Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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  • 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
  • C12N15/87—Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
  • C12N15/90—Stable introduction of foreign DNA into chromosome
  • C12N15/902—Stable introduction of foreign DNA into chromosome using homologous recombination
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K38/00—Medicinal preparations containing peptides
  • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
  • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
  • A61K38/1703—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
  • A61K38/1709—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
• • 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
  • A61K48/005—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy characterised by an aspect of the 'active' part of the composition delivered, i.e. the nucleic acid delivered
  • A61K48/0058—Nucleic acids adapted for tissue specific expression, e.g. having tissue specific promoters as part of a contruct
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P27/00—Drugs for disorders of the senses
  • A61P27/02—Ophthalmic agents
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
  • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
  • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
  • C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
  • C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
• • C—CHEMISTRY; METALLURGY
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  • 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
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
  • A01K2217/00—Genetically modified animals
  • A01K2217/07—Animals genetically altered by homologous recombination
  • A01K2217/075—Animals genetically altered by homologous recombination inducing loss of function, i.e. knock out
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
  • A01K2227/00—Animals characterised by species
  • A01K2227/10—Mammal
  • A01K2227/105—Murine
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
  • A01K2267/00—Animals characterised by purpose
  • A01K2267/03—Animal model, e.g. for test or diseases
  • A01K2267/0306—Animal model for genetic diseases
• • C—CHEMISTRY; METALLURGY
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  • 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
• • C—CHEMISTRY; METALLURGY
  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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  • C12N2800/00—Nucleic acids vectors
  • C12N2800/40—Systems of functionally co-operating vectors
• • C—CHEMISTRY; METALLURGY
  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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  • C12N2840/00—Vectors comprising a special translation-regulating system
  • C12N2840/44—Vectors comprising a special translation-regulating system being a specific part of the splice mechanism, e.g. donor, acceptor
  • C12N2840/445—Vectors comprising a special translation-regulating system being a specific part of the splice mechanism, e.g. donor, acceptor for trans-splicing, e.g. polypyrimidine tract, branch point splicing

Definitions

• Nonsyndromic deafness is a form of hearing loss that is generally caused by defects or damage to the inner ear and/or middle ear. Mutations in the OTOF gene, which encodes the protein Otoferlin, are thought to cause a type of nonsyndromic deafness called Deafness, Autosomal Recessive 9 (DFNB9). Treatment of DFNB9 and other similar forms of deafness currently involves using cochlear implants for severe or profound hearing loss and hearing aids for milder forms of hearing loss. There remains a need for alternative treatment forms that do not rely on or rely less heavily on electronic devices for restoring hearing.
• DFNB9 Autosomal Recessive 9
• compositions and methods for expressing Otoferlin e.g., in a cell or subject.
• AAV adeno-associated virus
• the disclosure provides a method of increasing expression of Otoferlin in a cell, the method comprising contacting the cell with a first AAV particle comprising a first polynucleotide; and contacting the cell with a second AAV particle comprising a second polynucleotide, wherein the first polynucleotide comprises inverted terminal repeat sequences flanking an expression cassette containing, from 5' to 3' : (a) a promoter, (b) a partial coding sequence that encodes an N-terminal portion of an Otoferlin polypeptide, (c) a splice donor site, and (d) a first region of homology containing a sequence that is homologous to a sequence in the second polynucleotide, and the second polynucleotide comprises inverted terminal repeat sequences flanking an expression cassette containing, from 5' to 3': (a) a second region of homology containing a sequence that is homologous to a sequence in the first
• the region of homology in the first and second polynucleotides is between 50 and 500 nucleotides. In some embodiments, the region of homology in the first and second polynucleotides is between 50 and 300 nucleotides. In some embodiments, the region of homology comprises the nucleotide sequence of SEQ ID NO: 3. In some embodiments, the promoter is a chimeric CMV ⁇ actin (smcBA) promoter. In some embodiments, the promoter comprises the sequence of SEQ ID NO: 4. In some embodiments, the Otoferlin polypeptide comprises the amino acid sequence of SEQ ID NO: 5 or SEQ ID NO: 6.
• the splice donor site comprises the sequence of SEQ ID NO: 7. In some embodiments, the splice acceptor site comprises the sequence of SEQ ID NO: 8. In some embodiments, the inverted terminal repeat sequences are AAV2 inverted terminal repeat sequences. In some
• the first and second AAV particle are AAV2 serotype particles.
• the cell is ex vivo. In some embodiments, the cell is in vivo. In some
• the cell is in a mammalian subject.
• the subject has Deafness, Autosomal Recessive 9 (DFNB9).
• the disclosure provides a composition comprising a first AAV particle comprising a first polynucleotide; and a second AAV particle comprising a second
• the first polynucleotide comprises inverted terminal repeat sequences flanking an expression cassette containing, from 5' to 3' : (a) a promoter, (b) a partial coding sequence that encodes an N-terminal portion of an Otoferlin polypeptide, (c) a splice donor site, and (d) a first region of homology containing a sequence that is homologous to a sequence in the second polynucleotide, and the second polynucleotide comprises inverted terminal repeat sequences flanking an expression cassette containing, from 5' to 3': (a) a second region of homology containing a sequence that is homologous to a sequence in the first polynucleotide, (b) a splice acceptor site, (c) a partial coding sequence that encodes a C-terminal portion of the Otoferlin polypeptide, and (d) a polyadenylation (pA) signal sequence.
• pA polyadeny
• the region of homology in the first and second polynucleotides is between 50 and 500 nucleotides. In some embodiments, the region of homology in the first and second polynucleotides is between 50 and 300 nucleotides. In some embodiments, the region of homology comprises the nucleotide sequence of SEQ ID NO: 3. In some embodiments, the promoter is a chimeric CMV ⁇ actin (smcBA) promoter. In some embodiments, the promoter comprises the sequence of SEQ ID NO: 4. In some embodiments, the Otoferlin polypeptide comprises the amino acid sequence of SEQ ID NO: 5 or SEQ ID NO: 6.
• the splice donor site comprises the sequence of SEQ ID NO: 7. In some embodiments, the splice acceptor site comprises the sequence of SEQ ID NO: 8. In some embodiments, the inverted terminal repeat sequences are AAV2 inverted terminal repeat sequences. In some embodiments, the first and second AAV particle are AAV2 serotype particles. In some embodiments, the composition further comprises a pharmaceutically acceptable carrier.
• the disclosure provides a kit comprising a composition as described herein or comprising a first AAV particle as described herein and a second AAV particle as described herein.
• FIG. 1A is a map of a plasmid containing AAV2 inverted terminal repeats (TR) flanking a CMV enhancer, a chicken beta- actin promoter, a 5' section of the mouse Otoferlin cDNA (Otoferlin NT), a splice donor sequence (APSD), and a homologous sequence for recombination (APhead).
• TR inverted terminal repeats
• CMV enhancer a CMV enhancer
• chicken beta- actin promoter a 5' section of the mouse Otoferlin cDNA
• APSD a splice donor sequence
• APhead homologous sequence for recombination
• FIG. IB is a map of a plasmid containing AAV2 inverted terminal repeats (TR) flanking a homologous sequence for recombination (APhead), a splice acceptor sequence (APS A), a 3' section of the mouse Otoferlin cDNA (Otoferlin CT), a bovine growth hormone polyadenylation signal (bGH PolyA).
• TR inverted terminal repeats
• APS A splice acceptor sequence
• Otoferlin CT a 3' section of the mouse Otoferlin cDNA
• bGH PolyA bovine growth hormone polyadenylation signal
• FIG. 2 is a schematic of the two expression cassettes in the plasmids in FIGs. 1A and IB.
• FIG. 3A shows the annotated sequence of the expression cassette, including the inverted terminal repeats (TR) for the plasmid in FIG. 1A.
• TR inverted terminal repeats
• FIG. 3B shows the annotated sequence of the expression cassette, including the inverted terminal repeats (TR) for the plasmid in FIG. IB.
• FIG. 4 is a series of photographs showing expression of OTOF protein in HEK 293 cells treated with AAV2-OTOF-NT (AAV-NT) or AAV2-OTOF-NT and AAV2-OTOF-CT (AAV2- NT+CT).
• FIG. 5 is a series of photographs showing expression of GFP in the cochlea organ of Corti surface preparations from wild-type mice treated with AAV2-GFP.
• FIGs. 6A-D are a series of photographs and a graph showing OTOF expression in the cochlea of P1-P3 mice.
• FIG. 6A shows expression of OTOF protein in the mid-turn.
• FIG. 6B shows expression of OTOF protein in the apex.
• the left bar in each pair of bars is WT and the right bar in each pair of bars is Res. KO NT+CT.
• 6D shows RT-PCR data of OTOF mRNA in wild-type (WT), OTOF knock-out mice (KO) and OTOF knock-out mice treated with AAV2-OTOF-NT and AAV2-OTOF-CT (Res. KO).
• FIGs. 7A-D show a hearing assessment in mice.
• FIG. 7A is a trace of auditory brainstem response (ABR) patterns induced by auditory stimuli in wild-type mice (WT), OTOF knock-out mice either untreated (KO/KO NT) or treated (Rescued KO) with AAV2-OTOF-NT and AAV2-OTOF-CT.
• FIG. 7A is a trace of auditory brainstem response (ABR) patterns induced by auditory stimuli in wild-type mice (WT), OTOF knock-out mice either untreated (KO/KO NT) or treated (Rescued KO) with AAV2-OTOF-NT and AAV2-OTOF-CT.
• ABR auditory brainstem response
• FIG. 7B shows the auditory brainstem response (ABR) threshold in wild-type mice (WT), untreated Otoferlin knock-out mice (KO), Otoferlin knock-out mice treated with AAV2-OTOF-NT and AAV2-OTOF-CT (Res KO NT +CT), and Otoferlin knockout mice treated with AAV2-OTOF-NT (KO +NT).
• FIG. 7C shows a time course of hearing recovery in wild-type mice (WT), untreated OTOF knock-out mice (KO), Otoferlin knock-out mice treated with AAV2-OTOF-NT and AAV2-OTOF-CT (Rescued KO NT +CT), and Otoferlin knock-out mice treated with AAV2-OTOF-NT (KONT).
• FIG. 7D shows the click ABR threshold in wild-type mice (WT), untreated Otoferlin knock-out mice (KO), Otoferlin knock-out mice treated with AAV2-OTOF-NT and AAV2-OTOF-CT (Res. KO (NT +CT)), and Otoferlin knock-out mice treated with AAV2-OTOF-NT (KO +NT).
• FIGs. 8A and B show Otoferlin protein expression in the OTOF rescued KO mice inner hair cells.
• FIG. 8A shows OTOF protein expression in P12 and older mice treated with AAV2- OTOF-NT and AAV2-OTOF-CT.
• the left bar in each pair of bars is WT and the right bar in each pair of bars is Rescued KO.
• FIGs. 9A and 9B are a series of graphs showing hearing assessment.
• FIG. 9A shows
• FIG. 9B shows hearing longevity in WT, KO and Rescued KO mice.
• FIG. 10 is a map of a plasmid containing AAV2 inverted terminal repeats (TR) flanking a CMV enhancer, a chicken beta-actin promoter, a 5' section of a human Otoferlin cDNA
• FIG. 11 is a map of a plasmid containing AAV2 inverted terminal repeats (TR) flanking a homologous sequence for recombination (APhead), a splice acceptor sequence (APS A), a 3' section of a human Otoferlin cDNA (Otoferlin CT) encoding isoform 1 of Otoferlin, a bovine growth hormone polyadenylation signal (bGH PolyA).
• FIG. 12 is a map of a plasmid containing AAV2 inverted terminal repeats (TR) flanking a homologous sequence for recombination (APhead), a splice acceptor sequence (APS A), a 3' section of the mouse Otoferlin cDNA (Otoferlin CT) encoding isoform 5 of Otoferlin, a bovine growth hormone polyadenylation signal (bGH PolyA).
• FIG. 13 shows the annotated sequence of a human OTOF N-terminal expression cassette, including the inverted terminal repeats (TR) for the plasmid in FIG. 10.
• FIG. 14 shows the annotated sequence of a human OTOF C-terminal expression cassette for isoform 1, including the inverted terminal repeats (TR) for the plasmid in FIG. 11.
• FIG. 15 shows the annotated sequence of a human OTOF C-terminal expression cassette for isoform 5, including the inverted terminal repeats (TR) for the plasmid in FIG. 12.
• nucleic acid and “polynucleotide sequence” refer to a deoxyribonucleotide or ribonucleotide polymer in either single- or double- stranded form, and unless otherwise limited, encompass known analogs of natural nucleotides that can function in a similar manner as naturally occurring nucleotides.
• substantially corresponds to denote a characteristic of a nucleic acid or an amino acid sequence, wherein a selected nucleic acid or amino acid sequence has at least about 70 or about 75 percent sequence identity as compared to a selected reference nucleic acid or amino acid sequence. More typically, the selected sequence and the reference sequence will have at least about 76, 77, 78, 79, 80, 81, 82, 83, 84 or even 85 percent sequence identity, and more preferably, at least about 86, 87, 88, 89, 90, 91, 92, 93, 94, or 95 percent sequence identity. More preferably still, highly homologous sequences often share greater than at least about 96, 97, 98, or 99 percent sequence identity between the selected sequence and the reference sequence to which it was compared.
• the percentage of sequence identity may be calculated over the entire length of the sequences to be compared, or may be calculated by excluding small deletions or additions which total less than about 25 percent or so of the chosen reference sequence.
• the reference sequence may be a subset of a larger sequence, such as a portion of a gene or flanking sequence, or a repetitive portion of a chromosome.
• the reference sequence will typically comprise at least about 18-25 nucleotides, more typically at least about 26 to 35 nucleotides, and even more typically at least about 40, 50, 60, 70, 80, 90, or even 100 or so nucleotides.
• the extent of percent identity between the two sequences may be at least about 80%, preferably at least about 85%, and more preferably about 90% or 95% or higher, as readily determined by one or more of the sequence comparison algorithms well-known to those of ordinary skill in the art, such as e.g., the FASTA program analysis described by Pearson and Lipman (1988).
• polynucleotides are provided for delivering portions of coding sequences of an OTOF gene that encode the Otoferlin protein to a cell.
• the coding sequences are derived from a human OTOF gene (see, e.g., NCBI Gene ID: 9381 and cDNA sequences NM 001287489.1, NM_004802.3, NM_194248.2, NM_194322.2, and NM_194323.2).
• the coding sequences are derived from a mouse OTOF gene (see, e.g., NCBI Gene ID 83762 and cDNA sequences NM_001100395.1,
• NM_001286421.1, NM_001313767.1, and NM_031875.2 a first and a second polynucleotide are provided. It is to be understood that “first,” “second,” “third,” and the like are not meant to imply a particular order or importance unless expressly stated otherwise.
• the first polynucleotide comprises inverted terminal repeat sequences flanking an expression cassette containing, from 5' to 3', one or more of (a) a promoter, (b) a partial coding sequence that encodes an N-terminal portion of an Otoferlin polypeptide, (c) a splice donor site, and (d) a first region of homology containing a sequence that is homologous to a sequence in the second polynucleotide.
• the first polynucleotide comprises at least two, at least three or all four of (a), (b), (c), and (d).
• the second polynucleotide comprises inverted terminal repeat sequences flanking an expression cassette containing, from 5' to 3', one or more of (a) a second region of homology containing a sequence that is homologous to a sequence in the first polynucleotide, (b) a splice acceptor site, (c) a partial coding sequence that encodes a C-terminal portion of the Otoferlin polypeptide, and (d) a polyadenylation (pA) signal sequence.
• the second polynucleotide comprises at least two, at least three or all four of (a), (b), (c), and (d).
• the partial coding sequences contained within the polynucleotides described herein may be designed so that, upon delivery of the polynucleotides, the partial coding sequences are joined together, e.g., through homologous recombination, and form a complete coding sequence that encodes an Otoferlin polypeptide.
• the polynucleotides are plasmids (e.g., a circular nucleic acid comprising one or more of an origin of replication, a selectable marker, and a reporter gene).
• polynucleotides described herein, such as a plasmid may also contain marker or reporter genes, e.g., LacZ or a fluorescent protein, and an origin of replication.
• the plasmid is transfected into a producer cell that produces AAV particles containing the expression cassettes contained within the plasmids.
• the polynucleotides are nucleic acid vectors such as a
• AAV nucleic acid vectors useful according to the disclosure include single-stranded (ss) or self-complementary (sc) AAV nucleic acid vectors.
• recombinant AAV particles comprise the polynucleotides, such as a single-stranded (ss) or self-complementary (sc) AAV nucleic acid vectors.
• the polynucleotides contain expression constructs as described herein and inverted terminal repeat (ITR) sequences (e.g., wild-type ITR sequences or engineered ITR sequences) flanking the expression constructs.
• ITR inverted terminal repeat
• the polynucleotides are encapsidated by viral capsids.
• an AAV particle comprises a viral capsid and a polynucleotide as described herein, which is encapsidated by the viral capsid.
• the viral capsid comprises 60 capsid protein subunits comprising VPl, VP2 and VP3.
• the VPl, VP2, and VP3 subunits are present in the capsid at a ratio of approximately 1: 1: 10, respectively.
• polynucleotides as described herein comprise regions of homology, e.g., to promote homologous recombination between the polynucleotides once delivered to a cell (see, e.g., Ghosh et al. Efficient transgene reconstitution with hybrid dual AAV vectors carrying the minimized bridging sequences. Hum Gene Ther. 2011 Jan;22(l):77-83).
• a first region of homology and a second region of homology have a threshold level of sequence identity with each other in order to promote homologous recombination.
• the first region of homology has at least 75%, at least 80%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or 100% identity with the second region of homology.
• Gapped BLAST can be used as described (Altschul et al., 1997).
• the default parameters of the respective programs (NBLAST and XBLAST) can be used in accordance with published methods.
• each region of homology is independently between 50 and 500, 50 and 400, 50 and 300, 100 and 500, 100 and 400, 100 and 300, 200 and 500, 200 and 400, or 200 and 300 nucleotides.
• the regions of homology are identical and each region of homology is between 50 and 500, 50 and 400, 50 and 300, 100 and 500, 100 and 400, 100 and 300, 200 and 500, 200 and 400, or 200 and 300 nucleotides.
• the region homology comprises a sequence that is at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or 100% identical with the nucleotide sequence
• polynucleotides described herein may comprise one or more regulatory elements.
• a person of ordinary skill in the art can select regulatory elements for use in appropriate host cells, for example, mammalian or human host cells. Regulatory elements include, for example, promoters, transcription termination sequences, translation termination sequences, enhancers, and polyadenylation elements.
• a polynucleotide described herein may comprise a promoter sequence operably linked to a nucleotide sequence encoding a desired polypeptide, such as Otoferlin.
• Promoters contemplated for use in the subject invention include, but are not limited to, cytomegalovirus (CMV) promoter, SV40 promoter, Rous sarcoma virus (RSV) promoter, chimeric CMV/chicken ⁇ actin promoter (CBA) and the truncated form of CBA (smCBA) (see, e.g., Haire et al. 2006 and U.S. Patent No. 8,298,818, which is specifically incorporated herein in its entirety by express reference thereto).
• the promoter is the truncated chimeric CMV ⁇ actin (smcBA) promoter.
• the promoter comprises a sequence that is at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or 100% identical with the nucleotide sequence
• polynucleotides as described herein comprise a partial coding sequence that encodes an N-terminal or C-terminal portion of an Otoferlin polypeptide, wherein the partial coding sequences can be spliced or otherwise combined together in vivo in order to encode an Otoferlin polypeptide.
• the Otoferlin polypeptide is a human Otoferlin polypeptide.
• the Otoferlin polypeptide is a long isoform of a human Otoferlin polypeptide (see, e.g., Yasunaga et al.
• the Otoferlin polypeptide comprises a sequence that is at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or 100% identical with one or both of the following amino acid sequences:
• the Otoferlin polypeptide is a mouse Otoferlin polypeptide. In some embodiments, the Otoferlin polypeptide comprises a sequence that is at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or 100% identical with the following amino acid sequence:
• the splice donor and/or splice acceptor sites contain splice consensus sequences. In some embodiments, the splice donor and/or splice acceptor sites contain sequences splice consensus sequences derived from alkaline phosphatase. In some embodiments, the splice donor site comprises a sequence that is at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or 100% identical with the nucleotide sequence
• the splice acceptor site comprises a sequence that is at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or 100% identical with the nucleotide sequence
• polynucleotides described herein comprise ITR sequences.
• the ITR sequences of a polynucleotide described herein can be derived from any AAV serotype (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10) or can be derived from more than one serotype.
• the ITR sequences are derived from AAV2.
• ITR sequences and plasmids containing ITR sequences are known in the art and commercially available (see, e.g., products and services available from Vector Biolabs, Philadelphia, PA;
• Kessler PD Podsakoff GM, Chen X, McQuiston SA, Colosi PC, Matelis LA, Kurtzman GJ, Byrne BJ. Proc Natl Acad Sci U S A. 1996 Nov 26;93(24): 14082-7; and Curtis A. Machida. Methods in Molecular MedicineTM. Viral Vectors for Gene Therapy Methods and Protocols. 10.1385/1-59259-304-6:201 ⁇ Humana Press Inc. 2003. Chapter 10. Targeted Integration by Adeno-Associated Virus.
• An exemplary AAV2 ITR sequence for flanking the 5' end of an expression construct comprises the sequence:
• An exemplary AAV2 ITR sequence for flanking the 3' end of an expression construct comprises the sequence
• polynucleotides described herein may further optionally include one or more transcription termination sequences, one or more translation termination sequences, one or more signal peptide sequences, one or more internal ribosome entry sites (IRES), and/or one or more enhancer elements, or any combination thereof.
• Transcription termination regions can typically be obtained from the 3' untranslated region of a eukaryotic or viral gene sequence. Transcription termination sequences can be positioned downstream of a coding sequence to provide for efficient termination.
• Signal peptide sequences are amino-terminal peptidic sequences that encode information responsible for the location of an operably-linked polypeptide to one or more post-translational cellular destinations, including, for example, specific organelle compartments, or to the sites of protein synthesis and/or activity, and even to the extracellular environment.
• a polynucleotide as described herein comprises a bovine growth hormone polyadenylation signal.
• the expression constructs contained within the polynucleotides described herein are no more than 5 kilobases, no more than 4 kilobases, or no more than 3 kilobases in size. In some embodiments, the expression construct is between 4 and 5 kilobases in size.
• polynucleotides described herein are contained within one or more recombinant AAV particles (e.g., first and second AAV particles).
• the AAV particles may be of any AAV serotype (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10), including any derivative
• Non-limiting examples of derivatives and pseudotypes include AAV2-AAV3 hybrid, AAVrh. lO, AAVhu.14,
• the first and second AAV particle are AAV2 serotype particles.
• AAV particles and polynucleotides are known in the art and commercially available (see, e.g., Zolotukhin et al. Production and purification of serotype 1, 2, and 5 recombinant adeno-associated viral vectors. Methods 28 (2002) 158-167; and U.S. Patent Publication Numbers US20070015238 and US20120322861, which are incorporated herein by reference; and plasmids and kits available from ATCC and Cell Biolabs, Inc.).
• the polynucleotides may be combined with one or more helper plasmids, e.g., that contain a rep gene (e.g., encoding Rep78, Rep68, Rep52 and Rep40) and a cap gene (encoding VPl, VP2, and VP3), and transfected into a producer cell line such that the AAV particle can be packaged and subsequently purified.
• helper plasmids e.g., that contain a rep gene (e.g., encoding Rep78, Rep68, Rep52 and Rep40) and a cap gene (encoding VPl, VP2, and VP3)
• the one or more helper plasmids includes a first helper plasmid comprising a rep gene and a cap gene and a second helper plasmid comprising other genes that assist in AAV production, such as a Ela gene, a Elb gene, a E4 gene, a E2a gene, and a VA gene.
• the rep gene is a rep gene derived from AAV2.
• Helper plasmids, and methods of making such plasmids are known in the art and commercially available (see, e.g., pDM, pDG, pDPlrs, pDP2rs, pDP3rs, pDP4rs, pDP5rs, pDP6rs, pDG(R484E/R585E), and pDP8.ape plasmids from PlasmidFactory, Bielefeld, Germany; other products and services available from Vector Biolabs, Philadelphia, PA; Cellbiolabs, San Diego, CA; Agilent
• helper plasmids are produced or obtained, which comprise rep and cap ORFs for the desired AAV serotype and the adenoviral VA, E2A (DBP), and E4 genes under the
• HEK293 cells are transfected via CaP0 4 -mediated transfection, lipids or polymeric molecules such as
• PEI Polyethylenimine
• Sf9-based producer stable cell lines are infected with a single recombinant baculovirus containing the polynucleotide.
• HEK293 or BHK cell lines are infected with a HSV containing the polynucleotide and optionally one or more helper HSVs containing rep and cap ORFs as described herein and the adenoviral VA, E2A (DBP), and E4 genes under the transcriptional control of their native promoters.
• the HEK293, BHK, or Sf9 cells are then incubated for at least 60 hours to allow for AAV particle production.
• the AAV particles can then be purified using any method known in the art or described herein, e.g., by iodixanol step gradient, CsCl gradient, chromatography, or polyethylene glycol (PEG) precipitation.
• the disclosure also contemplates host cells that comprise at least one of the disclosed AAV particles or polynucleotides.
• host cells include mammalian host cells, with human host cells being preferred, and may be either isolated, in cell or tissue culture.
• the transformed host cells may be comprised within the body of a non-human animal itself.
• the method comprises contacting the cell with a first AAV particle as described herein comprising a first polynucleotide as described herein; and contacting the cell with a second AAV particle as described herein comprising a second polynucleotide as described herein.
• the cell is a mammalian cell such as a mouse or human cell.
• the cell is ex vivo.
• the cell is in vivo.
• the cell is a cell of the ear (e.g., the cell of a human ear).
• the cell is a cell of the inner ear (e.g., the cell of a human inner ear). In some embodiments, the cell is in a subject (e.g., a mammalian subject such as a human subject).
• a subject e.g., a mammalian subject such as a human subject.
• the method comprises administering to a subject a therapeutically effective amount of a first AAV particle as described herein comprising a first polynucleotide as described herein and a therapeutically effective amount of a second AAV particle as described herein comprising a second
• the subject is a human subject and the subject has Deafness, Autosomal Recessive 9 (DFNB9).
• DFNB9 Deafness, Autosomal Recessive 9
• the subject is a human subject having impaired vestibular function or a vestibular disorder (see, e.g., Dulon et al. Otoferlin is Critical for a Highly Sensitive and Linear Calcium Dependent Exocytosis at Vestibular Hair Cell Ribbon Synapses. J Neurosci. 2009; 29(34): 10474-10487).
• compositions described above or elsewhere herein are typically administered to a subject in an effective amount, that is, an amount capable of producing a desirable result.
• the desirable result will depend upon the active agent being administered.
• an effective amount of AAV particles may be an amount of the particles that are capable of transferring an expression construct to a host organ, tissue, or cell.
• a therapeutically acceptable amount may be an amount that is capable of treating a disease, e.g., DFNB9.
• dosage for any one subject depends on many factors, including the subject's size, body surface area, age, the particular composition to be administered, the active ingredient(s) in the composition, time and route of administration, general health, and other drugs being administered concurrently.
• the AAV particles or polynucleotides may be delivered in the form of a composition, such as a composition comprising the active ingredient, such as AAV particles described herein, and a pharmaceutically acceptable carrier as described herein.
• the AAV particles or polynucleotides may be prepared in a variety of compositions, and may also be formulated in appropriate pharmaceutical vehicles for administration to human or animal subjects.
• first and second AAV particles may be utilized, the first and second AAV particles may be contained within the same composition or within different compositions and may be administered together or separately.
• the AAV particles administered to a subject may be provided in a composition having a concentration on the order ranging from 10 6 to 10 14 particles/ml or 10 3 to 10 15 particles/ml, or any values there between for either range, such as for example, about 10 6 , 10 7 , 10 8 , 10 9 , 10 10 , 10 11 , 10 12 , 10 13 , or 10 14 particles/ml. In one embodiment, AAV particles of higher than 10 13 particles/ml are be administered.
• the number of AAV particles administered to a subject may be on the order ranging from 10 6 to 10 14 vector genomes(vgs)/ml or 10 3 to 1015 vgs/ml, or any values therebetween for either range, such as for example, about 10 6 , 10 7 , 10 8 , 10 9 , 10 10 , 10 11 , 10 12 , 10 13 , or 10 14 vgs/ml. In one embodiment,
• AAV particles of higher than 10 13 vgs/ml are be administered.
• the AAV particles can be administered as a single dose, or divided into two or more administrations as may be required to achieve therapy of the particular disease or disorder being treated.
• 0.0001 ml to 10 mis are delivered to a subject.
• the number of AAV particles administered to a subject may be on the order ranging from 10 6 -10 14 vg/kg, or any values therebetween, such as for example, about 10 6 , 10 7 , 10 8 , 10 9 , 10 10 , 10 11 , 10 12 , 10 13 , or 10 14 vgs/kg.
• the amount administered is the same for both particles. In some embodiments, when a first AAV particle comprising a first polynucleotide as described herein and second AAV particle comprising a second polynucleotide as described herein are administered, the amount administered is different for each particle.
• AAV particles may be administered in combination with other agents or treatments as well, such as, e.g., proteins or polypeptides or various pharmaceutic ally- active agents, including one or more systemic or topical administrations of therapeutic polypeptides, biologically active fragments, or variants thereof.
• agents or treatments such as, e.g., proteins or polypeptides or various pharmaceutic ally- active agents, including one or more systemic or topical administrations of therapeutic polypeptides, biologically active fragments, or variants thereof.
• agents or treatments such as, e.g., proteins or polypeptides or various pharmaceutic ally- active agents, including one or more systemic or topical administrations of therapeutic polypeptides, biologically active fragments, or variants thereof.
• the additional agents do not cause a significant adverse effect upon contact with the target cells or host tissues.
• the AAV particles may thus be delivered along with various other agents or treatments as required in the particular instance.
• AAV particle treatment may be accompanied by use of
• the administration is a route suitable for systemic delivery, such as by intravenous injection or infusion.
• the administration is to the ear, e.g., via intra-cochlear administration.
• the pharmaceutical forms of the AAV particle compositions suitable for injectable use include sterile aqueous solutions or dispersions.
• the form is sterile and fluid to the extent that easy syringability exists.
• the form is stable under the conditions of manufacture and storage and is preserved against the contaminating action of microorganisms, such as bacteria and fungi.
• the carrier can be a solvent or dispersion medium containing, for example, water, saline, ethanol, polyol (e.g., glycerol, propylene glycol, and liquid polyethylene glycol, and the like), suitable mixtures thereof, and/or vegetable oils.
• polyol e.g., glycerol, propylene glycol, and liquid polyethylene glycol, and the like
• suitable mixtures thereof e.g., glycerol, propylene glycol, and liquid polyethylene glycol, and the like
• vegetable oils e.g., glycerol, propylene glycol, and liquid polyethylene glycol, and the like
• Proper fluidity may be maintained, for example, by the use of a coating, such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use
• the solution may be suitably buffered, if necessary, and the liquid diluent first rendered isotonic with sufficient saline or glucose.
• aqueous solutions are especially suitable for intravenous, intramuscular, intravitreal, subretinal, subcutaneous and intraperitoneal administration.
• a sterile aqueous medium that can be employed will be known to those of skill in the art in light of the present disclosure.
• one dosage may be dissolved in 1 ml of isotonic NaCl solution and either added to 1000 ml of hypodermoclysis fluid or injected at the proposed site of infusion, (see for example, "Remington's Pharmaceutical Sciences” 15th Edition, pages 1035-1038 and 1570-1580). Some variation in dosage will necessarily occur depending on the condition of the subject being treated. The person responsible for
• administration will, in any event, determine the appropriate dose for the individual subject. Moreover, for human administration, preparations should meet sterility, pyrogenicity, and the general safety and purity standards as required by, e.g., FDA Office of Biologies standards.
• Sterile injectable solutions are prepared by incorporating the AAV particles in the required amount in the appropriate solvent with several of the other ingredients enumerated above, as required, followed by filtered sterilization or another sterilization technique.
• dispersions are prepared by incorporating the various sterilized active ingredients into a sterile vehicle which contains the basic dispersion medium and the required other ingredients from those enumerated above.
• a sterile vehicle which contains the basic dispersion medium and the required other ingredients from those enumerated above.
• the preferred methods of preparation are vacuum-drying and freeze-drying techniques which yield a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.
• AAV particle or polynucleotide compositions and time of administration of such compositions will be within the purview of the skilled artisan having benefit of the present teachings. It is likely, however, that the administration of therapeutically effective amounts of the disclosed compositions may be achieved by a single administration, such as for example, a single injection of sufficient numbers of infectious particles to provide therapeutic benefit to the patient undergoing such treatment. Alternatively, in some circumstances, it may be desirable to provide multiple, or successive administrations of the AAV particle
• compositions either over a relatively short, or a relatively prolonged period of time, as may be determined by the medical practitioner overseeing the administration of such compositions.
• composition may include AAV particles, either alone, or in combination with one or more additional active ingredients, which may be obtained from natural or recombinant sources or chemically synthesized.
• Toxicity and efficacy of the compositions utilized in methods of the disclosure can be determined by standard pharmaceutical procedures, using either cells in culture or experimental animals to determine the LD50 (the dose lethal to 50% of the population).
• the dose ratio between toxicity and efficacy is the therapeutic index and it can be expressed as the ratio LD50/ED50.
• Those compositions that exhibit large therapeutic indices are preferred. While those that exhibit toxic side effects may be used, care should be taken to design a delivery system that minimizes the potential damage of such side effects.
• the dosage of compositions as described herein lies generally within a range that includes an ED50 with little or no toxicity. The dosage may vary within this range depending upon the dosage form employed and the route of administration utilized.
• Non-limiting examples of non-human primate subjects include macaques (e.g., cynomolgus or rhesus macaques), marmosets, tamarins, spider monkeys, owl monkeys, vervet monkeys, squirrel monkeys, baboons, gorillas, chimpanzees, and orangutans.
• the subject is a human subject.
• Other exemplary subjects include domesticated animals such as dogs and cats; livestock such as horses, cattle, pigs, sheep, goats, and chickens; and other animals such as mice, rats, guinea pigs, and hamsters.
• the subject has or is suspected of having a disease that may be treated with gene therapy.
• the subject has or is suspected of having Deafness, Autosomal Recessive 9 (DFNB9).
• DFNB9 is an autosomal recessive form of deafness though to be caused by mutations in the OTOF gene that result in a decrease in expression, functionality, or both, of the Otoferlin protein.
• Otoferlin protein has been shown to be important for exocytosis at the auditory ribbon synapse (see, e.g., Roux et al.
• Otoferlin, defective in a human deafness form is essential for exocytosis at the auditory ribbon synapse.
• Subjects having DFNB9 can be identified by the skilled physician, e.g., using a combination of electrophysiologic testing of auditory brain stem responses (ABRs) and genetic testing to identify mutations in the OTOF gene (see, e.g., OMIM entries 603681 and 601071).
• the subject is a human subject that has one or more of the following nonsense or missense mutations in the OTOF gene: TYR730TER, GLN829TER, PR01825ALA, PRO50ARG, LEU1011PRO, ILE515THR, ARG1939GLN,or GLY541SER.
• the subject is a human subject that has an A-to-G transition at the intron 8/exon 9 junction (IVS8-2A-G) or an G-to-A transition at position +1, the first intronic nucleotide in the splice donor site of exon 5 or a G-C transversion in the donor splice site of intron 39.
• the subject is a human subject that has a one base pair deletion (1778G) in exon 16, leading to a stop codon, and a 6141G-A change, resulting in an ARG-to- GLN substitution in exon 48.
• Compositions Other aspects of the disclosure relate to compositions comprising AAV particles or polynucleotides described herein.
• AAV particles described herein are added to a composition, e.g., a pharmaceutical composition.
• the composition comprises a pharmaceutically acceptable carrier.
• carrier refers to a diluent, adjuvant, excipient, or vehicle with which the AAV particles are administered.
• Such pharmaceutical carriers can be sterile liquids, such as water and oils, including those of petroleum oil such as mineral oil, vegetable oil such as peanut oil, soybean oil, and sesame oil, animal oil, or oil of synthetic origin. Saline solutions and aqueous dextrose and glycerol solutions can also be employed as liquid carriers.
• Non-limiting examples of pharmaceutically acceptable carriers include lactose, dextrose, sucrose, sorbitol, mannitol, starches, gum acacia, calcium phosphate, alginates, tragacanth, gelatin, calcium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, water, saline, syrup, methylcellulose, ethylcellulose, hydroxypropylmethylcellulose, polyacrylic acids, lubricating agents (such as talc, magnesium stearate, and mineral oil), wetting agents, emulsifying agents, suspending agents, preserving agents (such as methyl-, ethyl-, and propyl-hydroxy-benzoates), and pH adjusting agents (such as inorganic and organic acids and bases).
• lactose dextrose, sucrose, sorbitol, mannitol, starches, gum acacia, calcium phosphate, alginates, tragacanth, gelatin, calcium si
• carriers include phosphate buffered saline, HEPES -buffered saline, and water for injection, any of which may be optionally combined with one or more of calcium chloride dihydrate, disodium phosphate anhydrous, magnesium chloride hexahydrate, potassium chloride, potassium dihydrogen phosphate, sodium chloride, or sucrose.
• carriers that might be used include saline (e.g., sterilized, pyrogen-free saline), saline buffers (e.g., citrate buffer, phosphate buffer, acetate buffer, and bicarbonate buffer), amino acids, urea, alcohols, ascorbic acid, phospholipids, proteins (for example, serum albumin), EDTA, sodium chloride, liposomes, mannitol, sorbitol, and glycerol. USP grade carriers and excipients are particularly useful for delivery of AAV particles to human subjects.
• saline e.g., sterilized, pyrogen-free saline
• saline buffers e.g., citrate buffer, phosphate buffer, acetate buffer, and bicarbonate buffer
• amino acids e.g., citrate buffer, phosphate buffer, acetate buffer, and bicarbonate buffer
• amino acids e.g., citrate buffer, phosphate buffer, acetate
• compositions may further optionally comprise a liposome, a lipid, a lipid complex, a microsphere, a microparticle, a nanosphere, or a nanoparticle, or may be otherwise formulated for administration to the cells, tissues, organs, or body of a subject in need thereof.
• Methods for making such compositions are well known and can be found in, for example, Remington: The Science and Practice of Pharmacy, 22 nd edition, Pharmaceutical Press, 2012.
• compositions may contain at least about 0.1% of the therapeutic agent (e.g., AAV particles) or more, although the percentage of the active ingredient(s) may, of course, be varied and may conveniently be between about 1 or 2% and about 70% or 80% or more of the weight or volume of the total formulation.
• the amount of therapeutic agent(s) (e.g., AAV particles) in each therapeutically-useful composition may be prepared in such a way that a suitable dosage will be obtained in any given unit dose of the compound.
• a composition described herein may be administered to a subject in need thereof, such as a subject having DFNB9.
• a method described herein may comprise administering a composition or multiple compositions comprising AAV particles as described herein to a subject in need thereof.
• the subject is a human subject.
• the subject has or is suspected of having a disease that may be treated with gene therapy, such as DFNB9.
• the subject has been diagnosed with DFNB9.
• kits comprising AAV particles or
• Kits can optionally include pharmaceutically acceptable carriers and/or diluents.
• the kit includes instructions or packaging materials that describe how to administer AAV particles or polynucleotides contained within the kit to a selected cell or recipient.
• Containers of the kit can be of any suitable material, e.g., glass, plastic, metal, etc., and of any suitable size, shape, or configuration.
• the kits may include one or more ampoules or syringes that contain AAV particles or polynucleotides in a suitable liquid or solution form.
• Otoferlin is the key calcium sensor for neurotransmitter release in the ear (see, e.g., Roux 2006). Otoferlin is mainly expressed in the inner hair cells of the cochlea and only few other cells of the central nervous system (see, e.g., Yasunaga et al. 1999& 2000). It is a member of the ferlin family of transmembrane proteins which share a common C2 domain also found in synaptotagmin, PKC and PLC.
• OTOF knock-out mice have also been shown to have severe hearing loss despite normal inner hair cell development and auditory ribbon synapse formation (see, e.g., Roux et al. (2006) Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse. Cell. 127:277-289).
• Otof /_ mice lose the auditory brain stem response across all sound frequencies due to complete abolishment of synaptic exocytosis and, as a consequence, abolishment of neurotransmitter release from synaptic vesicles.
• DFNB9 manifests in humans as two phenotypes, as a nonsyndromic bilateral loss of hearing before the acquiring of language and less frequently as a temperature-sensitive nonsyndromic auditory neuropathy. It was first discovered in an affected Lebanese family (Chaib et al. 1996) and has since been found in many parts of the world (see, e.g., Adato et al. 2000, Rodriguez-Ballesteros et al. 2003, Choi et al. 2009, Matsunaga et al. 2012).
• adeno-associated virus AAV
• AAV adeno-associated virus
• the mouse OTOF cDNA is 5979 base pairs in length whereas most AAVs cannot package more than approximately 4.8 kilobases of genome.
• a dual vector system was used to separately deliver the 5' portion of the cDNA and the 3' portion of the cDNA as separate AAV constructs such that the full-length cDNA could be reassembled in vivo once delivered.
• a mouse OTOF cDNA was split into two sections, a 5' and 3' section and inserted into two AAV ITR-containing plasmids.
• the sequence of each of the two cassettes in the plasmids is shown below and the maps of each construct are shown in FIGs. 1 and 2.
• Annotated versions of the cassettes are shown in FIGs. 3 A and 3B.
• Each cassette contains a region of homology to promote homologous recombination between the 5' and 3' ends of the cDNA in vivo (see Ghosh et al., 2011). Once recombined in vivo, the full-length cDNA contains a splice donor/splice acceptor pair that causes splicing out of the region of homology.
• the vectors were packaged into AAV2 serotype particles using standard plasmid transfection methods as previously described (see Zolotukhin et al. Production and purification of serotype 1, 2, and 5 recombinant adeno-associated viral vectors. Methods 28 (2002) 158-167).
• the viral particles were purified by standard methods as previously described (see Zolotukhin et al. Production and purification of serotype 1, 2, and 5 recombinant adeno-associated viral vectors. Methods 28 (2002) 158— 167).
• the viral particles carrying the 5' portion of the OTOF cDNA are also referred to herein as "AAV2-OTOF-NT.”
• the viral particles carrying the 3' portion of the OTOF cDNA are also referred to herein as "AAV2-OTOF-CT.”
• HEK 293 cells were grown on poly-lysine-coated coverslips in growth medium. ⁇ of each virus was used for each well as follows: Control cells without virus, cells with AAV2- OTOF n-terminal portion (AAV2-OTOF-NT), cells with AAV2-OTOF c-terminal portion (AAV2-OTOF-CT) and cells with both viruses (AAV2-OTOF-NT and A A V2-OTOF-CT) . The cells were stained with anti-OTOF antibody and mounted on glass slides. OTOF knock-out mice
• the OTOF knock-out mice used were generated in a previous study (see Roux et al. (2006) Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse. Cell. 127:277-289). Briefly, two fragments containing the genomic sequences 5' and 3' to exons 14 and 15 of Otof were amplified by PCR.
• the 5 kb BamHI-XhoI-BssHII and 6 kb BssHII-Sfil-BamHI-Nael 129/SvPas fragments were inserted into pUC19 (New England BioLabs) previously modified by inserting a BamHI-XhoI-BssHII-Sfil-Nael-Hindlll polylinker.
• a loxP-hygro-loxP (the gene conferring resistance to hygromycin under control of the phosphoglycerate kinase gene [Pgk-1] promoter) cassette was inserted into the BssHII site.
• F2 animals carrying an allele in which the hygromycin selection cassette was deleted were selected by PCR, using primers 5' -CACTTGCTTTGTCT CATCTCC-3' (SEQ ID NO: 12) and 5' - GTC ACTTCTTCTGGGTATTTC-3 ' (SEQ ID NO: 13), generating a 507 base pair PCR product.
• the heterozygous animals were interbred to generate Otof 7" , Otof +/ ⁇ , and Otof +/+ mice.
• the knockout mice were generated in C57BL/6-129/SvPas background as described above. Because this background strain is known to have some age-related hearing loss, the mice were backcrossed with FVB mice strain to the 10 th generation to obtain an FVB homogeneous genetic background with no known age-related hearing loss.
• AAV2-OTOF-NT (6.32xl0 12 vg/ml) and AAV2-OTOF-CT (4.5xl0 12 vg/ml) were delivered through the RWM to Pl-3 mice.
• AAV2- OTOF-NT (1.43xl0 13 vg/ml) and AAV2-OTOF-CT (3.12xl0 13 vg/ml) were delivered through the RWM to P>12 mice.
• ABR tests were conducted 7 days after injection. Expression of OTOF protein in the mice was measured using anti-OTOF antibody to label cells in cochlear whole mounts. Reverse-transcriptase (RT)-PCR was used to screen for the presence of OTOF mRNA within the cochlear tissue of the mice. Wild-type mice were also injected using the same technique with AAV2-GFP to assess viral delivery to cochlea with AAV2 serotype. Cochlea were whole mounted and stained with anti-GFP antibody.
• mice were anesthetized by intraperitoneal injection of a mixture of ketamine hydrochloride (Ketaset, 100 mg/ml) and xylazine hydrochloride (xyla-ject, 10 mg/ml) and boosted with one-fifth the original dose as required. Body temperature was maintained with a heating pad and monitored with a rectal probe throughout recording.
• the evoked acoustic brainstem response (ABR) thresholds were differentially recorded from the scalp of the mice. Responses were recorded using subdermal needle electrodes at the vertex, below the pinna of the left ear (reference), and below the contralateral ear (ground).
• the sound stimuli used included clicks (5 ms duration, 31 Hz) and tone pips at 8, 16, and 32 kHz (10 ms duration, cos2 shaping, 21 Hz). Measurements were recorded using the TDT BioSig III system (Tucker Davis Technologies). For each stimulus, electroencephalographic (EEG) activity was recorded for 20 ms (at a sampling rate of 25 kHz) and filtered (0.3-3 kHz). Waveforms from 512 stimuli were averaged for click responses.
• Waveforms from 1000 stimuli were examined to identify frequency-specific tone -burst stimuli (8, 16, and 32 kHz).
• ABR waveforms were recorded in 5 dB sound pressure level (SPL) intervals down from the maximum amplitude.
• SPL sound pressure level
• the threshold was defined as the lowest stimulus level at which response peaks for waves I-V were clearly and repetitively present upon visual inspection. These threshold judgments were confirmed by analysis of stored waveforms. The comparison of each group of animals was performed using one way ANOVA with Bonferroni's post hoc testing.
• AAV plasmid constructs Two different AAV plasmid constructs were generated to deliver the 5' half and the 3' half of the mouse OTOF cDNA to the inner ear of OTOF knock-out mice (OTOF N-terminal virus and OTOF C-terminal virus). The two constructs were packaged separately into AAV2 particles. The AAV2 particles were then pooled together and used to treat HEK 293 cells or were injected into the inner ear of OTOF knock-out mice.
• HEK 293 cells only expressed Otoferlin protein when transfected with both viruses (FIG. 4). No expression of Otoferlin protein was observed in untreated cells, or in cells transfected with only the OTOF N-terminal (FIG. 4) or OTOF C-terminal virus.
• AAV2 transduces the mouse cochlea effectively.
• mice were then treated with the pooled OTOF N-terminal and C-terminal viruses and compared to various controls. Otoferlin protein was found to be expressed upon treatment with both viruses (FIG. 6). The largest number of transfected inner hair cells (IHCs) were observed in the base and fewer in the mid-turn and apex (FIG. 6). IHCs counts demonstrated that -11% of IHCs were labeled overall, with significant differences seen between the base (-29%), mid-turn (-8%), and apex (-2%). (FIG. 6). RT-PCR was used to show that OTOF mRNA was in whole cochlear extract and was the same size in both wild-type and OTOF knock-out mice treated with both viruses (FIG. 6). In contrast, the untreated OTOF knock-out mouse cochleae did not demonstrate OTOF mRNA expression. No products were detected when RT-PCR was performed in the absence of reverse transcriptase.
• Example 2 Human OTOF dual vector constructs Provided below are example dual vector sequences for expressing Human Otoferlin protein isoforms 1 and 5.
• the cDNAs encoding both isoforms 1 and 5 contain the same N- terminal sequence such that the same N-terminal vector can be used for expressing both isoforms.
• Vector maps and annotated sequences corresponding to the below sequences are shown in FIGs. 10-15.
• Roux I Roux I, Safieddine S, Nouvian R, Grati M, Simmler MC, Bahloul A, Perfettini I, Le Gall M, Rostaing P, Hamard G, Triller A, Avan P, Moser T, Petit C. Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse. Cell. 2006 Oct 20;127(2):277-89. 2) Wu Z, Yang H, Colosi P. Effect of genome size on AAV vector packaging. Mol Ther.
• inventive embodiments are presented by way of example only and that, within the scope of the appended claims and equivalents thereto, inventive embodiments may be practiced otherwise than as specifically described and claimed.
• inventive embodiments of the present disclosure are directed to each individual feature, system, article, material, kit, and/or method described herein.
• a reference to "A and/or B", when used in conjunction with open-ended language such as “comprising” can refer, in one embodiment, to A only (optionally including elements other than B); in another embodiment, to B only (optionally including elements other than A); in yet another embodiment, to both A and B (optionally including other elements); etc.
• the phrase "at least one,” in reference to a list of one or more elements, should be understood to mean at least one element selected from any one or more of the elements in the list of elements, but not necessarily including at least one of each and every element specifically listed within the list of elements and not excluding any combinations of elements in the list of elements.
• This definition also allows that elements may optionally be present other than the elements specifically identified within the list of elements to which the phrase "at least one" refers, whether related or unrelated to those elements specifically identified.
• At least one of A and B can refer, in one embodiment, to at least one, optionally including more than one, A, with no B present (and optionally including elements other than B); in another embodiment, to at least one, optionally including more than one, B, with no A present (and optionally including elements other than A); in yet another embodiment, to at least one, optionally including more than one, A, and at least one, optionally including more than one, B (and optionally including other elements); etc.

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