US20150111955A1 - Aav vector compositions and methods for gene transfer to cells, organs and tissues - Google Patents

Aav vector compositions and methods for gene transfer to cells, organs and tissues Download PDF

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US20150111955A1
US20150111955A1 US14/378,886 US201314378886A US2015111955A1 US 20150111955 A1 US20150111955 A1 US 20150111955A1 US 201314378886 A US201314378886 A US 201314378886A US 2015111955 A1 US2015111955 A1 US 2015111955A1
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aav
protein
gene
factor
disease
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Katherine A. High
Federico Mingozzi
Junwei Sun
Philip Johnson
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Childrens Hospital of Philadelphia CHOP
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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
    • C12N15/86—Viral vectors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2750/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssDNA viruses
    • C12N2750/00011—Details
    • C12N2750/14011—Parvoviridae
    • C12N2750/14111—Dependovirus, e.g. adenoassociated viruses
    • C12N2750/14141—Use of virus, viral particle or viral elements as a vector
    • C12N2750/14143—Use of virus, viral particle or viral elements as a vector viral genome or elements thereof as genetic vector

Definitions

  • a loss of function genetic disorder is hemophilia, an inherited bleeding disorder caused by deficiency in either coagulation factor VIII (FVIII, hemophilia A) or factor IX (FIX, hemophilia B).
  • FVIII coagulation factor VIII
  • FIX factor IX
  • a gain of function genetic disorder is Huntington's disease, a disease caused by a pathologic “HTT” gene (encodes the huntingtin protein) that encodes a mutated protein that accumulates within and leads to gradual destruction of neurons, particularly in the basal ganglia and the cerebral cortex.
  • hemophilia is ideal for gene transfer based therapy as 1) the therapeutic window is very wide, as levels just above 1% of normal already can result in a change in phenotype from severe to moderate, and levels of 100% are not associated to any side effects; 2) tissue specific expression of the therapeutic transgene is not strictly required; and 3) there is a considerable experience in measuring the endpoints of therapeutic efficacy. Furthermore, liver expression of clotting factor has been demonstrated to induce immunological tolerance to the clotting factor itself, reducing the likelihood of potentially harmful immune responses against clotting factor.
  • adeno-associated virus (AAV) vectors are recognized as the gene transfer vectors of choice since they have the best safety and efficacy profile for the delivery of genes in vivo.
  • AAV2 and AAV8 have been used to target the liver of humans affected by severe hemophilia B. Both vectors worked efficiently and in the case of AAV8 long-term expression of the therapeutic transgene was documented. Recent data in humans showed that targeting the liver with an AAV vector achieves long-term expression of the FIX transgene at therapeutic levels.
  • the invention provides adeno-associated virus (AAV) serotype AAV-Rh74 vector, and related AAV vectors.
  • AAV adeno-associated virus
  • Such vectors include AAV-Rh74 which target hepatocyte cells of the liver, among other cell types.
  • AAV-Rh74 and related AAV vectors drive expression of the polynucleotide in cells.
  • Polynucleotides that encode proteins, such as proteins for therapeutic applications are able to be expressed at therapeutic levels after administration.
  • AAV-Rh74 and related AAV vector mediated polynucleotide transfer produced protein expression levels that were significantly higher than several other serotypes currently studied in preclinical and clinical settings (see, e.g., FIGS. 1 and 2 ).
  • AAV-Rh74 could target polynucleotides to the liver with efficiency at least comparable or superior to the gold standard for liver transduction, AAV8, both in mice and in hemophilia B dogs.
  • AAV-Rh74 can be used to deliver polynucleotides, such as gene coding sequences, to express proteins that provide a desirable or therapeutic benefit, as well as for inhibitory nucleotides that reduce or inhibit expression of an undesirable or defective gene, thereby treating a variety of diseases.
  • AAV-Rh74 can be used to deliver therapeutic genes (e.g., FIX, FVIII) to treat hemophilia A, B, and to deliver genes for a wide range of other metabolic or plasma protein deficiencies, or to deliver genes for other therapeutic purposes, such as but not limited to genes encoding zinc finger nucleases to carry out genome editing in the liver, and for local (liver) delivery of immunomodulatory agents such as alpha-interferon for treatment of hepatitis virus infections, or to treat virtually any disease that requires either liver transduction or presence of the therapeutic transgene product in the bloodstream (which can be achieved by targeting the transgenes for liver expression).
  • therapeutic genes e.g., FIX, FVIII
  • AAV-Rh74 and related vectors can be used in a greater percentage of humans which otherwise would not be eligible for gene transfer, for example, humans that may be sero-positive for other AAV serotypes (e.g., AAV1, AAV2, AAV3, AAV4, AAV5, AAV6, AAV7, AAV8, AAV9, AAV10, AAV11, etc.).
  • AAV-Rh74 can be efficiently produced at high titers (Table 2).
  • AAV-Rh74 and related vectors can be produced in large amounts for more prevalent clinical diseases.
  • a method includes administering an adeno-associated virus (AAV) vector that includes a heterologous polynucleotide sequence to a mammal or a cell of a mammal under suitable conditions to deliver or transfer the heterologous polynucleotide sequence into the mammal or the cell of a mammal, thereby delivering or transferring the heterologous polynucleotide.
  • AAV adeno-associated virus
  • the method allows transfer/delivery of the heterologous polynucleotide into the mammal and/or cell.
  • the method allows transfer/delivery of the heterologous polynucleotide into the mammal and/or cell, and subsequent transcription of the heterologous polynucleotide thereby forming a transcript.
  • the method allows transfer/delivery of the heterologous polynucleotide into the cell, subsequent transcription to form a transcript and subsequent translation to form a gene product (protein).
  • a heterologous polynucleotide sequence is operably linked to an expression control element conferring transcription of the heterologous polynucleotide sequence, and optionally subsequent translation of the transcript.
  • Vector dose 2.5 10 vector genomes per mouse.
  • FIX transgene product (FIX protein) plasma levels were measured by ELISA at weeks 1, 2, and 4 post gene transfer.
  • AAV-Rh74 conferred the highest levels of FIX transgene expression.
  • FIG. 2 shows canine FIX plasma levels in hemophilia B dogs after the delivery of 3 12 vector genomes per kilogram (kg) of weight.
  • AAV vectors were infused intravenously (IV) though the saphenous vein and FIX levels were monitored by ELISA. Expression of the therapeutic FIX transgene was driven by a liver specific promoter.
  • AAV8 and AAV-Rh74 vectors performed roughly equally in hemophilia B dogs and were both superior to AAV6.
  • FIG. 3 shows AAV-Rh74 VP1, VP2, and VP3 amino acid sequences and, for VP1, polynucleotide (DNA) sequence (SEQ ID NOs:1-4).
  • FIG. 4 shows administration of AAV8 and AAVrh74 vector expressing human Factor IX (FIX) (under the control of a liver-specific promoter) to rhesus macaques, a non-human primate, and expression of FIX in the animals.
  • Animals receiving the AAVrh74-FIX vectors (last two bars towards the right margin) expressed the FIX transgene at higher levels compared to the other groups of animals injected at the same dose.
  • the invention is based, at least in part, on data indicating that adeno-associated virus (AAV) serotype AAV-Rh74 has a high tropism for hepatocytes, which are cells of the liver.
  • AAV-Rh74 can drive therapeutic levels of expression in liver after intravenous administration.
  • AAV-Rh74 mediated gene transfer/delivery produced protein expression levels that were significantly higher than several other serotypes (see, e.g., FIGS. 1 and 2 ).
  • AAV-Rh74 targets genes for delivery to the liver with efficiency at least comparable or superior to the gold standard for liver transduction, AAV8, both in mice and in hemophilia B dogs.
  • AAV-Rh74 can be used to transfer/deliver polynucleotides, such as coding sequences (genes) for proteins that provide a desirable or therapeutic benefit, as well as inhibitory (e.g., anti-sense) nucleic acid that reduce or inhibit expression of an undesirable or defective (e.g., pathologic) gene, thereby treating a variety of diseases.
  • AAV-Rh74 can be used to transfer/deliver therapeutic genes to treat hemophilia A, B, and to transfer/deliver genes for a wide range of other metabolic or plasma protein deficiencies, or for other therapeutic purposes, such as but not limited to genes encoding zinc finger nucleases to carry out genome editing in the liver, and for local (liver) delivery of immunomodulatory agents such as alpha-interferon for treatment of hepatitis virus infections, and to treat virtually any disease that requires either liver transduction or presence of the therapeutic transgene product in the bloodstream (which can be achieved by targeting the transgenes for liver expression).
  • immunomodulatory agents such as alpha-interferon for treatment of hepatitis virus infections
  • adeno-associated virus (AAV) serotype AAV-Rh74 and related AAV vectors provide delivery of polynucleotide sequences to cells ex vivo, in vitro and in vivo.
  • Such polynucleotide sequences can encode proteins such that the cells into which the polynucleotides are delivered express the encoded proteins.
  • AAV-Rh74 and related AAV vectors can include polynucleotides encoding a desired protein or peptide, or a polynucleotide that when transcribed comprises an inhibitory sequence (e.g., RNA), for example, a sequence that targets a gene for inhibition of expression.
  • RNA inhibitory sequence
  • Vector delivery or administration to a subject therefore provides not only polynucleotides encoding proteins and peptides to the subject, but also inhibitory nucleic acids that target genes for inhibition of expression or function in the subject.
  • adeno-associated virus (AAV) serotype AAV-Rh74 and related AAV vectors, including polynucleotide sequences encoding peptides and proteins, as well as polynucleotide sequences which directly or when transcribed comprise inhibitory nucleic acids that target genes for inhibition of expression or function, are provided.
  • AAV adeno-associated virus
  • Such AAV-Rh74 and related AAV vector serotypes are distinct from other AAV serotypes, including, for example, AAV1-AAV11 or Rh10 (e.g., distinct from VP1, VP2, and/or VP3 sequences of any of AAV1-AAV11, or Rh10 serotypes).
  • serotype is a distinction used to refer to an AAV having a capsid that is serologically distinct from other AAV serotypes. Serologic distinctiveness is determined on the basis of the lack of cross-reactivity between antibodies to one AAV as compared to another AAV. Such cross-reactivity differences are usually due to differences in capsid protein sequences/antigenic determinants (e.g., due to VP1, VP2, and/or VP3 sequence differences of AAV serotypes).
  • AAV-Rh74 has gene/protein sequences identical to sequences characteristic for AAV-Rh74 (see, e.g., VP1, VP2, VP3 of FIG. 3 ).
  • an “AAV vector related to AAV-Rh74” and grammatical variations thereof refers to one or more AAV proteins (e.g., VP1, VP2, and/or VP3 sequences) that has substantial sequence identity to one or more polynucleotides or polypeptide sequences that comprise AAV-Rh74.
  • Such AAV vectors related to AAV-Rh74 can therefore have one or more distinct sequences from AAV-Rh74, but can exhibit substantial sequence identity to one or more genes and/or have one or more functional characteristics of AAV-Rh74 (e.g., such as cell/tissue tropism).
  • Exemplary AAV-Rh74 sequences include VP1, VP2, and/or VP3 set forth in FIG. 3 .
  • an AAV vector related to AAV-Rh74 has a polynucleotide, polypeptide or subsequence thereof that includes or consists of a sequence at least 80% or more (e.g., 85%, 90%, 95%, 96%, 97%, 98%, 99%, 99.5%, etc.) identical to one or more AAV-Rh74 VP1, VP2, and/or VP3 sequences set forth in FIG. 3 .
  • methods and uses include AAV-Rh74 sequences (polypeptides and nucleotides) and subsequences thereof that exhibit less than 100% sequence identity to a reference AAV-Rh74 gene or protein sequence (e.g., VP1, VP2, and/or VP3 sequences set forth in FIG. 3 ), but are distinct from and not identical to known AAV genes or proteins, such as AAV1-AAV11, AAV-Rh10, genes or proteins, etc.
  • an AAV-Rh74 polypeptide or subsequence thereof includes or consists of a sequence at least 80% or more identical, e.g., 85%, 85%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99.5%, etc., i.e. up to 100% identical to any reference AAV-Rh74 sequence or subsequence thereof (e.g., VP1, VP2 and/or VP3 sequences set forth in FIG. 3 ).
  • AAV vectors including AAV-Rh74, and AAV-Rh74 related vectors, can be constructed using recombinant techniques that are known to the skilled artisan, to include one or more heterologous polynucleotide sequences flanked with functional AAV ITRs. Incorporation of a heterologous polynucleotide defines the AAV as a recombinant vector, or an “rAAV vector.”
  • Such vectors can have one or more of the wild type AAV genes deleted in whole or in part, for example, a rep and/or cap gene, but retain at least one functional flanking ITR sequence, as necessary for the rescue, replication, and packaging of the AAV particle.
  • an AAV vector includes sequences required in cis for viral replication and packaging (e.g., functional ITRs).
  • polynucleotide and “nucleic acid” are used interchangeably herein to refer to all forms of nucleic acid, oligonucleotides, including deoxyribonucleic acid (DNA) and ribonucleic acid (RNA).
  • Polynucleotides include genomic DNA, cDNA and antisense DNA, and spliced or unspliced mRNA, rRNA tRNA and inhibitory DNA or RNA (RNAi, e.g., small or short hairpin (sh)RNA, microRNA, small or short interfering (si)RNA, trans-splicing RNA, or antisense RNA).
  • RNAi e.g., small or short hairpin (sh)RNA, microRNA, small or short interfering (si)RNA, trans-splicing RNA, or antisense RNA.
  • Polynucleotides include naturally occurring, synthetic, and intentionally altered or modified polynucleotides as well as analogues and derivatives. Polynucleotides can be single, double, or triplex, linear or circular, and can be of any length.
  • a “heterologous” polynucleotide merely refers to a polynucleotide inserted into AAV for purposes of AAV mediated transfer/delivery of the polynucleotide into a cell. Heterologous polynucleotides are typically distinct from AAV nucleic acid. Once transferred/delivered into the cell, a heterologous polynucleotide, contained within the rAAV virion, can be expressed (e.g., transcribed, and translated if appropriate). Alternatively, a transferred/delivered heterologous polynucleotide in a cell, contained within the rAAV virion, need not be expressed.
  • heterologous is not always used herein in reference to polynucleotides, reference to a polynucleotide even in the absence of the modifier “heterologous” includes heterologous polynucleotides in spite of the omission.
  • polypeptides include full-length native sequences, as with naturally occurring proteins, as well as functional subsequences, modified forms or sequence variants so long as the subsequence, modified form or variant retains some degree of functionality of the native full-length protein.
  • polypeptides, proteins and peptides encoded by the polynucleotide sequences can be but are not required to be identical to the endogenous protein that is defective, or whose expression is insufficient, or deficient in the treated mammal.
  • adeno-associated virus (AAV) serotype AAV-Rh74, and related AAV vectors can be used to introduce/deliver polynucleotides stably or transiently into cells and progeny thereof.
  • the term “transgene” is used to conveniently refer to such a heterologous polynucleotide that has been introduced into a cell or organism.
  • Transgenes include any polynucleotide, such as a gene that encodes a polypeptide or protein, a polynucleotide that is transcribed into an inhibitory polynucleotide, or a polynucleotide that is not transcribed (e.g., lacks a expression control element, such as a promoter that drives transcription).
  • transgene in a cell having a transgene, the transgene has been introduced/transferred by AAV “transformation” of the cell.
  • a cell or progeny thereof into which the transgene has been introduced is referred to as a “transformed cell” or “transformant.”
  • a transgene is included in progeny of the transformant or becomes a part of the organism that develops from the cell.
  • a “transformed” or “transfected” cell means a genetic change in a cell following incorporation of an exogenous molecule, for example, a polynucleotide or protein (e.g., a transgene) into the cell.
  • a “transfected” or “transformed” cell is a cell into which, or a progeny thereof in which an exogenous molecule has been introduced, for example.
  • the cell(s) can be propagated and the introduced protein expressed, or nucleic acid transcribed.
  • polynucleotides encoding gene products (proteins) which are useful in accordance with the invention include, but are not limited to: genes that comprise or encode CFTR (cystic fibrosis transmembrane regulator protein), a blood coagulation (clotting) factor (Factor XIII, Factor IX, Factor X, Factor VIII, Factor VIIa, protein C etc.) including gain of function blood coagulation factors, an antibody, retinal pigment epithelium-specific 65 kDa protein (RPE65), erythropoietin, LDL receptor, lipoprotein lipase, ornithine transcarbamylase, ⁇ -globin, ⁇ -globin, spectrin, ⁇ -antitrypsin, adenosine deaminase (ADA), a metal transporter (ATP7A or ATP7), sulfamidase, an enzyme involved in lysosomal storage disease (ARSA), hypoxant
  • CFTR
  • hCDR1 [Sharabi et al., Proc Natl Acad Sci USA. 2006 Jun. 6; 103(23):8810-5], insulin, glucokinase, guanylate cyclase 2D (LCA-GUCY2D), Rab escort protein 1 (Choroideremia), LCA 5 (LCA-Lebercilin), ornithine ketoacid aminotransferase (Gyrate Atrophy), Retinoschisin 1 (X-linked Retinoschisis), USH1C (Usher's Syndrome 1C), X-linked retinitis pigmentosa GTPase (XLRP), MERTK (AR forms of RP: retinitis pigmentosa), DFNB1 (Connexin 26 deafness), ACHM 2, 3 and 4 (Achromatopsia), PKD-1 or PKD-2 (Polycystic kidney disease), TPP1,
  • non-mammalian forms of polynucleotides encoding gene products including the non-limiting genes and proteins disclosed herein are expressly included, either known or unknown.
  • the invention includes genes and proteins from non-mammals, mammals other than humans, and humans, which genes and proteins function in a substantially similar manner to the human genes and proteins described herein.
  • a non-limiting example of non-mammalian gene is a Fok nuclease domain, which is bacterial in origin.
  • Non-limiting examples of mammalian non-human FIX sequences are described in Yoshitake et al., 1985, supra; Kurachi et al., 1995, supra; Jallat et al., 1990, supra; Kurachi et al., 1982, Proc. Natl. Acad. Sci. USA 79:6461-6464; Jaye et al., 1983, Nucl. Acids Res. 11:2325-2335; Anson et al., 1984, EMBO J.
  • Polynucleotides, polypeptides and subsequences thereof include modified and variant forms.
  • the terms “modify” or “variant” and grammatical variations thereof mean that a polynucleotide, polypeptide or subsequence thereof deviates from a reference sequence. Modified and variant sequences may therefore have substantially the same, greater or less activity or function than a reference sequence, but at least retain partial activity or function of the reference sequence.
  • the invention also includes naturally and non-naturally occurring variants.
  • variants include gain and loss of function variants.
  • wild type human FIX DNA sequences which protein variants or mutants retain activity, or are therapeutically effective, or are comparably or even more therapeutically active than invariant human FIX in the methods and uses of the invention.
  • collagen IV serves to trap FIX, meaning that when introduced into the muscle tissue of a mammal some of the FIX is not available for participation in blood coagulation because it is retained in the interstitial spaces in the muscle tissue.
  • a mutation in the sequence of FIX that results in a protein with reduced binding to collagen IV is a mutant useful in the methods of the invention, for example, for treatment of hemophilia.
  • An example of such a mutant human FIX gene encodes a human FIX protein with the amino acid alanine in place of lysine in the fifth amino acid position from the beginning of the mature protein.
  • Non-limiting examples of modifications include one or more amino acid substitutions (e.g., 1-3, 3-5, 5-10, 10-15, 15-20, 20-25, 25-30, 30-40, 40-50, or more residues), additions (e.g., insertions or 1-3, 3-5, 5-10, 10-15, 15-20, 20-25, 25-30, 30-40, 40-50, or more residues) and deletions (e.g., subsequences or fragments) of a reference sequence.
  • a modified or variant sequence retains at least part of a function or an activity of unmodified sequence.
  • Such modified forms and variants can have less than, the same, or greater, but at least a part of, a function or activity of a reference sequence, for example, as described herein.
  • a variant can have one or more non-conservative or a conservative amino acid sequence differences or modifications, or both.
  • a “conservative substitution” is the replacement of one amino acid by a biologically, chemically or structurally similar residue. Biologically similar means that the substitution does not destroy a biological activity. Structurally similar means that the amino acids have side chains with similar length, such as alanine, glycine and serine, or a similar size. Chemical similarity means that the residues have the same charge or are both hydrophilic or hydrophobic.
  • Particular examples include the substitution of one hydrophobic residue, such as isoleucine, valine, leucine or methionine for another, or the substitution of one polar residue for another, such as the substitution of arginine for lysine, glutamic for aspartic acids, or glutamine for asparagine, serine for threonine, and the like.
  • Particular examples of conservative substitutions include the substitution of a hydrophobic residue such as isoleucine, valine, leucine or methionine for another, the substitution of a polar residue for another, such as the substitution of arginine for lysine, glutamic for aspartic acids, or glutamine for asparagine, and the like.
  • conservative amino acid substitutions typically include substitutions within the following groups: glycine, alanine; valine, isoleucine, leucine; aspartic acid, glutamic acid; asparagine, glutamine; serine, threonine; lysine, arginine; and phenylalanine, tyrosine.
  • a “conservative substitution” also includes the use of a substituted amino acid in place of an unsubstituted parent amino acid.
  • the invention includes gene and protein variants (e.g., of polynucleotides encoding proteins described herein) which retain one or more biological activities (e.g., function in blood clotting, etc.).
  • variants of proteins or polypeptides include proteins or polypeptides which have been or may be modified using recombinant DNA technology such that the protein or polypeptide possesses altered or additional properties, for example, variants conferring enhanced protein stability in plasma or enhanced activity of the protein.
  • Variants can differ from a reference sequence, such as naturally occurring polynucleotides, proteins or peptides.
  • a naturally and non-naturally occurring variant gene will typically be at least about 50% identical, more typically about 70% identical, even more typically about 80% identical (90% or more identity) to the reference gene.
  • a naturally and non-naturally occurring variant protein will typically be at least about 70% identical, more typically about 80% identical, even more typically about 90% or more identity to the reference protein, although substantial regions of non-identity are permitted in non-conserved regions (e.g., less, than 70% identical, such as less than 60%, 50% or even 40%).
  • sequences have at least 60%, 70%, 75% or more identity (e.g., 80%, 85% 90%, 95%, 96%, 97%, 98%, 99% or more identity) to a reference sequence.
  • identity e.g., 80%, 85% 90%, 95%, 96%, 97%, 98%, 99% or more identity
  • identity means that two or more referenced entities are the same, when they are “aligned” sequences.
  • two polypeptide sequences are identical, they have the same amino acid sequence, at least within the referenced region or portion.
  • two polynucleotide sequences are identical, they have the same polynucleotide sequence, at least within the referenced region or portion.
  • the identity can be over a defined area (region or domain) of the sequence.
  • An “area” or “region” of identity refers to a portion of two or more referenced entities that are the same.
  • two protein or nucleic acid sequences are identical over one or more sequence areas or regions they share identity within that region.
  • An “aligned” sequence refers to multiple polynucleotide or protein (amino acid) sequences, often containing corrections for missing or additional bases or amino acids (gaps) as compared to a reference sequence
  • the identity can extend over the entire sequence length or a portion of the sequence.
  • the length of the sequence sharing the percent identity is 2, 3, 4, 5 or more contiguous polynucleotide or amino acids, e.g., 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, etc. contiguous amino acids.
  • the length of the sequence sharing identity is 20 or more contiguous polynucleotide or amino acids, e.g., 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, etc. contiguous amino acids.
  • the length of the sequence sharing identity is 35 or more contiguous polynucleotide or amino acids, e.g., 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 45, 47, 48, 49, 50, etc., contiguous amino acids.
  • the length of the sequence sharing identity is 50 or more contiguous polynucleotide or amino acids, e.g., 50-55, 55-60, 60-65, 65-70, 70-75, 75-80, 80-85, 85-90, 90-95, 95-100, 100-110, etc. contiguous polynucleotide or amino acids.
  • homology means that two or more referenced entities share at least partial identity over a given region or portion.
  • Areas, regions or domains of homology or identity mean that a portion of two or more referenced entities share homology or are the same. Thus, where two sequences are identical over one or more sequence regions they share identity in these regions.
  • Substantial homology means that a molecule is structurally or functionally conserved such that it has or is predicted to have at least partial structure or function of one or more of the structures or functions (e.g., a biological function or activity) of the reference molecule, or relevant/corresponding region or portion of the reference molecule to which it shares homology.
  • the extent of identity (homology) between two sequences can be ascertained using a computer program and mathematical algorithm.
  • Such algorithms that calculate percent sequence identity (homology) generally account for sequence gaps and mismatches over the comparison region or area.
  • a BLAST e.g., BLAST 2.0
  • search algorithm has exemplary search parameters as follows: Mismatch ⁇ 2; gap open 5; gap extension 2.
  • a BLASTP algorithm is typically used in combination with a scoring matrix, such as PAM100, PAM 250, BLOSUM 62 or BLOSUM 50.
  • FASTA e.g., FASTA2 and FASTA3
  • SSEARCH sequence comparison programs are also used to quantitate extent of identity (Pearson et al., Proc. Natl. Acad. Sci. USA 85:2444 (1988); Pearson, Methods Mol Biol. 132:185 (2000); and Smith et al., J. Mol. Biol. 147:195 (1981)).
  • Programs for quantitating protein structural similarity using Delaunay-based topological mapping have also been developed (Bostick et al., Biochem Biophys Res Commun. 304:320 (2003)).
  • Polynucleotides include additions and insertions, for example, heterologous domains.
  • An addition e.g., heterologous domain
  • additions and insertions e.g., a heterologous domain
  • Additions and insertions include chimeric and fusion sequences, which is a polynucleotide or protein sequence having one or more molecules not normally present in a reference native (wild type) sequence covalently attached to the sequence.
  • fusion or “chimeric” and grammatical variations thereof, when used in reference to a molecule means that a portions or part of the molecule contains a different entity distinct (heterologous) from the molecule as they do not typically exist together in nature. That is, for example, one portion of the fusion or chimera, includes or consists of a portion that does not exist together in nature, and is structurally distinct.
  • polynucleotide sequences include inhibitory and antisense nucleic acid sequences Inhibitory, antisense, miRNA, shRNA, and RNAi nucleic acids can modulate expression of a target gene.
  • Antisense includes single, double or triple stranded polynucleotides and peptide nucleic acids (PNAs) that bind RNA transcript or DNA (e.g., genomic DNA).
  • PNAs peptide nucleic acids
  • Oligonucleotides derived from the transcription initiation site of a target gene e.g., between positions ⁇ 10 and +10 from the start site, are another particular example.
  • Triplex forming antisense can bind to double strand DNA thereby inhibiting transcription of the gene.
  • RNAi is the use of single or double stranded RNA sequences for inhibiting gene expression (see, e.g., Kennerdell et al., Cell 95:1017 (1998); and Fire et al., Nature, 391:806 (1998)). Double stranded RNA sequences from a target gene coding region may therefore be used to inhibit or prevent gene expression/transcription in accordance with the methods and uses of the invention.
  • Antisense and RNAi can be produced based upon nucleic acids encoding target gene sequences (e.g., HTT), such as nucleic acid encoding mammalian and human HTT.
  • a single or double stranded nucleic acid e.g., RNA
  • can target HTT transcript e.g., mRNA).
  • genes e.g., genomic DNA
  • transcript of a pathogenic gene e.g, RNA or mRNA
  • pathogenic genes associated with polynucleotide repeat diseases such as huntingtin (HTT) gene, a gene associated with dentatorubropallidolusyan atropy (e.g., atrophin 1, ATN1); androgen receptor on the X chromosome in spinobulbar muscular atrophy, human Ataxin-1, -2, -3, and -7
  • Ca v 2.1 P/Q voltage-dependent calcium channel is encoded by the (CACNA1A), TATA-binding protein, Ataxin 8 opposite strand, also known as ATXN8OS, Serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform in spinocerebellar ataxia (type 1, 2, 3, 6, 7, 8,
  • the term “recombinant,” as a modifier of AAV, such as recombinant AAV-Rh74 and related AAV vectors, as well as a modifier of sequences such as recombinant polynucleotides and polypeptides, means that the compositions have been manipulated (i.e., engineered) in a fashion that generally does not occur in nature.
  • a particular example of a recombinant AAV would be where a polynucleotide that is not normally present in the wild-type AAV is within the AAV particle and/or genome.
  • a particular example of a recombinant polynucleotide would be where a polynucleotide (e.g., gene) encoding a protein is cloned into a vector, with or without 5′, 3′ and/or intron regions that the gene is normally associated within the AAV genome.
  • a polynucleotide e.g., gene
  • AAV AAV-Rh74 and related AAV vectors
  • sequences such as polynucleotides and polypeptides
  • recombinant forms of AAV, AAV-Rh74 and related AAV vectors, and sequences including polynucleotides and polypeptides are expressly included in spite of any such omission.
  • Polynucleotide sequences in accordance with the invention can be inserted into a vector.
  • vector refers to a plasmid, virus (e.g., AAV) or other vehicle that can be manipulated by insertion or incorporation of a polynucleotide.
  • vectors can be used for genetic manipulation (i.e., “cloning vectors”), to introduce/transfer polynucleotides into cells, and to transcribe or translate the inserted polynucleotide in cells.
  • a vector generally contains at least an origin of replication for propagation in a cell and expression control element (e.g., a promoter).
  • Control elements including expression control elements as set forth herein, present within a vector are included to facilitate proper transcription and if appropriate translation (e.g., splicing signal for introns, maintenance of the correct reading frame of the gene to permit in-frame translation of mRNA and, stop codons etc.).
  • appropriate translation e.g., splicing signal for introns, maintenance of the correct reading frame of the gene to permit in-frame translation of mRNA and, stop codons etc.
  • Vectors including AAV-Rh74 and related AAV vectors of the invention can include one or more “expression control elements.”
  • expression control elements are nucleic acid sequence(s), such as promoters and enhancers, that influence expression of an operably linked polynucleotide. Such elements typically act in cis but may also act in trans.
  • Expression control can be effected at the level of transcription, translation, splicing, message stability, etc.
  • an expression control element that modulates transcription is juxtaposed near the 5′ end of the transcribed polynucleotide (i.e., “upstream”).
  • Expression control elements can also be located at the 3′ end of the transcribed sequence (i.e., “downstream”) or within the transcript (e.g., in an intron).
  • Expression control elements can be located at a distance away from the transcribed sequence (e.g., 100 to 500, 500 to 1000, 2000 to 5000, 5000 to 10,000 or more nucleotides from the polynucleotide), even at considerable distances. Nevertheless, owing to the polynucleotide length limitations, for AAV-Rh74 and related AAV vectors, such expression control elements will typically be within 1 to 1000 nucleotides from the polynucleotide.
  • expression of the operably linked polynucleotide is at least in part controllable by the element (e.g., promoter) such that the element modulates transcription of the polynucleotide and, as appropriate, translation of the transcript.
  • the element e.g., promoter
  • a specific example of an expression control element is a promoter, which is usually located 5′ of the transcribed sequence.
  • Another example of an expression control element is an enhancer, which can be located 5′, 3′ of the transcribed sequence, or within the transcribed sequence.
  • Expression control elements and promoters include those active in a particular tissue or cell type, referred to herein as a “tissue-specific expression control elements/promoters.” Tissue-specific expression control elements are typically active in specific cell or tissue (e.g., liver, brain, central nervous system, spinal cord, eye, retina or lung). Expression control elements are typically active in these cells, tissues or organs because they are recognized by transcriptional activator proteins, or other regulators of transcription, that are unique to a specific cell, tissue or organ type.
  • Expression control elements also include ubiquitous or promiscuous promoters/enhancers which are capable of driving expression of a polynucleotide in many different cell types.
  • Such elements include, but are not limited to the cytomegalovirus (CMV) immediate early promoter/enhancer sequences, the Rous sarcoma virus (RSV) promoter/enhancer sequences and the other viral promoters/enhancers active in a variety of mammalian cell types, or synthetic elements that are not present in nature.
  • CMV cytomegalovirus
  • RSV Rous sarcoma virus
  • Expression control elements also can confer expression in a manner that is regulatable, that is, a signal or stimuli increases or decreases expression of the operably linked polynucleotide.
  • a regulatable element that increases expression of the operably linked polynucleotide in response to a signal or stimuli is also referred to as an “inducible element” (i.e., is induced by a signal).
  • an inducible element i.e., is induced by a signal.
  • Particular examples include, but are not limited to, a hormone (e.g., steroid) inducible promoter.
  • a regulatable element that decreases expression of the operably linked polynucleotide in response to a signal or stimuli is referred to as a “repressible element” (i.e., the signal decreases expression such that when the signal, is removed or absent, expression is increased).
  • the amount of increase or decrease conferred by such elements is proportional to the amount of signal or stimuli present; the greater the amount of signal or stimuli, the greater the increase or decrease in expression.
  • operable linkage or “operably linked” refers to a physical or functional juxtaposition of the components so described as to permit them to function in their intended manner.
  • the relationship is such that the control element modulates expression of the nucleic acid.
  • two DNA sequences operably linked means that the two DNAs are arranged (cis or trans) in such a relationship that at least one of the DNA sequences is able to exert a physiological effect upon the other sequence.
  • Vectors including AAV-Rh74 and related AAV vectors of the invention can include still additional nucleic acid elements.
  • These elements include, without limitation one or more copies of an AAV ITR sequence, a promoter/enhancer element, a transcription termination signal, 5′ or 3′ untranslated regions (e.g., polyadenylation sequences) which flank a polynucleotide sequence, or all or a portion of intron I.
  • Such elements also optionally include a transcription termination signal.
  • a particular non-limiting example of a transcription termination signal is the SV40 transcription termination signal.
  • intron element may enhance expression compared with expression in the absence of the intron element (Kurachi et al., 1995, supra).
  • AAV vectors typically accept inserts of DNA having a defined size range which is generally about 4 kb to about 5.2 kb, or slightly more. Thus, for shorter sequences, it may be necessary to include additional nucleic acid in the insert fragment in order to achieve the required length which is acceptable for the AAV vector.
  • Introns and intron fragments (e.g. portion of intron I of FIX) fulfill this requirement while also enhancing expression.
  • the invention is not limited to the inclusion of intron I sequences in the AAV vector, and include other introns or other DNA sequences in place of portions of intron I.
  • nucleic acid may be used in place of those recited for human FIX, particularly when polynucleotides encoding proteins other than human FIX are used in the AAV-Rh74 and related AAV vectors of the invention.
  • portion of intron I is meant region of intron I having a nucleotide length of from about 0.1 kb to about 1.7 kb, which region enhances expression of FIX, typically by about 1.5-fold or more on a plasmid or viral vector template when compared with expression of FIX in the absence of a portion of intron I.
  • a more specific portion is a 1.3 kb portion of intron 1.
  • Polynucleotides and polypeptides including modified forms can be made using various standard cloning, recombinant DNA technology, via cell expression or in vitro translation and chemical synthesis techniques. Purity of polynucleotides can be determined through sequencing, gel electrophoresis and the like. For example, nucleic acids can be isolated using hybridization or computer-based database screening techniques.
  • Such techniques include, but are not limited to: (1) hybridization of genomic DNA or cDNA libraries with probes to detect homologous nucleotide sequences; (2) antibody screening to detect polypeptides having shared structural features, for example, using an expression library; (3) polymerase chain reaction (PCR) on genomic DNA or cDNA using primers capable of annealing to a nucleic acid sequence of interest; (4) computer searches of sequence databases for related sequences; and (5) differential screening of a subtracted nucleic acid library.
  • PCR polymerase chain reaction
  • Polynucleotides and polypeptides including modified forms can also be produced by chemical synthesis using methods known in the art, for example, an automated synthesis apparatus (see, e.g., Applied Biosystems, Foster City, Calif.).
  • Peptides can be synthesized, whole or in part, using chemical methods (see, e.g., Caruthers (1980). Nucleic Acids Res. Symp. Ser. 215; Horn (1980); and Banga, A. K., Therapeutic Peptides and Proteins, Formulation, Processing and Delivery Systems (1995) Technomic Publishing Co., Lancaster, Pa.).
  • Peptide synthesis can be performed using various solid phase techniques (see, e.g., Roberge Science 269:202 (1995); Merrifield, Methods Enzymol. 289:3 (1997)) and automated synthesis may be achieved, e.g., using the ABI 431A Peptide Synthesizer (Perkin Elmer) in accordance with the manufacturer's instructions.
  • isolated when used as a modifier of a composition, means that the compositions are made by the hand of man or are separated, completely or at least in part, from their naturally occurring in vivo environment. Generally, isolated compositions are substantially free of one or more materials with which they normally associate with in nature, for example, one or more protein, nucleic acid, lipid, carbohydrate, cell membrane.
  • isolated does not exclude alternative physical forms of the composition, such as fusions/chimeras, multimers/oligomers, modifications (e.g., phosphorylation, glycosylation, lipidation) or derivatized forms, or forms expressed in host cells produced by the hand of man.
  • treatment methods and uses are provided that include therapeutic methods and uses.
  • Methods and uses of the invention are broadly applicable to diseases amenable to treatment by introducing a gene encoding a protein, or increasing or stimulating gene expression or function, e.g., gene addition or replacement.
  • Methods and uses of the invention are also broadly applicable to diseases amenable to treatment by reducing or decreasing gene expression or function, e.g., gene knockout or reduction of gene expression.
  • Non-limiting particular examples of diseases treatable in accordance with the invention include those set forth herein as well as a lung disease (e.g., cystic fibrosis), a blood coagulation or bleeding disorder (e.g., hemophilia A or hemophilia B with or without inhibitors), thalassemia, a blood disorder (e.g., anemia), Alzheimer's disease, Parkinson's disease, Huntington's disease, amyotrophic lateral sclerosis (ALS), epilepsy, lysosomal storage diseases, a copper or iron accumulation disorders (e.g., Wilson's or Menkes disease) lysosomal acid lipase deficiency, a neurological or neurodegenerative disorder, cancer, type 1 or type 2 diabetes, Gaucher's disease, Hurler's disease, adenosine deaminase deficiency, a metabolic defect (e.g., glycogen storage diseases), a retinal degenerative disease (such as RPE65 deficiency, choroid
  • a method of the invention includes: (a) providing adeno-associated virus (AAV) vector, said vector comprising a heterologous polynucleotide encoding a protein, wherein the heterologous polynucleotide sequence is operably linked to an expression control element conferring transcription of said polynucleotide sequence; and (b) administering an amount of the AAV vector to the mammal wherein said protein is expressed in the mammal.
  • AAV adeno-associated virus
  • expression of the protein provides a therapeutic benefit to the mammal
  • Methods of the invention include treatment methods, which result in any therapeutic or beneficial effect.
  • an methods of the invention further include inhibiting, decreasing or reducing one or more adverse (e.g., physical) symptoms, disorders, illnesses, diseases or complications caused by or associated with the disease, such as reduced blood clotting time, reduced administration dosage of supplemental clotting factor protein.
  • adverse e.g., physical symptoms, disorders, illnesses, diseases or complications caused by or associated with the disease, such as reduced blood clotting time, reduced administration dosage of supplemental clotting factor protein.
  • a therapeutic or beneficial effect of treatment is therefore any objective or subjective measurable or detectable improvement or benefit provided to a particular subject.
  • a therapeutic or beneficial effect can but need not be complete ablation of all or any particular adverse symptom, disorder, illness, or complication of a disease.
  • a satisfactory clinical endpoint is achieved when there is an incremental improvement or a partial reduction in an adverse symptom, disorder, illness, or complication caused by or associated with a disease, or an inhibition, decrease, reduction, suppression, prevention, limit or control of worsening or progression of one or more adverse symptoms, disorders, illnesses, or complications caused by or associated with the disease, over a short or long duration (hours, days, weeks, months, etc.).
  • compositions, methods and uses of the invention can be administered in a sufficient or effective amount to a subject in need thereof.
  • An “effective amount” or “sufficient amount” refers to an amount that provides, in single or multiple doses, alone or in combination, with one or more other compositions (therapeutic agents such as a drug), treatments, protocols, or therapeutic regimens agents, a detectable response of any duration of time (long or short term), an expected or desired outcome in or a benefit to a subject of any measurable or detectable degree or for any duration of time (e.g., for minutes, hours, days, months, years, or cured).
  • the AAV vector dose to achieve a therapeutic effect e.g., the dose in vector genomes/per kilogram of body weight (vg/kg) will vary based on several factors including, but not limited to: route of administration, the level of heterologous polynucleotide expression required to achieve a therapeutic effect, the specific disease treated, any host immune response to the AAV vector, a host immune response to the heterologous polynucleotide or expression product (protein), and the stability of the protein expressed.
  • route of administration e.g., the level of heterologous polynucleotide expression required to achieve a therapeutic effect
  • the specific disease treated any host immune response to the AAV vector
  • a host immune response to the heterologous polynucleotide or expression product (protein) protein
  • stability of the protein expressed e.g., the stability of the protein expressed.
  • One skilled in the art can readily determine a AAV virion dose range to treat a patient having a particular disease or disorder based on the aforementioned factors, as
  • doses will range from at least 1 ⁇ 10 8 , or more, for example, 1 ⁇ 10 9 , 1 ⁇ 10 10 , 1 ⁇ 10 11 , 1 ⁇ 10 12 , 1 ⁇ 10 13 or 1 ⁇ 10 14 , or more, vector genomes per kilogram (vg/kg) of the weight of the subject, to achieve a therapeutic effect.
  • hemophilia As an example, generally speaking, it is believed that, in order to achieve a therapeutic effect, a blood coagulation factor concentration that is greater than 1% of factor concentration found in a normal individual is needed to change a severe disease phenotype to a moderate one.
  • a severe phenotype is characterized by joint damage and life-threatening bleeds.
  • a blood coagulation factor concentration greater than 5% of normal is needed.
  • a typical dose is at least 1 ⁇ 10 10 vector genomes (vg) per kilogram (vg/kg) of the weight of the subject, or between about 1 ⁇ 10 10 to 1 ⁇ 10 11 vg/kg of the weight of the subject, or between about 1 ⁇ 10 11 to 1 ⁇ 10 12 vg/kg of the weight of the subject, or between about 1 ⁇ 10 12 to 1 ⁇ 10 13 vg/kg of the weight of the subject, to achieve a desired therapeutic effect.
  • an “effective amount” or “sufficient amount” for treatment typically are effective to provide a response to one, multiple or all adverse symptoms, consequences or complications of the disease, one or more adverse symptoms, disorders, illnesses, pathologies, or complications, for example, caused by or associated with the disease, to a measurable extent, although decreasing, reducing, inhibiting, suppressing, limiting or controlling progression or worsening of the disease is a satisfactory outcome.
  • An effective amount or a sufficient amount can but need not be provided in a single administration, may require multiple administrations, and, can but need not be, administered alone or in combination with another composition (e.g., agent), treatment, protocol or therapeutic regimen.
  • another composition e.g., agent
  • the amount may be proportionally increased as indicated by the need of the subject, type, status and severity of the disease treated or side effects (if any) of treatment.
  • an effective amount or a sufficient amount need not be effective or sufficient if given in single or multiple doses without a second composition (e.g., another drug or agent), treatment, protocol or therapeutic regimen, since additional doses, amounts or duration above and beyond such doses, or additional compositions (e.g., drugs or agents), treatments, protocols or therapeutic regimens may be included in order to be considered effective or sufficient in a given subject.
  • Amounts considered effective also include amounts that result in a reduction of the use of another treatment, therapeutic regimen or protocol, such as administration of recombinant clotting factor protein for treatment of a clotting disorder (e.g., hemophilia A or B).
  • An effective amount or a sufficient amount need not be effective in each and every subject treated, or a majority of treated subjects in a given group or population.
  • An effective amount or a sufficient amount means effectiveness or sufficiency in a particular subject, not a group or the general population. As is typical for such methods, some subjects will exhibit a greater response, or less or no response to a given treatment method or use. Thus, appropriate amounts will depend upon the condition treated, the therapeutic effect desired, as well as the individual subject (e.g., the bioavailability within the subject, gender, age, etc.).
  • a detectable or measurable improvement includes a subjective or objective decrease, reduction, inhibition, suppression, limit or control in the occurrence, frequency, severity, progression, or duration of the disease, or complication caused by or associated with the disease, or an improvement in a symptom or an underlying cause or a consequence of the disease, or a reversal of the disease.
  • a successful treatment outcome can lead to a “therapeutic effect,” or “benefit” of decreasing, reducing, inhibiting, suppressing, limiting, controlling or preventing the occurrence, frequency, severity, progression, or duration of a disease, or one or more adverse symptoms or underlying causes or consequences of the disease in a subject.
  • Treatment methods and uses affecting one or more underlying causes of the disease or adverse symptoms are therefore considered to be beneficial.
  • a decrease or reduction in worsening, such as stabilizing the disease, or an adverse symptom thereof, is also a successful treatment outcome.
  • a therapeutic benefit or improvement therefore need not be complete ablation of the disease, or any one, most or all adverse symptoms, complications, consequences or underlying causes associated with the disease.
  • a satisfactory endpoint is achieved when there is an incremental improvement in a subject's disease, or a partial decrease, reduction, inhibition, suppression, limit, control or prevention in the occurrence, frequency, severity, progression, or duration, or inhibition or reversal, of the disease (e.g., stabilizing one or more symptoms or complications), over a short or long duration of time (hours, days, weeks, months, etc.).
  • Effectiveness of a method or use such as a treatment that provides a potential therapeutic benefit or improvement of a disease, can be ascertained by various methods.
  • inventions and uses can be combined with any compound, agent, drug, treatment or other therapeutic regimen or protocol having a desired therapeutic, beneficial, additive, synergistic or complementary activity or effect.
  • exemplary combination compositions and treatments include second actives, such as, biologics (proteins), agents and drugs.
  • biologics (proteins), agents, drugs, treatments and therapies can be administered or performed prior to, substantially contemporaneously with or following any other method or use of the invention, for example, a therapeutic method of treating a subject for a blood clotting disease.
  • the compound, agent, drug, treatment or other therapeutic regimen or protocol can be administered as a combination composition, or administered separately, such as concurrently or in series or sequentially (prior to or following) an AAV vector of the invention.
  • the invention therefore provides combinations in which a method or use of the invention is in a combination with any compound, agent, drug, therapeutic regimen, treatment protocol, process, remedy or composition, set forth herein or known to one of skill in the art.
  • the compound, agent, drug, therapeutic regimen, treatment protocol, process, remedy or composition can be administered or performed prior to, substantially contemporaneously with or following administration of an AAV vector of the invention, to a subject.
  • Specific non-limiting examples of combination embodiments therefore include the foregoing or other compound, agent, drug, therapeutic regimen, treatment protocol, process, remedy or composition.
  • Methods and uses of the invention also include, among other things, methods and uses that result in a reduced need or use of another compound, agent, drug, therapeutic regimen, treatment protocol, process, or remedy.
  • a method or use of the invention has a therapeutic benefit if in a given subject a less frequent or reduced dose or elimination of administration of a recombinant clotting factor protein to supplement for the deficient or defective (abnormal or mutant) endogenous clotting factor in the subject.
  • methods and uses of reducing need or use of another treatment or therapy are provided.
  • subject refers to an animal, typically a mammal, such as humans, non-human primates (apes, gibbons, gorillas, chimpanzees, orangutans, macaques), a domestic animal (dogs and cats), a farm animal (poultry such as chickens and ducks, horses, cows, goats, sheep, pigs), and experimental animals (mouse, rat, rabbit, guinea pig).
  • Subjects include animal disease models, for example, mouse and other animal models of blood clotting diseases and others known to those of skill in the art.
  • Subjects appropriate for treatment in accordance with the invention include those having or at risk of producing an insufficient amount or having a deficiency in a functional gene product (protein), or produce an aberrant, partially functional or non-functional gene product (protein), which can lead to disease.
  • Subjects appropriate for treatment in accordance with the invention also include those having or at risk of producing an aberrant, or defective (mutant) gene product (protein) that leads to a disease such that reducing amounts, expression or function of the aberrant, or defective (mutant) gene product (protein) would lead to treatment of the disease, or reduce one or more symptoms or ameliorate the disease.
  • Target subjects therefore include subjects that have such defects regardless of the disease type, timing or degree of onset, progression, severity, frequency, or type or duration of the symptoms.
  • Subjects appropriate for treatment in accordance with the invention also include those having or at risk of producing antibodies against AAV.
  • AAV vectors can be administered or delivered to such subjects using several techniques. For example, empty capsid AAV (i.e., AAV lacking a heterologous polynucleotide) can be delivered to bind to the AAV antibodies thereby allowing the AAV vector bearing the heterologous polynucleotide to transform cells of the subject. Amounts of empty capsid AAV to administer can be calibrated based upon the amount of AAV antibodies produced in a particular subject.
  • AAV vector can be delivered by direct intramuscular injection (e.g., one or more slow-twitch fibers of a muscle).
  • a catheter introduced into the femoral artery can be used to delivery AAV vectors to liver via the hepatic artery.
  • Non-surgical means can also be employed, such as endoscopic retrograde cholangiopancreatography (ERCP), to deliver AAV vectors directly to the liver, thereby bypassing the bloodstream and AAV antibodies.
  • ERCP endoscopic retrograde cholangiopancreatography
  • Other ductal systems such as the ducts of the submandibular gland, can also be used as portals for delivering AAV vectors into a subject with preexisting anti-AAV antibodies.
  • “Prophylaxis” and grammatical variations thereof mean a method in which contact, administration or in vivo delivery to a subject is prior to disease. Administration or in vivo delivery to a subject can be performed prior to development of an adverse symptom, condition, complication, etc. caused by or associated with the disease.
  • a screen e.g., genetic
  • the subject may not manifest the disease.
  • Such subjects therefore include those screened positive for an insufficient amount or a deficiency in a functional gene product (protein), or produce an aberrant, partially functional or non-functional gene product (protein), which can lead to disease; and subjects that screen positive for an aberrant, or defective (mutant) gene product (protein) that leads to disease, even though such subjects do not manifest symptoms of the disease.
  • Methods and uses of the invention include delivery and administration systemically, regionally or locally, or by any route, for example, by injection, infusion, orally (e.g., ingestion or inhalation), or topically (e.g., transdermally).
  • Such delivery and administration include intravenously, intramuscularly, intraperitoneally, intradermally, subcutaneously, intracavity, intracranially, transdermally (topical), parenterally, e.g. transmucosally or rectally.
  • Exemplary administration and delivery routes include intravenous (i.v.), intraperitoneal (i.p.), intrarterial, intramuscular, parenteral, subcutaneous, intra-pleural, topical, dermal, intradermal, transdermal, parenterally, e.g. transmucosal, intra-cranial, intra-spinal, oral (alimentary), mucosal, respiration, intranasal, intubation, intrapulmonary, intrapulmonary instillation, buccal, sublingual, intravascular, intrathecal, intracavity, iontophoretic, intraocular, ophthalmic, optical, intraglandular, intraorgan, intralymphatic.
  • Doses for delivery and administration can be based upon current existing protocols, empirically determined, using animal disease models or optionally in human clinical trials. Initial study doses can be based upon animal studies set forth herein, for a mouse or dog, for example.
  • Doses can vary and depend upon whether the treatment is prophylactic or therapeutic, the type, onset, progression, severity, frequency, duration, or probability of the disease to which treatment is directed, the clinical endpoint desired, previous or simultaneous treatments, the general health, age, gender, race or immunological competency of the subject and other factors that will be appreciated by the skilled artisan.
  • the dose amount, number, frequency or duration may be proportionally increased or reduced, as indicated by any adverse side effects, complications or other risk factors of the treatment or therapy and the status of the subject. The skilled artisan will appreciate the factors that may influence the dosage and timing required to provide an amount sufficient for providing a therapeutic or prophylactic benefit.
  • Methods and uses of the invention as disclosed herein can be practiced within 1-2, 2-4, 4-12, 12-24 or 24-72 hours after a subject has been identified as having the disease targeted for treatment, has one or more symptoms of the disease, or has been screened and is identified as positive as set forth herein even though the subject does not have one or more symptoms of the disease.
  • methods and uses of the invention can be practiced 1-7, 7-14, 14-21, 21-48 or more days, months or years after a subject has been identified as having the disease targeted for treatment, has one or more symptoms of the disease, or has been screened and is identified as positive as set forth herein.
  • AAV vectors and other compositions, agents, drugs, biologics (proteins) can be incorporated into pharmaceutical compositions, e.g., a pharmaceutically acceptable carrier or excipient.
  • pharmaceutical compositions are useful for, among other things, administration and delivery to a subject in vivo or ex vivo.
  • the term “pharmaceutically acceptable” and “physiologically acceptable” mean a biologically acceptable formulation, gaseous, liquid or solid, or mixture thereof, which is suitable for one or more routes of administration, in vivo delivery or contact.
  • Such formulations include solvents (aqueous or non-aqueous), solutions (aqueous or non-aqueous), emulsions (e.g., oil-in-water or water-in-oil), suspensions, syrups, elixirs, dispersion and suspension media, coatings, isotonic and absorption promoting or delaying agents, compatible with pharmaceutical administration or in vivo contact or delivery.
  • Aqueous and non-aqueous solvents, solutions and suspensions may include suspending agents and thickening agents.
  • Such pharmaceutically acceptable carriers include tablets (coated or uncoated), capsules (hard or soft), microbeads, powder, granules and crystals.
  • Supplementary active compounds e.g., preservatives, antibacterial, antiviral and antifungal agents
  • compositions can be formulated to be compatible with a particular route of administration or delivery, as set forth herein or known to one of skill in the art.
  • pharmaceutical compositions include carriers, diluents, or excipients suitable for administration by various routes.
  • Formulations suitable for parenteral administration comprise aqueous and non-aqueous solutions, suspensions or emulsions of the active compound, which preparations are typically sterile and can be isotonic with the blood of the intended recipient.
  • Non-limiting illustrative examples include water, saline, dextrose, fructose, ethanol, animal, vegetable or synthetic oils.
  • penetrants can be included in the pharmaceutical composition.
  • Penetrants are known in the art, and include, for example, for transmucosal administration, detergents, bile salts, and fusidic acid derivatives.
  • the active ingredient can be formulated into aerosols, sprays, ointments, salves, gels, or creams as generally known in the art.
  • pharmaceutical compositions typically include ointments, creams, lotions, pastes, gels, sprays, aerosols, or oils.
  • Carriers which may be used include Vaseline, lanolin, polyethylene glycols, alcohols, transdermal enhancers, and combinations thereof.
  • Cosolvents and adjuvants may be added to the formulation.
  • cosolvents contain hydroxyl groups or other polar groups, for example, alcohols, such as isopropyl alcohol; glycols, such as propylene glycol, polyethyleneglycol, polypropylene glycol, glycol ether; glycerol; polyoxyethylene alcohols and polyoxyethylene fatty acid esters.
  • Adjuvants include, for example, surfactants such as, soya lecithin and oleic acid; sorbitan esters such as sorbitan trioleate; and polyvinylpyrrolidone.
  • compositions and methods of the invention are known in the art (see, e.g., Remington: The Science and Practice of Pharmacy (2003) 20 th ed., Mack Publishing Co., Easton, Pa.; Remington's Pharmaceutical Sciences (1990) 18 th ed., Mack Publishing Co., Easton, Pa.; The Merck Index (1996) 12 th ed., Merck Publishing Group, Whitehouse, N.J.; Pharmaceutical Principles of Solid Dosage Forms (1993), Technonic Publishing Co., Inc., Lancaster, Pa.; Ansel and Stoklosa, Pharmaceutical Calculations (2001) 11 th ed., Lippincott Williams & Wilkins, Baltimore, Md.; and Poznansky et al., Drug Delivery Systems (1980), R. L. Juliano, ed., Oxford, N.Y., pp. 253-315).
  • a “unit dosage form” as used herein refers to physically discrete units suited as unitary dosages for the subject to be treated; each unit containing a predetermined quantity optionally in association with a pharmaceutical carrier (excipient, diluent, vehicle or filling agent) which, when administered in one or more doses, is calculated to produce a desired effect (e.g., prophylactic or therapeutic effect).
  • Unit dosage forms may be within, for example, ampules and vials, which may include a liquid composition, or a composition in a freeze-dried or lyophilized state; a sterile liquid carrier, for example, can be added prior to administration or delivery in vivo.
  • Individual unit dosage forms can be included in multi-dose kits or containers. Pharmaceutical formulations can be packaged in single or multiple unit dosage form for ease of administration and uniformity of dosage.
  • kits with packaging material and one or more components therein typically includes a label or packaging insert including a description of the components or instructions for use in vitro, in vivo, or ex vivo, of the components therein.
  • a kit can contain a collection of such components, e.g., an AAV vector and optionally a second active, such as another compound, agent, drug or composition.
  • packaging material refers to a physical structure housing the components of the kit.
  • the packaging material can maintain the components sterilely, and can be made of material commonly used for such purposes (e.g., paper, corrugated fiber, glass, plastic, foil, ampules, vials, tubes, etc.).
  • Labels or inserts can include identifying information of one or more components therein, dose amounts, clinical pharmacology of the active ingredient(s) including mechanism of action, pharmacokinetics and pharmacodynamics. Labels or inserts can include information identifying manufacturer, lot numbers, manufacture location and date, expiration dates. Labels or inserts can include information identifying manufacturer information, lot numbers, manufacturer location and date. Labels or inserts can include information on a disease for which a kit component may be used. Labels or inserts can include instructions for the clinician or subject for using one or more of the kit components in a method, use, or treatment protocol or therapeutic regimen. Instructions can include dosage amounts, frequency or duration, and instructions for practicing any of the methods, uses, treatment protocols or prophylactic or therapeutic regimes described herein.
  • Labels or inserts can include information on any benefit that a component may provide, such as a prophylactic or therapeutic benefit. Labels or inserts can include information on potential adverse side effects, complications or reactions, such as warnings to the subject or clinician regarding situations where it would not be appropriate to use a particular composition. Adverse side effects or complications could also occur when the subject has, will be or is currently taking one or more other medications that may be incompatible with the composition, or the subject has, will be or is currently undergoing another treatment protocol or therapeutic regimen which would be incompatible with the composition and, therefore, instructions could include information regarding such incompatibilities.
  • Labels or inserts include “printed matter,” e.g., paper or cardboard, or separate or affixed to a component, a kit or packing material (e.g., a box), or attached to an ampule, tube or vial containing a kit component.
  • Labels or inserts can additionally include a computer readable medium, such as a bar-coded printed label, a disk, optical disk such as CD- or DVD-ROM/RAM, DVD, MP3, magnetic tape, or an electrical storage media such as RAM and ROM or hybrids of these such as magnetic/optical storage media, FLASH media or memory type cards.
  • GenBank citations and ATCC citations cited herein are incorporated by reference in their entirety. In case of conflict, the specification, including definitions, will control.
  • a polynucleotide includes a plurality of such polynucleotides, such as a plurality of genes.
  • Reference to a number with more (greater) or less than includes any number greater or less than the reference number, respectively.
  • a reference to less than 1,000 includes 999, 998, 997, etc. all the way down to the number one (1); and less than 100, includes 99, 98, 97, etc. all the way down to the number one (1).
  • Reference to a range of 1-50 therefore includes 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, etc., as well as 1.1, 1.2, 1.3, 1.4, 1.5, etc., 2.1, 2.2, 2.3, 2.4, 2.5, etc., and so forth.
  • Reference to a series of ranges includes ranges which combine the values of the boundaries of different ranges within the series.
  • 2-72 hours, 2-48 hours, 4-24 hours, 4-18 hours and 6-12 hours includes ranges of 2-6 hours, 2, 12 hours, 2-18 hours, 2-24 hours, etc., and 4-27 hours, 4-48 hours, 4-6 hours, etc.
  • the invention is generally disclosed herein using affirmative language to describe the numerous embodiments and aspects.
  • the invention also specifically includes embodiments in which particular subject matter is excluded, in full or in part, such as substances or materials, method steps and conditions, protocols, or procedures.
  • materials and/or method steps are excluded.
  • the invention is generally not expressed herein in terms of what the invention does not include aspects that are not expressly excluded in the invention are nevertheless disclosed herein.
  • This example includes a description of various materials and methods.
  • the dog is a HB dog from the University of North Carolina Chapel Hill colony carrying a missense mutation in the FIX gene (Evans et al., Proc Natl Acad Sci USA 86:10095 (1989)).
  • mice The in vivo studies in mice were performed using a construct expressing human FIX under the control of the ApoE-hAAT liver specific promoter.
  • the study in dogs used a nearly identical promoter and the canine FIX transgene.
  • vectors were delivered intravenously. In mice via the tail vein (a volume of 200 microliters per mouse was administered, vector was diluted in PBS). In dogs the vector was delivered via the saphenous vein.
  • FIX ELISA was used to measure FIX levels.
  • the human FIX ELISA antibody pair capture and secondary
  • an antibody pair also from Affinity Biologicals was used as described in Haurigot et al. ( Mol Ther 18:1318 (2010)).
  • 2V6.11 cells (ATCC) were used, which expressed the adenoviral gene E4 under the control of an inducible promoter.
  • Cells were seeded in a 96-well plate at a density of 1.25 ⁇ 10 4 cells/well and a 1:1000 dilution of ponasterone A (Invitrogen) was added to the medium to induce E4 expression.
  • ponasterone A Invitrogen
  • serial half-log dilutions of heat-inactivated test serum were mixed with medium containing virus.
  • virus concentration used in the assay was ⁇ 1 ⁇ 10 10 vg/ml for AAV2 and ⁇ 5.5 ⁇ 10 10 vg/ml for AAV5, 6, or 8.
  • virus concentration in the assay was between ⁇ 50 and 150-fold lower. Residual activity of the reporter transgene was measured using either a colorimetric assay (ssAAV-LacZ) or a luminometer (scAAV-Luc).
  • Anti-AAV capsid total IgG or Ig subclasses were measured with a capture assay; ELISA plates were coated with 5 ⁇ 10 10 capsid particles/ml of AAV empty capsids. Plates were blocked with 2% BSA, 0.05% Tween 20 in PBS for 2 hours at room temperature and serial dilutions of samples were loaded onto the wells and incubated overnight at 4° C. Biotin-conjugated anti-human IgG1, IgG2, IgG3, IgG4, or IgM antibody (Sigma) were used as detecting antibodies; streptavidin-HRP was the added for substrate detection. Ig concentration was determined against standard curves made with serial dilution of human purified IgG1, IgG2, IgG3, IgG4, or IgM (Sigma).
  • This example includes a description of human FIX gene transfer animal (Mice) studies and FIX expression after gene transfer.
  • Human FIX transgene product (protein) plasma levels in the mice were determined by ELISA at week 1, 2, and 4 post gene transfer, and are illustrated in FIG. 1 .
  • AAV-Rh74 showed the highest level of transgene expression in the animals.
  • This example includes a description of animal studies and data demonstrating effective AAV-Rh74 mediated delivery of FIX at therapeutic levels in hemophilia dogs.
  • hemophilia B dogs were infused intravenously (IV) though the saphenous vein with 3 ⁇ 10 12 vector genomes per kg of weight. Expression of the therapeutic FIX transgene was driven by a liver specific promoter. Vectors and FIX levels were monitored by ELISA. Canine FIX plasma levels are shown in FIG. 2 . AAV-Rh74 and AAV8 performed roughly equally in hemophilia B dogs, and both were superior to AAV6.
  • This example includes a description of studies showing the presence of anti-AAV neutralizing antibodies (NAb) in humans.
  • NAb anti-AAV neutralizing antibodies
  • This example includes a description of data showing production amounts of different AAV serotypes including AAV-Rh74.
  • AAV-Rh74 has a yield comparable to or greater than the other serotypes evaluated, namely AAV-8, AAV-dj, and AAV-2.
  • This example includes a description of data showing that AAVrh74 vector expressing human Factor IX (FIX) under the control of a liver-specific promoter administered to rhesus macaques led to production amounts of FIX in animals, and at higher levels than AAV8 vector administered at the same amount.
  • FIX human Factor IX
  • animals were administered either AAV8 or AAVrh74 at a dose of 2 ⁇ 10 12 vector genomes (vg)/kg of weight.
  • Vectors were either formulated in saline or in a mixture of vector and empty AAV capsid (denoted EC).
  • FIG. 4 is a histogram plot of the average (weeks 2 to 8) and standard error or the mean of human FIX measured by an ELISA that detects specifically human FIX in rhesus macaque plasma. Animals receiving the AAVrh74-FIX vector are shown in the last two bars towards the right margin. The data shows that animals receiving the AAVrh74 vectors (last two bars towards right margin) expressed the FIX transgene at higher levels compared to the other groups of animals injected at the same dose (black and grey bars). Average levels were compared using unpaired, two-tailed student t test.

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Cited By (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9255154B2 (en) 2012-05-08 2016-02-09 Alderbio Holdings, Llc Anti-PCSK9 antibodies and use thereof
US10287608B2 (en) 2017-04-03 2019-05-14 Encoded Therapeutics, Inc. Tissue selective transgene expression
US10323076B2 (en) 2013-10-03 2019-06-18 Modernatx, Inc. Polynucleotides encoding low density lipoprotein receptor
US10434088B2 (en) 2013-05-03 2019-10-08 Selecta Biosciences, Inc. Methods related to administering immunosuppressants and therapeutic macromolecules at a reduced pharmacodynamically effective dose
US10610606B2 (en) 2018-02-01 2020-04-07 Homology Medicines, Inc. Adeno-associated virus compositions for PAH gene transfer and methods of use thereof
CN111225677A (zh) * 2017-07-17 2020-06-02 星火治疗股份有限公司 单采血液分离方法和用途
WO2020167996A1 (en) * 2019-02-12 2020-08-20 Rocket Pharmaceuticals, Ltd. Gene therapy vectors for treatment of danon disease
WO2021041546A1 (en) 2019-08-27 2021-03-04 Vertex Pharmaceuticals Incorporated Compositions and methods for treatment of disorders associated with repetitive dna
US20210214751A1 (en) * 2015-10-21 2021-07-15 The United States Of America, As Represented By The Secretary, Dept. Of Health And Human Services Codon-optimized reduced-size atp7a cdna and uses for treatment of copper transport disorders
US11235057B2 (en) 2011-04-29 2022-02-01 Selecta Biosciences, Inc. Methods for providing polymeric synthetic nanocarriers for generating antigen-specific tolerance immune responses
WO2022056000A1 (en) 2020-09-09 2022-03-17 Vertex Pharmaceuticals Incorporated Compositions and methods for treatment of duchenne muscular dystrophy
US20220089670A1 (en) * 2018-12-28 2022-03-24 University Of Rochester Gene Therapy for BEST1 Dominant Mutations
US11306329B2 (en) 2018-02-19 2022-04-19 City Of Hope Adeno-associated virus compositions for restoring F8 gene function and methods of use thereof
WO2022098933A1 (en) 2020-11-06 2022-05-12 Vertex Pharmaceuticals Incorporated Compositions and methods for treatment of dm1 with slucas9 and sacas9
US11426451B2 (en) 2017-03-11 2022-08-30 Selecta Biosciences, Inc. Methods and compositions related to combined treatment with antiinflammatories and synthetic nanocarriers comprising an immunosuppressant
WO2022182957A1 (en) 2021-02-26 2022-09-01 Vertex Pharmaceuticals Incorporated Compositions and methods for treatment of myotonic dystrophy type 1 with crispr/sacas9
WO2022182959A1 (en) 2021-02-26 2022-09-01 Vertex Pharmaceuticals Incorporated Compositions and methods for treatment of myotonic dystrophy type 1 with crispr/slucas9
US11434502B2 (en) 2017-10-16 2022-09-06 Voyager Therapeutics, Inc. Treatment of amyotrophic lateral sclerosis (ALS)
WO2022204476A1 (en) 2021-03-26 2022-09-29 The Board Of Regents Of The University Of Texas System Nucleotide editing to reframe dmd transcripts by base editing and prime editing
WO2022229851A1 (en) 2021-04-26 2022-11-03 Crispr Therapeutics Ag Compositions and methods for using slucas9 scaffold sequences
WO2022234519A1 (en) 2021-05-05 2022-11-10 Crispr Therapeutics Ag Compositions and methods for using sacas9 scaffold sequences
US11542506B2 (en) 2014-11-14 2023-01-03 Voyager Therapeutics, Inc. Compositions and methods of treating amyotrophic lateral sclerosis (ALS)
WO2023018637A1 (en) 2021-08-09 2023-02-16 Vertex Pharmaceuticals Incorporated Gene editing of regulatory elements
US11603542B2 (en) 2017-05-05 2023-03-14 Voyager Therapeutics, Inc. Compositions and methods of treating amyotrophic lateral sclerosis (ALS)
WO2023039444A2 (en) 2021-09-08 2023-03-16 Vertex Pharmaceuticals Incorporated Precise excisions of portions of exon 51 for treatment of duchenne muscular dystrophy
US11633422B2 (en) 2014-09-07 2023-04-25 Selecta Biosciences, Inc. Methods and compositions for attenuating anti-viral transfer vector immune responses
US11634728B2 (en) 2017-12-29 2023-04-25 Helixmith Co., Ltd Adeno-associated virus (AAV) vector having hybrid HGF gene introduced thereto
WO2023070019A1 (en) 2021-10-21 2023-04-27 Vertex Pharmaceuticals Incorporated Hypoimmune cells
US11690898B2 (en) 2015-09-24 2023-07-04 Biomarin Pharmaceutical Inc. Adeno-associated virus Factor VIII vectors, associated viral particles and therapeutic formulations comprising the same
US11707536B2 (en) 2019-01-16 2023-07-25 Takeda Pharmaceutical Company Limited Viral vectors encoding recombinant FVIII variants with increased expression for gene therapy of hemophilia A
US20230233709A1 (en) * 2017-03-01 2023-07-27 The Trustees Of The University Of Pennsylvania Gene therapy for ocular disorders
WO2023161648A1 (en) * 2022-02-25 2023-08-31 Babraham Institute Novel use and method comprising il-2 and a tissue- or organ-specific targeting moiety
WO2023172926A1 (en) 2022-03-08 2023-09-14 Vertex Pharmaceuticals Incorporated Precise excisions of portions of exons for treatment of duchenne muscular dystrophy
WO2023172927A1 (en) 2022-03-08 2023-09-14 Vertex Pharmaceuticals Incorporated Precise excisions of portions of exon 44, 50, and 53 for treatment of duchenne muscular dystrophy
WO2023205606A1 (en) 2022-04-18 2023-10-26 Vertex Pharmaceuticals Incorporated Compositions and methods for enhancing aav therapy and decreasing tropism of aav to the liver
WO2024020352A1 (en) 2022-07-18 2024-01-25 Vertex Pharmaceuticals Incorporated Tandem guide rnas (tg-rnas) and their use in genome editing
US11883506B2 (en) 2020-08-07 2024-01-30 Spacecraft Seven, Llc Plakophilin-2 (PKP2) gene therapy using AAV vector
US11883470B2 (en) 2016-07-25 2024-01-30 The Trustees Of The University Of Pennsylvania Compositions comprising a lecithin cholesterol acyltransferase variant and uses thereof
US11952585B2 (en) 2020-01-13 2024-04-09 Homology Medicines, Inc. Methods of treating phenylketonuria
RU2822925C2 (ru) * 2019-02-12 2024-07-16 Спейскрафт Севен, Ллк Векторы для генной терапии для лечения болезни данона
US12071633B2 (en) 2020-10-13 2024-08-27 Kriya Therapeutics, Inc. Viral vector constructs for delivery of nucleic acids encoding cytokines and uses thereof for treating cancer
US12076420B2 (en) 2020-05-27 2024-09-03 Homology Medicines, Inc. Adeno-associated virus compositions for restoring PAH gene function and methods of use thereof
US12083188B2 (en) 2017-12-01 2024-09-10 Encoded Therapeutics, Inc. Engineered DNA binding proteins

Families Citing this family (94)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ578982A (en) 2001-11-13 2011-03-31 Univ Pennsylvania A method of detecting and/or identifying adeno-associated virus (AAV) sequences and isolating novel sequences identified thereby
US9217155B2 (en) 2008-05-28 2015-12-22 University Of Massachusetts Isolation of novel AAV'S and uses thereof
US8734809B2 (en) 2009-05-28 2014-05-27 University Of Massachusetts AAV's and uses thereof
EP2561073B1 (en) 2010-04-23 2016-08-24 University of Massachusetts Cns targeting aav vectors and methods of use thereof
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WO2013078400A1 (en) 2011-11-22 2013-05-30 The Children's Hospital Of Philadelphia Virus vectors for highly efficient transgene delivery
JP2015529685A (ja) 2012-09-17 2015-10-08 ザ・リサーチ・インスティテュート・アット・ネイションワイド・チルドレンズ・ホスピタルＴｈｅ Ｒｅｓｅａｒｃｈ Ｉｎｓｔｉｔｕｔｅ Ａｔｎａｔｉｏｎｗｉｄｅ Ｃｈｉｌｄｒｅｎ’Ｓ Ｈｏｓｐｉｔａｌ 筋萎縮性側索硬化症の処置のための組成物および方法
BR112015021884A8 (pt) * 2013-03-15 2019-11-26 Childrens Hospital Philadelphia vetores de plasmídeo recombinantes, partícula viral avv ou pluralidade de partículas virais, seus métodos de produção e seus usos, e composição farmacêutica
EP3024498B1 (en) * 2013-07-22 2019-12-04 The Children's Hospital of Philadelphia Variant aav and compositions, methods and uses for gene transfer to cells, organs and tissues
EP3065784A4 (en) 2013-11-05 2017-05-10 The Research Institute at Nationwide Children's Hospital COMPOSITIONS AND METHODS FOR INHIBITING NF- kB AND SOD-1 TO TREAT AMYOTROPHIC LATERAL SCLEROSIS
US10072251B2 (en) 2014-02-19 2018-09-11 University Of Massachusetts Recombinant AAVS having useful transcytosis properties
EP4410805A2 (en) 2014-03-18 2024-08-07 University of Massachusetts Raav-based compositions and methods for treating amyotrophic lateral sclerosis
DK3628334T5 (da) * 2014-03-21 2024-09-02 Genzyme Corp Genterapi til behandling af retinitis pigmentosa
JP6741590B2 (ja) 2014-04-25 2020-08-19 ザ・トラステイーズ・オブ・ザ・ユニバーシテイ・オブ・ペンシルベニア コレステロールレベルを低下させるためのｌｄｌｒ変異体および組成物中でのそれらの使用
WO2015164786A1 (en) 2014-04-25 2015-10-29 University Of Massachusetts Recombinant aav vectors useful for reducing immunity against transgene products
US10689653B2 (en) 2014-06-03 2020-06-23 University Of Massachusetts Compositions and methods for modulating dysferlin expression
US10577627B2 (en) 2014-06-09 2020-03-03 Voyager Therapeutics, Inc. Chimeric capsids
CN105396143B (zh) * 2014-09-01 2020-06-26 江苏命码生物科技有限公司 埃博拉病毒特异性的miRNA以及通过miRNA抑制埃博拉病毒的方法
US10370432B2 (en) 2014-10-03 2019-08-06 University Of Massachusetts Heterologous targeting peptide grafted AAVS
US10711270B2 (en) 2014-10-03 2020-07-14 University Of Massachusetts High efficiency library-identified AAV vectors
EP3209311B1 (en) 2014-10-21 2024-03-06 University of Massachusetts Recombinant aav variants and uses thereof
MX2017005834A (es) 2014-11-05 2017-11-17 Voyager Therapeutics Inc Polinucleotidos aad para el tratamiento de la enfermedad de parkinson.
GB201420139D0 (en) 2014-11-12 2014-12-24 Ucl Business Plc Factor IX gene therapy
RU2749882C2 (ru) 2014-11-14 2021-06-18 Вояджер Терапьютикс, Инк. Модулирующие полинуклеотиды
US11697825B2 (en) 2014-12-12 2023-07-11 Voyager Therapeutics, Inc. Compositions and methods for the production of scAAV
EP3256170B1 (en) 2015-02-13 2020-09-23 University of Massachusetts Compositions and methods for transient delivery of nucleases
CA3021949C (en) 2015-04-24 2023-10-17 University Of Massachusetts Modified aav constructs and uses thereof
JP6745873B2 (ja) 2015-05-22 2020-08-26 ドミトリエヴィッチ ゲンキン，ドミトリー 神経変性における治療標的としての細胞外ｄｎａ
CN108138159A (zh) 2015-06-23 2018-06-08 费城儿童医院 经修饰的因子ix、以及用于基因转移到细胞、器官和组织的组合物、方法和用途
CA3002980A1 (en) 2015-10-22 2017-04-27 University Of Massachusetts Prostate-targeting adeno-associated virus serotype vectors
US11253576B2 (en) 2015-10-22 2022-02-22 University Of Massachusetts Methods and compositions for treating metabolic imbalance in neurodegenerative disease
JP6695426B2 (ja) 2015-11-13 2020-05-20 バクスアルタ インコーポレイテッド 組換えｆｖｉｉｉ変異型をコードする血友病ａ遺伝子治療用高発現ウイルスベクター
BR112018009717B1 (pt) 2015-11-13 2021-12-14 Takeda Pharmaceutical Company Limited Polinucleotídeo, vetor de vírus adeno-associado, partícula de um vírus adeno-associado, métodos para produzir uma partícula de vírus adeno-associado e para transduzir uma célula hospedeira, e, uso de uma partícula de vírus adeno-associado
RU2766583C2 (ru) * 2015-12-01 2022-03-15 Спарк Терапьютикс, Инк. Масштабируемые способы получения рекомбинантного вектора на основе аденоассоциированного вируса (aav) в системе бессывороточной суспензионной культуры клеток, подходящего для клинического применения
CA3006569A1 (en) 2015-12-02 2017-06-08 Voyager Therapeutics, Inc. Assays for the detection of aav neutralizing antibodies
WO2017100682A1 (en) * 2015-12-11 2017-06-15 The Trustees Of The University Of Pennsylvania Gene therapy for treating familial hypercholesterolemia
CA3011939A1 (en) 2016-02-02 2017-08-10 University Of Massachusetts Method to enhance the efficiency of systemic aav gene delivery to the central nervous system
US11060088B2 (en) 2016-02-12 2021-07-13 University Of Massachusetts Anti-angiogenic miRNA therapeutics for inhibiting corneal neovascularization
SG11201808398PA (en) * 2016-03-30 2018-10-30 Spark Therapeutics Inc Cell line for recombinant protein and/or viral vector production
EP3440210A4 (en) 2016-04-05 2019-11-27 University of Massachusetts COMPOSITIONS AND METHODS FOR SELECTIVE INHIBITION OF EXPRESSION OF GRAINHEAD PROTEIN
LT3442600T (lt) * 2016-04-15 2024-05-27 Research Institute At Nationwide Children's Hospital Su adeno virusu susijusio viruso vektoriaus iš β-sarkoglikano ir mikro- rnr-29 pristatymas ir raumenų distrofijos gydymas
US11413356B2 (en) 2016-04-15 2022-08-16 University Of Massachusetts Methods and compositions for treating metabolic imbalance
US11299751B2 (en) 2016-04-29 2022-04-12 Voyager Therapeutics, Inc. Compositions for the treatment of disease
EP3448874A4 (en) 2016-04-29 2020-04-22 Voyager Therapeutics, Inc. COMPOSITIONS FOR TREATING A DISEASE
FI3445773T3 (fi) 2016-05-13 2023-03-30 4D Molecular Therapeutics Inc Adenoassosioituneen viruksen kapsidimuunnoksia ja niiden käyttömenetelmiä
JP7220080B2 (ja) 2016-05-18 2023-02-09 ボイジャー セラピューティクス インコーポレイテッド ハンチントン病治療組成物及び方法
RU2758488C2 (ru) 2016-05-18 2021-10-28 Вояджер Терапьютикс, Инк. Модулирующие полинуклеотиды
US11882815B2 (en) 2016-06-15 2024-01-30 University Of Massachusetts Recombinant adeno-associated viruses for delivering gene editing molecules to embryonic cells
EP3491008A2 (en) 2016-07-26 2019-06-05 BioMarin Pharmaceutical Inc. Novel adeno-associated virus capsid proteins
CN110225975A (zh) 2016-08-23 2019-09-10 阿库斯股份有限公司 用于治疗人受试者中非年龄相关的听力损害的组合物和方法
CN106344932B (zh) * 2016-08-26 2019-12-27 首都医科大学附属北京同仁医院 一种用于提高视网膜退行性疾病基因治疗效果的组合物及其应用
EP3506817A4 (en) 2016-08-30 2020-07-22 The Regents of The University of California METHOD FOR BIOMEDICAL TARGETING AND RELEASE, AND DEVICES AND SYSTEMS FOR IMPLEMENTING THEM
US10457940B2 (en) 2016-09-22 2019-10-29 University Of Massachusetts AAV treatment of Huntington's disease
AU2017341849B2 (en) 2016-10-13 2024-03-21 University Of Massachusetts AAV capsid designs
WO2018082093A1 (en) * 2016-11-07 2018-05-11 Wuhan Institute Of Virology, Chinese Academy Of Sciences Anterograde monosynaptic transneuronal tracer system
WO2018131551A1 (ja) 2017-01-13 2018-07-19 学校法人自治医科大学 肝臓ゲノム上の凝固関連因子遺伝子を破壊するためのａａｖベクター
EP3595688A4 (en) 2017-02-20 2020-12-30 The Trustees Of The University Of Pennsylvania GENE THERAPY TO TREAT FAMILY HYPERCHOLESTERINEMIA
JP2020513811A (ja) * 2017-03-17 2020-05-21 リサーチ インスティチュート アット ネイションワイド チルドレンズ ホスピタル 筋ジストロフィーを治療するための筋肉特異的マイクロジストロフィンのアデノ随伴ウイルスベクター送達
WO2018204803A1 (en) 2017-05-05 2018-11-08 Voyager Therapeutics, Inc. Compositions and methods of treating huntington's disease
US11859179B2 (en) 2017-05-09 2024-01-02 University Of Massachusetts Methods of treating amyotrophic lateral sclerosis (ALS)
CN110944674B (zh) 2017-05-19 2024-07-19 编码治疗公司 高活性调控元件
CN110945127B (zh) 2017-05-22 2024-07-12 武田药品工业株式会社 用于血友病b的基因疗法的编码具有增加的表达的重组fix的病毒载体
JOP20190269A1 (ar) 2017-06-15 2019-11-20 Voyager Therapeutics Inc بولي نوكليوتيدات aadc لعلاج مرض باركنسون
JP7229989B2 (ja) 2017-07-17 2023-02-28 ボイジャー セラピューティクス インコーポレイテッド 軌道アレイガイドシステム
EP3662060A2 (en) 2017-08-03 2020-06-10 Voyager Therapeutics, Inc. Compositions and methods for delivery of aav
US20210130845A1 (en) * 2017-09-08 2021-05-06 Poseida Therapeutics, Inc. Compositions and methods for chimeric ligand receptor (clr)-mediated conditional gene expression
RU2770922C2 (ru) 2017-09-20 2022-04-25 4Д Молекьюлар Терапьютикс Инк. Капсиды вариантов аденоассоциированных вирусов и методы их применения
AU2018338188A1 (en) 2017-09-22 2020-04-02 University Of Massachusetts SOD1 dual expression vectors and uses thereof
EP3697908A1 (en) 2017-10-16 2020-08-26 Voyager Therapeutics, Inc. Treatment of amyotrophic lateral sclerosis (als)
CN107760719B (zh) * 2017-10-24 2020-09-22 北京领柯生物科技有限公司 柯萨奇病毒在过继免疫基因递送系统中的应用
US11766489B2 (en) 2017-11-27 2023-09-26 4D Molecular Therapeutics, Inc. Adeno-associated virus variant capsids and use for inhibiting angiogenesis
US11905533B2 (en) 2017-12-19 2024-02-20 The University Of North Carolina At Chapel Hill Methods and compositions for delivery of viral vectors across the blood-brain barrier
WO2019143272A1 (en) * 2018-01-16 2019-07-25 Cls Therapeutics Limited Treatment of diseases by liver expression of an enzyme which has a deoxyribonuclease (dnase) activity
JP7374119B2 (ja) 2018-04-05 2023-11-06 ジェネトン 減少した肝臓向性を有するＡＡＶ９とＡＡＶｒｈ７４とのハイブリッド組換えアデノ随伴ウイルス血清型
KR20210008501A (ko) 2018-05-09 2021-01-22 바이오마린 파머수티컬 인크. 페닐케톤뇨증을 치료하는 방법
TW202005978A (zh) 2018-05-14 2020-02-01 美商拜奧馬林製藥公司 新穎肝靶向腺相關病毒載體
WO2020018419A1 (en) 2018-07-16 2020-01-23 Baxalta Incorporated Gene therapy of hemophilia a using viral vectors encoding recombinant fviii variants with increased expression
BR112021016501A2 (pt) 2019-02-25 2021-10-26 Novartis Ag Composições e métodos para tratar distrofia cristalina de bietti
WO2020174369A2 (en) 2019-02-25 2020-09-03 Novartis Ag Compositions and methods to treat bietti crystalline dystrophy
CN109999182B (zh) * 2019-03-29 2023-03-07 四川大学华西医院 凝血因子在制备抗肿瘤药物中的应用
US20230340078A1 (en) 2019-11-14 2023-10-26 Biomarin Pharmaceutical Inc. Treatment of hereditary angioedema with liver-specific gene therapy vectors
CN113025618B (zh) * 2019-12-24 2024-02-06 朗信启昇(苏州)生物制药有限公司 一种x连锁遗传性视网膜劈裂症的基因治疗方案与应用
AU2021225035A1 (en) 2020-02-21 2022-10-13 Akouos, Inc. Compositions and methods for treating non-age-associated hearing impairment in a human subject
TW202144575A (zh) 2020-04-03 2021-12-01 美商拜奧馬林製藥公司 使用ａａｖ及治療調配物之苯酮尿症治療
EP4165076A1 (en) * 2020-06-15 2023-04-19 Sarepta Therapeutics, Inc. Adeno-associated virus antibodies and fragments thereof
CN111500635B (zh) * 2020-07-02 2020-10-09 北京大学第三医院（北京大学第三临床医学院） 一种包含携带核酸分子的载体的试剂盒
CN111876432B (zh) * 2020-07-29 2022-10-28 舒泰神（北京）生物制药股份有限公司 一组肝靶向新型腺相关病毒的获得及其应用
KR20240014477A (ko) 2021-05-28 2024-02-01 상하이 레제네리드 테라피즈 컴퍼니 리미티드 변이체 캡시드를 갖는 재조합 아데노-연관 바이러스 및 이의 응용
WO2023280175A1 (en) * 2021-07-06 2023-01-12 National Institute Of Biological Sciences, Beijing Methods for treating complex i deficiencies or cancers by modulating gro3p biosynthesis
AR127217A1 (es) 2021-10-01 2023-12-27 Biomarin Pharm Inc Tratamiento de angioedema hereditario con vectores de genoterapia de aav y formulaciones terapéuticas
EP4442830A1 (en) 2021-11-29 2024-10-09 Shanghai Regenelead Therapies Co., Ltd. Aadc/gdnf polynucleotide, and use thereof in treating parkinson's disease
AU2023220237A1 (en) 2022-02-21 2024-08-15 Shanghai Regenelead Therapies Co., Ltd Vegf-binding molecule and pharmaceutical use thereof
CN118460618A (zh) * 2022-04-19 2024-08-09 康霖生物科技（杭州）有限公司 一种用于遗传性凝血因子缺乏病治疗的核酸构建体
WO2024064856A1 (en) 2022-09-22 2024-03-28 Biomarin Pharmaceutical Inc. Treatment of cardiomyopathy with aav gene therapy vectors

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140323956A1 (en) * 2011-11-23 2014-10-30 Nationwide Children's Hospital, Inc. Recombinant adeno-associated virus delivery of alpha-sarcoglycan polynucleotides

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6156303A (en) 1997-06-11 2000-12-05 University Of Washington Adeno-associated virus (AAV) isolates and AAV vectors derived therefrom
US6468524B1 (en) 2000-03-22 2002-10-22 The United States Of America, As Represented By The Secretary Of The Department Of Health And Human Services AAV4 vector and uses thereof
NZ578982A (en) * 2001-11-13 2011-03-31 Univ Pennsylvania A method of detecting and/or identifying adeno-associated virus (AAV) sequences and isolating novel sequences identified thereby
US8999678B2 (en) * 2005-04-07 2015-04-07 The Trustees Of The University Of Pennsylvania Method of increasing the function of an AAV vector
US7588772B2 (en) * 2006-03-30 2009-09-15 Board Of Trustees Of The Leland Stamford Junior University AAV capsid library and AAV capsid proteins
EP2561073B1 (en) * 2010-04-23 2016-08-24 University of Massachusetts Cns targeting aav vectors and methods of use thereof
CA2814143C (en) * 2010-10-12 2020-09-08 The Children's Hospital Of Philadelphia Methods and compositions for treating hemophilia b
CN108138159A (zh) * 2015-06-23 2018-06-08 费城儿童医院 经修饰的因子ix、以及用于基因转移到细胞、器官和组织的组合物、方法和用途

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140323956A1 (en) * 2011-11-23 2014-10-30 Nationwide Children's Hospital, Inc. Recombinant adeno-associated virus delivery of alpha-sarcoglycan polynucleotides

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Fumoto et al, Targeted Gene Delivery:Importance of Administration Routes, Intech, 2013, pages 3-31. *
Katz et al, Cardiac Gene Therapy: Optimization of Gene Delivery Techniques In Vivo, HUMAN GENE THERAPY 21:371–380 (April 2010) *

Cited By (56)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11235057B2 (en) 2011-04-29 2022-02-01 Selecta Biosciences, Inc. Methods for providing polymeric synthetic nanocarriers for generating antigen-specific tolerance immune responses
US11779641B2 (en) 2011-04-29 2023-10-10 Selecta Biosciences, Inc. Tolerogenic synthetic nanocarriers for allergy therapy
US11717569B2 (en) 2011-04-29 2023-08-08 Selecta Biosciences, Inc. Tolerogenic synthetic nanocarriers
US10259885B2 (en) 2012-05-08 2019-04-16 Alderbio Holdings Llc Anti-PCSK9 antibodies and use thereof
US9255154B2 (en) 2012-05-08 2016-02-09 Alderbio Holdings, Llc Anti-PCSK9 antibodies and use thereof
US11298342B2 (en) 2013-05-03 2022-04-12 Selecta Biosciences, Inc. Methods providing a therapeutic macromolecule and synthetic nanocarriers comprising immunosuppressant locally and concomitantly to reduce both type I and type IV hypersensitivity
US10434088B2 (en) 2013-05-03 2019-10-08 Selecta Biosciences, Inc. Methods related to administering immunosuppressants and therapeutic macromolecules at a reduced pharmacodynamically effective dose
US10668053B2 (en) 2013-05-03 2020-06-02 Selecta Biosciences, Inc. Tolerogenic synthetic nanocarriers to reduce or prevent anaphylaxis in response to a non-allergenic antigen
US10323076B2 (en) 2013-10-03 2019-06-18 Modernatx, Inc. Polynucleotides encoding low density lipoprotein receptor
US11633422B2 (en) 2014-09-07 2023-04-25 Selecta Biosciences, Inc. Methods and compositions for attenuating anti-viral transfer vector immune responses
US11542506B2 (en) 2014-11-14 2023-01-03 Voyager Therapeutics, Inc. Compositions and methods of treating amyotrophic lateral sclerosis (ALS)
US11690898B2 (en) 2015-09-24 2023-07-04 Biomarin Pharmaceutical Inc. Adeno-associated virus Factor VIII vectors, associated viral particles and therapeutic formulations comprising the same
US20210214751A1 (en) * 2015-10-21 2021-07-15 The United States Of America, As Represented By The Secretary, Dept. Of Health And Human Services Codon-optimized reduced-size atp7a cdna and uses for treatment of copper transport disorders
US11883470B2 (en) 2016-07-25 2024-01-30 The Trustees Of The University Of Pennsylvania Compositions comprising a lecithin cholesterol acyltransferase variant and uses thereof
US20230233709A1 (en) * 2017-03-01 2023-07-27 The Trustees Of The University Of Pennsylvania Gene therapy for ocular disorders
US11426451B2 (en) 2017-03-11 2022-08-30 Selecta Biosciences, Inc. Methods and compositions related to combined treatment with antiinflammatories and synthetic nanocarriers comprising an immunosuppressant
US10519465B2 (en) 2017-04-03 2019-12-31 Encoded Therapeutics, Inc. Tissue selective transgene expression
US10287607B2 (en) 2017-04-03 2019-05-14 Encoded Therapeutics, Inc. Tissue selective transgene expression
US10287608B2 (en) 2017-04-03 2019-05-14 Encoded Therapeutics, Inc. Tissue selective transgene expression
US11603542B2 (en) 2017-05-05 2023-03-14 Voyager Therapeutics, Inc. Compositions and methods of treating amyotrophic lateral sclerosis (ALS)
CN111225677A (zh) * 2017-07-17 2020-06-02 星火治疗股份有限公司 单采血液分离方法和用途
US11434502B2 (en) 2017-10-16 2022-09-06 Voyager Therapeutics, Inc. Treatment of amyotrophic lateral sclerosis (ALS)
US12116589B2 (en) 2017-10-16 2024-10-15 Voyager Therapeutics, Inc. Treatment of amyotrophic lateral sclerosis (ALS)
US12083188B2 (en) 2017-12-01 2024-09-10 Encoded Therapeutics, Inc. Engineered DNA binding proteins
US11634728B2 (en) 2017-12-29 2023-04-25 Helixmith Co., Ltd Adeno-associated virus (AAV) vector having hybrid HGF gene introduced thereto
US11951183B2 (en) 2018-02-01 2024-04-09 Homology Medicines, Inc. Adeno-associated virus compositions for PAH gene transfer and methods of use thereof
US12064486B2 (en) 2018-02-01 2024-08-20 Homology Medicines, Inc. Adeno-associated virus compositions for PAH gene transfer and methods of use thereof
US10610606B2 (en) 2018-02-01 2020-04-07 Homology Medicines, Inc. Adeno-associated virus compositions for PAH gene transfer and methods of use thereof
US11891619B2 (en) 2018-02-19 2024-02-06 City Of Hope Adeno-associated virus compositions for restoring F8 gene function and methods of use thereof
US11306329B2 (en) 2018-02-19 2022-04-19 City Of Hope Adeno-associated virus compositions for restoring F8 gene function and methods of use thereof
US20220089670A1 (en) * 2018-12-28 2022-03-24 University Of Rochester Gene Therapy for BEST1 Dominant Mutations
US11707536B2 (en) 2019-01-16 2023-07-25 Takeda Pharmaceutical Company Limited Viral vectors encoding recombinant FVIII variants with increased expression for gene therapy of hemophilia A
CN113508130A (zh) * 2019-02-12 2021-10-15 太空飞船七有限责任公司 用于治疗达农病的基因治疗载体
RU2822925C2 (ru) * 2019-02-12 2024-07-16 Спейскрафт Севен, Ллк Векторы для генной терапии для лечения болезни данона
WO2020167996A1 (en) * 2019-02-12 2020-08-20 Rocket Pharmaceuticals, Ltd. Gene therapy vectors for treatment of danon disease
WO2021041546A1 (en) 2019-08-27 2021-03-04 Vertex Pharmaceuticals Incorporated Compositions and methods for treatment of disorders associated with repetitive dna
US11952585B2 (en) 2020-01-13 2024-04-09 Homology Medicines, Inc. Methods of treating phenylketonuria
US12076420B2 (en) 2020-05-27 2024-09-03 Homology Medicines, Inc. Adeno-associated virus compositions for restoring PAH gene function and methods of use thereof
US11883506B2 (en) 2020-08-07 2024-01-30 Spacecraft Seven, Llc Plakophilin-2 (PKP2) gene therapy using AAV vector
WO2022056000A1 (en) 2020-09-09 2022-03-17 Vertex Pharmaceuticals Incorporated Compositions and methods for treatment of duchenne muscular dystrophy
US12071633B2 (en) 2020-10-13 2024-08-27 Kriya Therapeutics, Inc. Viral vector constructs for delivery of nucleic acids encoding cytokines and uses thereof for treating cancer
WO2022098933A1 (en) 2020-11-06 2022-05-12 Vertex Pharmaceuticals Incorporated Compositions and methods for treatment of dm1 with slucas9 and sacas9
WO2022182957A1 (en) 2021-02-26 2022-09-01 Vertex Pharmaceuticals Incorporated Compositions and methods for treatment of myotonic dystrophy type 1 with crispr/sacas9
WO2022182959A1 (en) 2021-02-26 2022-09-01 Vertex Pharmaceuticals Incorporated Compositions and methods for treatment of myotonic dystrophy type 1 with crispr/slucas9
WO2022204476A1 (en) 2021-03-26 2022-09-29 The Board Of Regents Of The University Of Texas System Nucleotide editing to reframe dmd transcripts by base editing and prime editing
WO2022229851A1 (en) 2021-04-26 2022-11-03 Crispr Therapeutics Ag Compositions and methods for using slucas9 scaffold sequences
WO2022234519A1 (en) 2021-05-05 2022-11-10 Crispr Therapeutics Ag Compositions and methods for using sacas9 scaffold sequences
WO2023018637A1 (en) 2021-08-09 2023-02-16 Vertex Pharmaceuticals Incorporated Gene editing of regulatory elements
WO2023039444A2 (en) 2021-09-08 2023-03-16 Vertex Pharmaceuticals Incorporated Precise excisions of portions of exon 51 for treatment of duchenne muscular dystrophy
WO2023070019A1 (en) 2021-10-21 2023-04-27 Vertex Pharmaceuticals Incorporated Hypoimmune cells
WO2023161648A1 (en) * 2022-02-25 2023-08-31 Babraham Institute Novel use and method comprising il-2 and a tissue- or organ-specific targeting moiety
WO2023172927A1 (en) 2022-03-08 2023-09-14 Vertex Pharmaceuticals Incorporated Precise excisions of portions of exon 44, 50, and 53 for treatment of duchenne muscular dystrophy
WO2023172926A1 (en) 2022-03-08 2023-09-14 Vertex Pharmaceuticals Incorporated Precise excisions of portions of exons for treatment of duchenne muscular dystrophy
WO2023205606A1 (en) 2022-04-18 2023-10-26 Vertex Pharmaceuticals Incorporated Compositions and methods for enhancing aav therapy and decreasing tropism of aav to the liver
WO2024020352A1 (en) 2022-07-18 2024-01-25 Vertex Pharmaceuticals Incorporated Tandem guide rnas (tg-rnas) and their use in genome editing
US12123002B2 (en) 2022-12-20 2024-10-22 Voyager Therapeutics, Inc. Compositions and methods of treating amyotrophic lateral sclerosis (ALS)

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