities of the innate immune response. Similarly, an effective amount of an immune cell regulator is an amount provided in a single or multiple doses that provides a detectable decrease in phagocytes and / or phagocyte function, for example, as provided in Section IV.A.; an effective amount of an immunosuppressant is an amount provided in a single or multiple doses that inhibits immune system activity, for example, as provided in Section IV.B.

[0196] An effective amount can be administered alone or in combination with another composition, therapy, protocol, or treatment regimen, and the amount can be proportionally increased based on, for example, the needs of the subject, the type, condition, and severity of the disease or disorder being treated, or side effects.

[0197] An effective amount or a sufficient amount does not necessarily have to be effective in each subject treated, nor does it have to be effective in the majority of subjects treated in a given group or population.An effective amount or a sufficient amount means effectiveness or sufficiency in a particular subject, not effectiveness or sufficiency in a group or the general population.Typical examples of such methods are that some subjects respond more, some less, or even not at all to a certain treatment method or use.

[0198] When the DNA vector and the cytoplasmic DNA sensing inhibitor are administered separately, they can be administered in any order or at about the same time, hi certain embodiments, the inhibitor is administered at least 60 minutes, at least 90 minutes, or at least 120 minutes before the DNA vector.

[0199] In certain embodiments, the cytoplasmic DNA sensing inhibitor is administered at about the same time, up to about 5 minutes, up to about 15 minutes, up to about 30 minutes, up to about 45 minutes, up to about 60 minutes, up to about 90 minutes, up to about 2 hours, up to about 3 hours, up to about 4 hours, up to about 5 hours, up to about 6 hours, up to about 7 hours, up to about 8 hours, up to about 9 hours, up to about 10 hours, up to about 12 hours, up to about 1 day, up to about 2 days, up to about 3 days, up to about 4 days, or up to about 1 week before the administration of the DNA vector. Preferably, the cytoplasmic DNA sensing inhibitor is administered at about the same time, up to about 5 minutes, up to about 15 minutes, up to about 30 minutes, up to about 45 minutes, up to about 60 minutes, up to about 90 minutes, up to about 2 hours, up to about 3 hours, or up to about 4 hours before the administration of the DNA vector. In certain embodiments, the cytoplasmic DNA sensing inhibitor is administered about 15 minutes, about 30 minutes, about 45 minutes, about 60 minutes, about 90 minutes, about 120 minutes, or about 1 day after the DNA.

[0200] In certain embodiments, the cytoplasmic DNA sensing inhibitor is administered about simultaneously, about 5 minutes, about 10 minutes, about 15 minutes, about 30 minutes, about 45 minutes, about 60 minutes, about 90 minutes, 2 hours, about 2.5 hours, about 3 hours, about 3.5 hours, or about 4 hours prior to administration of the DNA vector.

[0201] The DNA vector and the cytoplasmic DNA-sensing inhibitor can be provided in the same nanoparticle for approximately simultaneous release, or the nanoparticle can be designed to delay the release of one of the components, hi one embodiment, the nanoparticle is designed to release the inhibitor prior to release of the DNA.

[0202] The therapeutic dosage of the DNA vector may vary and depends on the type, onset, progression, severity, frequency, duration, or probability of the disease or disorder for which treatment is intended, the desired clinical endpoint, previous or concurrent treatment, the general health, age, sex, race, or immunological competence of the subject, and other factors that would be understood by one of skill in the art. The dosage, number of doses, frequency of administration, or duration of administration may be proportionally increased or decreased depending on the side effects of the treatment or therapy, complications, or other risk factors, and the condition of the subject.

[0203] Dosages to achieve a therapeutic effect, e.g., DNA vector dosages in milligrams per kilogram of body weight (mg / kg), will also vary based on several factors, such as the route of administration, the level of transgene expression required to achieve a therapeutic effect, the particular disease or disorder being treated, the host immune response to the DNA, the host immune response transgene expression product, the stability of the expressed protein, peptide or nucleic acid, etc. Based on the guidance provided herein, one of skill in the art will be able to determine the appropriate dosage range of the DNA vector for treating a patient with a particular disease or disorder.

[0204] The overall expression level of the transgene may vary depending on the use of the DNA vector. In different embodiments of gene therapy to provide a therapeutic protein, the expression or activity provided is at least 1%, at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 100% of the normal expression of the corresponding target protein.

[0205] In certain embodiments, the method according to the invention may result in a reduction in the expression or activity of the protein targeted by the therapeutic nucleic acid. In different embodiments, the reduction in expression or activity of the protein targeted by the therapeutic nucleic acid is at least 1%, at least 5%, at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 100% of the normal expression of the target protein.

[0206] The methods and uses of the present invention include systemic, local or topical delivery and administration, for example by injection or infusion. Direct delivery of pharmaceutical compositions in vivo can generally be achieved by injection using a conventional syringe, but other delivery methods, such as convection-enhanced delivery, are also envisioned (see, for example, U.S. Pat. No. 5,720,720). For example, the compositions can be delivered subcutaneously, intraepidermally, intradermally, intrathecally, intraorbitally, intramucosally, intraperitoneally (IP), intravenously (IV), intrapleurally, intraarterially, orally, intrahepatically, via the portal vein, or intramuscularly. Other administration methods include oral administration, pulmonary administration, suppositories, and transdermal formulations. VI.A. Illustrative Diseases and Disorders

[0207] Diseases and disorders that can be treated include: pulmonary diseases (e.g. cystic fibrosis), blood disorders (e.g. anemia), CNS diseases and disorders, epilepsy, lysosomal storage diseases (e.g. aspartylglucosaminuria), Batten disease, late infantile neuronal ceroid lipofuscinosis type 2 (CLN2), cystinosis, Fabry disease, Gaucher disease types I, II, and III, glycogen storage disease type II (Pompe disease), GM2-gangliosidosis type I (Tay-Sachs disease), GM2-gangliosidosis type II (Sandhoff disease), mucolipidosis type I (sialidosis types I and II), and type II ( I-cell disease), III (pseudo-Hurler disease), IV, mucopolysaccharide storage diseases (Hurler disease and variants, Hunter disease, Sanfilippo types A, B, C, D, Morquio types A, B, Maroteaux-Lamy disease, Sly disease), Niemann-Pick disease types A / B, C1, C2, Schindler disease types I and II, hereditary angioedema (HAE), copper or iron storage disorders (such as Wilson disease and Menkes disease), lysosomal acid lipase deficiency, neurological or neurodegenerative diseases, cancer, type 1 or type 2 diabetes, adenosine deaminase deficiency, metabolic disorders (e.g., glycogen storage diseases), and diseases of solid organs (such as the brain, liver, kidneys, and heart).

[0208] Glycogen storage disease type II (also called Pompe disease) can be treated with the methods according to the invention. Pompe disease is an autosomal recessive disorder caused by mutations in the gene encoding the lysosomal enzyme acid alpha-glucosidase (GAA), which catalyzes the breakdown of glycogen. The resulting enzyme deficiency leads to pathological accumulation of glycogen and alterations in the lysosomes, causing cardiac, respiratory and skeletal muscle dysfunction.

[0209] Treatable blood clotting disorders include hemophilia A, hemophilia A with inhibitory antibodies, hemophilia B, hemophilia B with inhibitory antibodies, deficiency of clotting factors VII, VIII, IX, X, XI, V, XII or II, von Willebrand factor deficiency or combined FV / FVIII deficiency, thalassemia, vitamin K epoxide reductase C1 deficiency, or gamma-carboxylase deficiency.

[0210] Other treatable diseases and disorders include those with trauma, injury, thrombosis, thrombocytopenia, stroke, coagulation disorders, bleeding associated with disseminated intravascular coagulation (DIC), excessive anticoagulation associated with heparin, low molecular weight heparins, pentasaccharides, warfarin, small molecule antithrombotic agents (e.g., FXa inhibitors), or platelet disorders such as Bernard Soulier syndrome, Glanzmann thrombasthenia, and storage pool deficiencies.

[0211] Other diseases and disorders that can be treated include proliferative diseases (e.g. cancer, tumors, dysplasias), metabolic diseases such as Crigler-Najjar and metabolic diseases of the liver; Friedreich's ataxia; infectious diseases; viral diseases induced, for example, by hepatitis B or C viruses, HIV, herpes, retroviruses, etc.; genetic diseases such as cystic fibrosis, dystroglycanopathy, myopathies such as Duchenne myomyopathies and dystrophies, myotubular myopathies, sickle cell anemia, sickle cell disease, Fanconi anemia, diabetes mellitus, and rheumatoid arthritis. Motor neuron diseases such as amyotrophic lateral sclerosis (ALS), myotubular myopathy, spinal muscular atrophy (SMA), spinobulbar muscular atrophy, or Charcot-Marie-Tooth disease; arthritis; severe combined immunodeficiencies such as RS-SCID, ADA-SCID, and X-SCID; Wiskott-Aldrich syndrome; X-linked thrombocytopenia; X-linked congenital neutropenia; chronic granulomatous disease; coagulation factor deficiencies; cardiovascular diseases such as restenosis, ischemia, dyslipidemia, and homozygous familial hypercholesterolemia; eye diseases such as retinitis pigmentosa, X-linked retinitis pigmentosa, autosomal dominant retinitis pigmentosa, recessive retinitis pigmentosa, choroideremia, choroideremia, choroideremia, rotator atrophy, retinochalasia, X-linked retinochalasia, macular degeneration, diabetic macular edema (DME), diabetic retinopathy with DME, wet age-related macular degeneration (wet age-related macular degeneration), and retinal degeneration. AMD or wAMD), macular edema after retinal vein occlusion, non-arteritic ischemic optic neuropathy, Leber's congenital amaurosis, Leber's hereditary optic neuropathy, color blindness, and Stargardt disease; lysosomal storage diseases such as Sanfilippo syndrome; hyperbilirubinemia such as CN types I and II and Gilbert syndrome; glycogen storage diseases such as GSDI, GSDII (Pompe disease), GSDIII, GSDIV, GSDV, GSDVI, GSDVII, GSDVIII, or fatal congenital cardiac glycogen storage disease.

[0212] In certain embodiments, the subject has a disease or disorder that affects or originates from the central nervous system (CNS). In certain embodiments, the disease is a neurodegenerative disease. Non-limiting examples of CNS or neurodegenerative diseases include Alzheimer's disease, Huntington's disease, ALS, hereditary spastic hemiplegia, primary lateral sclerosis, spinal muscular atrophy, Kennedy's disease, polyglutamine repeat disease, or Parkinson's disease. In certain embodiments, the disease is psychiatric disease, addiction (e.g., tobacco, alcohol, or drugs), epilepsy, Canavan's disease, or adrenoleukodystrophy. In certain embodiments, the CNS or neurodegenerative disease is a polyglutamine repeat disease, such as spinocerebellar ataxia (SCA1, SCA2, SCA3, SCA6, SCA7, or SCA17). VI.B. Examples of Administration for Various Diseases and Conditions

[0213] A wide variety of diseases and disorders can be treated based on the present application. This section focuses on administration for specific diseases or disorders. The examples provided, as well as other examples in this application, are intended to provide different embodiments and illustrative purposes.

[0214] In the case of Pompe disease, an effective amount is an amount of GAA that inhibits or reduces glycogen production or accumulation, promotes or increases glycogen breakdown or removal, reduces lysosomal changes in the subject's tissue, or improves muscle tone and / or strength and / or respiratory function in the subject. An effective amount can be determined, for example, by determining the kinetics of GAA uptake by myoblasts from plasma. The rate of GAA uptake (K uptake) in myoblasts appears to be effective at about 141 to 147 nM (e.g., Maga et al., J. Biol. Chem. 2012, 8; 288(3), 1428). In animal models, therapeutic effects have been observed at plasma GAA activity levels of about 1,000 nmol / hr / mL or higher, for example, about 1,000 to about 2,000 nmol / hr / mL.

[0215] For HemA and HemB, it is generally expected that a blood clotting factor concentration greater than 1% of the factor concentration found in normal individuals is required to change the severe disease phenotype to moderate. The severe phenotype is characterized by joint damage and life-threatening bleeding. A blood clotting factor concentration greater than 5% of normal is expected to be required to change the moderate phenotype to a mild phenotype.

[0216] Normal values ​​for FVIII are approximately 100-200 ng / ml and FIX levels in normal humans are 5000 ng / ml, although levels higher or lower are considered normal due to functional coagulation as determined by activated partial thromboplastin time (aPTT) one-stage clotting assays, etc. Thus, a therapeutic effect can be achieved such that the total amount of FVIII or FIX in a subject / human is greater than 1% of the FVIII or FIX present in a normal subject / human (e.g., 1% of 100-300 ng / mL). VI.C. Immune Response Considerations

[0217] Immune cell modulators and cytoplasmic DNA sensing inhibitors can be used to reduce the innate immune response mediated by the cGAS-STING and inflammasome pathways, as well as transgene expression products. For example, activation of the cGAS-STING pathway induces the production of interferons, proinflammatory cytokines, and proinflammatory chemokines such as IL-6, IFN-γ, IFN-β, CCL4, CCL5, and CXCL10, causing deleterious effects such as inflammation and cell death. Activation of the inflammasome pathway produces proinflammatory cytokines such as IL-1β, IL-18, and IL-33, causing deleterious effects such as inflammation and pyroptosis.

[0218] Administration of the DNA vector should minimize or eliminate the occurrence of an "undesirable immune response." The undesirable immune response induced by the DNA is distinct from the desirable immune response in a subject induced by an antigen (e.g., a bacterium or virus), if encoded by the vector.

[0219] In different embodiments, a safe or therapeutically acceptable immune response relates to the level of immune response in a subject following administration of DNA, as determined by inflammation, cytokine release, inflammasome activation, and inhibition of pyroptosis.

[0220] In certain embodiments, the methods described herein reduce the incidence of toxic cytokine release or "cytokine release syndrome" (CRS) or "severe cytokine release syndrome" (sCRS) or "cytokine storm"; or pyroptosis, which may occur in a subject.

[0221] Reducing toxic cytokine release or toxic cytokine levels includes reducing or inhibiting the production of toxic cytokine levels in a subject, or inhibiting or reducing the occurrence of cytokine release syndrome or cytokine storm in a subject. In certain embodiments, the toxic cytokine comprises a proinflammatory cytokine. In certain embodiments, the proinflammatory cytokine comprises IL-6, IFN-γ, IL-1β, or TNF-α, or any combination thereof.

[0222] In certain embodiments, cytokine release syndrome is characterized by elevated levels of several inflammatory cytokines and adverse physical responses in the subject, such as low blood pressure, high fever, shivering, etc. In certain embodiments, CRS is characterized by elevated levels of IL-6, IFN-γ, IL-1β, or TNF-α, or combinations thereof.

[0223] In certain embodiments, the measurement of cytokine level or concentration as an indicator of cytokine storm or pyroptosis can be expressed as fold increase, percentage (%) increase, net increase, or rate of change of cytokine level or concentration.In certain embodiments, absolute cytokine level or concentration at or above a certain level can be an indicator of the subject experiencing or about to experience cytokine storm.In certain embodiments, absolute cytokine level or concentration at a certain level or concentration, for example, the level or concentration that is normally found in the control subject that has not undergone non-viral gene therapy, can be an indicator of the method of inhibiting or reducing the occurrence of cytokine storm in the subject undergoing gene therapy.

[0224] The term "cytokine level" may include a concentration measure, a fold change measure, a percent (%) change measure, or a rate change measure. Additionally, methods for measuring cytokines in blood, saliva, serum, urine, plasma are well known in the art.

[0225] In certain embodiments, IFN-γ levels can be used as an indicator of cytokine storm and / or as a common indicator of the effectiveness of treatment against cytokine storm. In certain embodiments, IL-6 levels can be used as a common measure of cytokine storm and / or as a common measure of the effectiveness of treatment against cytokine storm. Other cytokines can also be used as markers of cytokine storm, such as TNF-α, IB-1α, IL-8, IL-13, etc.

[0226] In certain embodiments, IL-18 is used as an indicator of pyroptosis and / or as an indicator of the effectiveness of a treatment against pyroptosis.

[0227] The level of cytokines in the subject can be analyzed, measured or determined before and / or after administration of DNA. The level of cytokines in the subject can be analyzed or measured multiple times before and / or after administration of DNA. Exemplary methods for analyzing and measuring cytokine levels in biological samples include mesoscale delivery platforms (MSD).

[0228] The immune cell modulating agent described in section IV can be administered before, during, or after administration of the DNA vector or the cytoplasmic DNA sensing inhibitor. In different embodiments, the immune cell modulating agent is administered about 1 minute to about 1 hour, about 2 hours, about 3 hours, or about 4 hours before administration of the DNA vector containing the transgene and the pharma- ceutically acceptable carrier. In different embodiments, the DNA vector is administered about 1 minute to about 1 hour, 2 hours, 3 hours, or 4 hours before the immune cell modulating agent. In different embodiments, the immune cell modulating agent is administered at least one day before the DNA vector, optionally up to one year before the DNA vector, for example, at or below 52 weeks, 51 weeks, 50 weeks, 49 weeks, 48 ​​weeks, 47 weeks, 46 weeks, 45 weeks, 44 weeks, 43 weeks, 42 weeks, 41 weeks, 40 weeks, 39 weeks, 38 weeks, 37 weeks, 36 weeks, 35 weeks, 34 weeks, 33 weeks, 32 weeks, 31 weeks, 30 weeks, 29 weeks, 28 weeks, 27 weeks, or less. The DNA vector may be administered up to 1 week, 26 weeks, 25 weeks, 24 weeks, 23 weeks, 22 weeks, 21 weeks, 20 weeks, 19 weeks, 18 weeks, 17 weeks, 16 weeks, 15 weeks, 14 weeks, 13 weeks, 12 weeks, 11 weeks, 10 weeks, 9 weeks, 8 weeks, 7 weeks, 6 weeks, 5 weeks, 4 weeks, 3 weeks, 2 weeks, 1 week, 6 days, 5 days, 4 days, 3 days, or 2 days before the DNA vector, optionally administered up to 1 week, 2 weeks, 3 weeks, 4 weeks before the DNA vector.

[0229] In certain embodiments, the bisphosphonate and / or immune cell modulating agent is contained within a nanoparticle that includes DNA, e.g., encapsulated within a LNP, LPNP, polymeric nanoparticle, protein-based nanoparticle, or peptide cage. VI.D. Combination Therapy

[0230] The DNA vectors described herein can be used in combination with other treatments for a particular disease or disorder. VI.E. Kit

[0231] Further provided herein is a kit providing in separate containers at least (a) a pharmaceutical composition comprising nanoparticles comprising DNA; (b) a cytoplasmic DNA sensing inhibitor selected from the group consisting of a cGAS-STING pathway inhibitor and an inflammasome pathway inhibitor; and (c) an optional immune cell modulating agent. In different aspects and embodiments, the DNA and cytoplasmic DNA sensing inhibitor are as described in any of the first, second, third, and fourth aspects and related embodiments; and the immune cell modulating agent is as described throughout Section IV (supra). The amounts of the different components can be readily determined based on the guidance provided herein, including throughout Sections V. and VI., supra. The kit can also provide a label with instructions for administration according to the methods described herein.

[0232] Although many different aspects and embodiments of the present invention have been described throughout this application, those skilled in the art may nonetheless make various changes and modifications to adapt the present invention to various usages and conditions without departing from the spirit and scope of the present invention. EXAMPLES

[0233] The following further illustrates different features of the invention and methodologies for practicing the invention. The examples provided do not limit the claimed invention. Example 1: Inhibition of DNA-LNP-Induced IRF Activation by H-151 In Vitro

[0234] THP1-Dual TMCells (InvivoGen) were seeded at a density of 45,000 cells / well in 96-well plates. After overnight culture, cells were treated with 25 ng of DNA-LNP / well in the presence of 0, 0.2 or 2.1 ng of the small molecule STING inhibitor H-151 (InvivoGen). H-151 was either a) co-encapsulated with DNA in the LNPs or b) provided in a soluble form. After 24 h of culture, activation of the interferon regulatory factor (IRF) pathway ("fold IRF activity") was determined by measuring the luminescent signal (lucia luciferase) in the cell culture supernatant. DNA-LNPs were composed of (1) a DNA plasmid (a nanoplasmid expression cassette encoding human coagulation factor IX (hFIX)) and (2) Lipid5 (Sabnis et al., IA, described further below), 50%; C14-PEG2000, 1.5%; cholesterol, 38.5%; and DSPC, 10%.

[0235] Soluble H-151 exhibited an inhibitory effect on LNP-DNA-induced IRF activation (as indicated by cytokine induction), and this effect was more pronounced when H-151 was encapsulated in DNA-LNPs (Figure 1). Example 2: In Vivo LNP-encapsulated H-151 inhibits DNA-LNP-induced cytokine release

[0236] BALB / c mice were injected with 10 μg of DNA-LNP or 10 μg of DNA-LNP encapsulated with H-151. H-151 was administered at a dose of about 1-2 μg / mouse (about 0.04-0.08 mg / kg mouse). Cytokine levels in plasma were measured 4 hours after injection. Figures 2A, 2B, 2C and 2D show the ability of DNA-LNP encapsulated H-151 to inhibit DNA-induced IFN-β (Figure 2A), IFN-α (Figure 2B), IFN-γ (Figure 2C) and IL-6 (Figure 2D). DNA-LNP was as described in Example 1 above. Example 3: In Vivo Inhibitory Effect of RO3150 and GSK690693 on DNA-LNP-Induced Cytokine Release

[0237] BALB / c mice were pretreated with dexamethasone, GSK690693, or RO3150 before DNA-LNP administration, and plasma cytokine concentrations were measured 4 hours after DNA-LNP administration. DNA-LNPs were composed of (1) a DNA plasmid (a nanoplasmid expression cassette encoding hFIX); and (2) GenVoy-ILM TM Consisting of LNP. GenVoy-ILM TM LNPs contain 50% ionizable lipids, 10% DSPC, 37.5% cholesterol, and 2.5% stabilizer (PEG-Lipid) (see Roces et al., Pharmaceutics, 2020 12, 1095). Pretreatment consisted of 200 μg dexamethasone administered intraperitoneally approximately 1 hour prior to DNA-LNP administration, 312.5 μg GSK69063 administered intraperitoneally approximately 1 hour prior to DNA-LNP administration, or 60 μg RO3015 administered intravenously immediately prior to DNA-LNP administration.

[0238] Figures 3A, 3B, 3C, 3D, 3E, 3F, 3G, and 3H show the ability of RO3150, GSK690693, and dexamethasone to inhibit the cytokine / chemokine levels induced by DNA-LNP. At the doses employed, dexamethasone and RO3150 were broadly active, while GSK690693 reduced most cytokine / chemokine levels except for IL-6 and KC / GRO. Example 4: Blockade of STING signaling

[0239] Wild-type (WT) mice and mice carrying Goldentiquet (STING(Gt)), a missense mutation in STING, a cytoplasmic double-stranded DNA (dsDNA) sensor (n=5 per group), were administered DNA-LNPs (0.625mpk (25μg / mouse) and 1.25mpk (50μg / mouse), respectively) systemically (bolus injection via tail vein) at two time points (t=0 and t=41 days). DNA-LNPs consisted of nanoplasmid DNA encoding human coagulation factor IX (hFIX) encapsulated in LNPs containing 35% bCKK-E12 lipid (described further below in IA); 2.4% C14-PEG2000; 0.1% GalNAc PEG C18; 46.5% cholesterol; and 16% DOPE. Figures 4A, 4B, and 4C show plasma cytokine levels (IL-6, IFNα, and IFNγ, respectively) measured 4 hours after dosing on day 41 and compared to pooled pre-dose plasma levels ("baseline") in WT mice (i.e., measured in WT mice not administered DNA-LNP). Figure 4D tracks survival of mice from each group out to day 70. Figure 4E shows transgenic hFIX protein levels in plasma measured by ELISA at various time points after dosing in surviving mice from each group out to day 70. Blockade of STING signaling improves DNA-LNP tolerability, survival, and transgene expression.

[0240] Genetic blockade of STING (Goldenticket mice) resulted in decreased IL-6 (Figure 4A), decreased IFNα (Figure 4B), decreased IFN-γ (Figure 4C), and improved survival (Figure 4D) in mice administered DNA-LNP gene therapy compared to WT mice. STING blockade also increased expression of the DNA-LNP gene therapy transgene compared to WT mice (Figure 4E).

[0241] These data support targeting STING signaling as an approach to improve the tolerability and efficacy of DNA-LNP gene therapy, with the potential benefits of a dsDNA payload that may reduce the susceptibility of immune cells (and possibly target cells) to inflammatory responses.

[0242] Although the invention has been described and illustrated with reference to specific embodiments thereof, those skilled in the art will appreciate that various adaptations, changes, modifications, substitutions, deletions, or additions of procedures and protocols may be made without departing from the spirit and scope of the invention.

Claims

A cytoplasmic DNA sensing inhibitor for use in a method for intracellular delivery of DNA to a subject, comprising: The cytoplasmic DNA sensing inhibitor is selected from the group consisting of a cyclic GMP-AMP synthase-interferon gene stimulator (cGAS)-STING pathway inhibitor and an inflammasome pathway inhibitor; The intracellular delivery method is as follows: (a) The cytoplasmic DNA sensing inhibitor, and (b) A first nanoparticle containing the DNA A cytoplasmic DNA sensing inhibitor, which comprises the step of administering, and step (b) is carried out before, simultaneously with, or after step (a).

2. When the first nanoparticle is a lipid nanoparticle, the cytoplasmic DNA sensing inhibitor according to claim 1, which is at least one of the following: (i) The cytoplasmic DNA sensing inhibitor is at least an inflammasome pathway inhibitor; (ii) The lipid nanoparticle does not contain an endosome lysing agent; (iii) The DNA is circular; (iv) The DNA is not closed circular DNA; or (v) The cytoplasmic DNA sensing inhibitor is provided in a second nanoparticle, and the second nanoparticle can have the same or different composition as the first nanoparticle.

3. The DNA is a DNA vector containing a transgene operably linked to a regulatory element, preferably the transgene is operably linked to a promoter; more preferably, the DNA vector contains, from 5' to 3', the promoter, the transgene, and a polyadenylation signal and a termination signal. The cytoplasmic DNA sensing inhibitor according to claim 1.

4. The cytoplasmic DNA sensing inhibitor is a cGAS-STING pathway inhibitor, preferably the cGAS-STING pathway inhibitor is a cGAS inhibitor, or a STING inhibitor, or a TBK1 inhibitor, or the cGAS-STING pathway inhibitor is (a) selected from the group consisting of H-151, GSK-690693, RU-521, RO-3150, CYT387 and GSK8612, or a pharmaceutically acceptable salt thereof; or (b) a compound in Table 1, Table 2, or Table 3, or a pharmaceutically acceptable salt thereof. The cytoplasmic DNA sensing inhibitor according to claim 1.

5. The cytoplasmic DNA sensing inhibitor is an inflammasome pathway inhibitor, preferably the inflammasome pathway inhibitor is an AIM2 inhibitor, more preferably the inflammasome pathway inhibitor is a polynucleotide having the sequence of SEQ ID NO: 1 or SEQ ID NO: 2, the cytoplasmic DNA sensing inhibitor according to claim 1 or 2.

6. The transgene encodes a viral antigen, a bacterial antigen, a therapeutic protein, a short hairpin RNA (shRNA), a small interfering RNA (siRNA), a microRNA (miRNA), a ribozyme, an antisense RNA, a CRISPR (clustered regularly interspaced short palindromic repeats) / Cas9 construct, a zinc finger nuclease (ZFN), or a transcription activator-like effector nuclease (TALEN), the cytoplasmic DNA sensing inhibitor according to claim 3 or 4.

7. The DNA is circular DNA, the cytoplasmic DNA sensing inhibitor according to claim 1 or 2.

8. The cytoplasmic DNA sensing inhibitor is provided in a second nanoparticle, and the second nanoparticle has substantially the same composition as the first nanoparticle, the cytoplasmic DNA sensing inhibitor according to claim 1 or 2.

9. The DNA vector and the cytoplasmic DNA sensing inhibitor are provided together in the first nanoparticle, preferably the first nanoparticle is a lipid nanoparticle or a lipid polymer nanoparticle, more preferably the first nanoparticle is configured to release the cytoplasmic DNA sensing inhibitor before the release of the DNA or the DNA vector, the cytoplasmic DNA sensing inhibitor according to claim 3 or 4.

10. The first nanoparticle is a lipid nanoparticle or a lipid polymer nanoparticle, the cytoplasmic DNA sensing inhibitor according to claim 3 or 4.

11. The cytoplasmic DNA sensing inhibitor is administered from approximately the same time as the administration of the DNA or the DNA vector to about 4 hours before, the cytoplasmic DNA sensing inhibitor according to claim 3 or 4.

12. Both an inflammasome inhibitor and a cGAS-STING inhibitor are administered, the cytoplasmic DNA sensing inhibitor according to claim 1 or 2.

13. The cytoplasmic DNA sensing inhibitor according to claim 3 or 4, wherein the DNA substantially comprises double-stranded DNA and the DNA vector substantially comprises double-stranded DNA.

14. The cytoplasmic DNA sensing inhibitor according to claim 3 or 4, wherein the subject is a human patient and the method provides a therapeutically effective amount of the transgene.

15. a. DNA; and b. A nanoparticle composition comprising at least one cytoplasmic DNA sensing inhibitor selected from the group consisting of a cyclic GMP-AMP synthase (cGAS)-STING pathway inhibitor and an inflammasome pathway inhibitor, preferably wherein the DNA and the cytoplasmic DNA sensing inhibitor are the DNA and the cytoplasmic DNA sensing inhibitor according to claim 3 or 4.

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