Compositions and methods for treating non-age-associated hearing impairment in a human subject
Provided herein are compositions that include at least two different nucleic acid vectors, where each of the at least two different vectors includes a coding sequence that encodes a different portion of an otoferlin protein, and the use of these compositions to treat hearing loss in a subject.
1. A composition comprising two different nucleic acid vectors, wherein:
each of the two different vectors comprises a coding sequence that encodes a different portion of an otoferlin protein, each of the encoded portions being at least 30 amino acid residues in length;
no single vector of the at least two different vectors encodes a full-length otoferlin protein;
a first of the two different vectors comprises a promoter operably linked to a coding sequence that encodes an N-terminal portion of the otoferlin protein;
at least one of the coding sequences comprises a nucleotide sequence spanning two neighboring exons of otoferlin genomic DNA, and lacks an intronic sequence between the two neighboring exons; and
when introduced into a mammalian cell the at least two different vectors undergo concatamerization or homologous recombination with each other, thereby forming a recombined nucleic acid that encodes a full-length otoferlin protein.
2. The composition of claim 1 , wherein each of the two different vectors is a viral vector selected from an adeno-associated virus (AAV) vector, an adenovirus vector, a lentivirus vector, or a retrovirus vector.
3. The composition of claim 1 , wherein each of the two different vectors is an AAV vector.
4. The composition of claim 1 , wherein the N-terminal portion of the otoferlin protein is between 30 amino acids to 1600 amino acids in length.
5. The composition of claim 1 , wherein the first vector further comprises a Kozak sequence.
6. The composition of claim 1 , wherein the promoter is an inducible promoter.
7. The composition of claim 1 , wherein a second of the two different vectors comprises a coding sequence that encodes a C-terminal portion of the otoferlin protein, and wherein the C-terminal portion of the otoferlin protein is between 30 amino acids to 1600 amino acids in length.
8. The composition of claim 7 , wherein the second vector further comprises a poly (pA) sequence.
9. The composition of claim 1 , further comprising a pharmaceutically acceptable excipient.
10. A kit comprising a vial comprising the composition of claim 1 .
11. A kit comprising a pre-loaded syringe comprising the composition of claim 1 .
12. The composition of claim 1 , wherein the promoter is a constitutive promoter.
13. The composition of claim 1 , wherein the promoter is a tissue-specific promoter.
14. The composition of claim 1 , wherein the otoferlin protein is an otoferlin isoform 5 protein.
15. The composition of claim 1 , wherein each of the two different vectors are encapsulated by AAV capsids and wherein the AAV capsids are AAV serotype 1, 2, 3, 4, 5, 6, 7, 8, 9, rh8, rh10, rh39, rh43, or Anc80.
16. A composition comprising two different nucleic acid vectors, wherein:
a first nucleic acid vector of the two different nucleic acid vectors comprises a promoter, a first coding sequence that encodes an N-terminal portion of an otoferlin protein positioned 3′ of the promoter, and a splicing donor signal sequence positioned at the 3′ end of the first coding sequence; and
a second nucleic acid vector of the two different nucleic acid vectors comprises a splicing acceptor signal sequence, a second coding sequence that encodes a C-terminal portion of an otoferlin protein positioned at the 3′ end of the splicing acceptor signal sequence, and a polyadenylation sequence at the 3′ end of the second coding sequence;
wherein each of the encoded portions is at least 30 amino acid residues in length,
wherein the amino acid sequences of the encoded portions do not overlap,
wherein no single vector of the two different vectors encodes a full-length otoferlin protein, and,
when the coding sequences are transcribed in a mammalian cell, to produce RNA transcripts, splicing occurs between the splicing donor signal sequence on one transcript and the splicing acceptor signal sequence on the other transcript, thereby forming a recombined RNA molecule that encodes a full-length otoferlin protein.
17. A kit comprising a vial comprising the composition of claim 16 .
18. A kit comprising a pre-loaded syringe comprising the composition of claim 16 .
19. The composition of claim 16 , wherein each of the two different vectors is a viral vector selected from an adeno-associated virus (AAV) vector, an adenovirus vector, a lentivirus vector, or a retrovirus vector.
20. The composition of claim 16 , wherein each of the at least two different vectors is an AAV vector.
21. The composition of claim 16 , wherein each of the two different vectors are encapsulated by AAV capsids and wherein the AAV capsids are AAV serotype 1, 2, 3, 4, 5, 6, 7, 8, 9, rh8, rh10, rh39, rh43, or Anc80.
22. The composition of claim 16 , wherein the N-terminal portion of the otoferlin protein is between 30 amino acids to 1600 amino acids in length.
23. The composition of claim 16 , wherein the first vector further comprises a Kozak sequence.
24. The composition of claim 16 , wherein the promoter is an inducible promoter.
25. The composition of claim 16 , wherein the promoter is a constitutive promoter.
26. The composition of claim 16 , wherein the promoter is a tissue-specific promoter.
27. The composition of claim 16 , wherein the C-terminal portion of the otoferlin protein is between 30 amino acids to 1600 amino acids in length.
28. The composition of claim 16 , wherein the otoferlin protein is an otoferlin isoform 5 protein.
29. The composition of claim 16 , further comprising a pharmaceutically acceptable excipient.