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 plurality of AAV vectors comprising:
a) a first AAV vector comprising an inverted terminal repeat (ITR) and a promoter operably linked to a portion of a gene encoding a human otoferlin isoform 5 polypeptide; and
b) a second AAV vector comprising an inverted terminal repeat (ITR), a portion of the gene encoding the human otoferlin isoform 5 polypeptide and a polyadenylation sequence;
wherein the first AAV vector and the second AAV vector independently contain packaging capacity of less than about 6 kb; and wherein the first AAV vector and the second AAV vector are capable of constituting a full-length otoferlin messenger RNA in a target cell.
2. The plurality of AAV vectors of claim 1 , wherein the promoter is a constitutive promoter.
3. The plurality of AAV vectors of claim 1 , wherein the promoter is selected from the group consisting of a CBA, a CMV, a CB7, or a Cochlea-specific promoter.
4. The plurality of AAV vectors of claim 1 , wherein the first AAV vector further comprises an enhancer, an intron, or a combination thereof.
5. The plurality of AAV vectors of claim 1 , wherein the first AAV vector and the second AAV vector each comprise 5′ and 3′ AAV2 ITRs.
6. The plurality of AAV vectors of claim 1 , wherein the first AAV vector and the second AAV vector are encapsulated by AAV capsids, wherein the AAV capsids are AAV serotype 1, 2, 3, 4, 5, 6, 7, 8, 9, rh8, rh10, rh39, rh43, or Anc80.
7. The plurality of AAV vectors of claim 1 , wherein the first and second AAV vectors are encapsulated by Anc80 capsids.
8. The plurality of AAV vectors of claim 1 , wherein the target cell is a cell of the inner ear.
9. The plurality of AAV vectors of claim 1 , wherein the first AAV vector comprises a first splicing signal and the second AAV vector comprises a second splicing signal.
10. A plurality of AAV vectors comprising:
a) a first AAV vector comprising a promoter operably linked to a portion of a gene encoding a human otoferlin isoform 5 polypeptide; and
b) a second AAV vector comprising a portion of the gene encoding the human otoferlin isoform 5 polypeptide and a polyadenylation sequence;
wherein the first AAV vector and the second AAV vector each comprise an AAV2 ITR; and
wherein the first AAV vector and the second AAV vector are capable of constituting a full-length otoferlin messenger RNA in a target cell.
11. The plurality of AAV vectors of claim 10 , wherein the promoter is a constitutive promoter.
12. The plurality of AAV vectors of claim 10 , wherein the promoter is selected from the group consisting of a CBA, a CMV, a CB7, or a Cochlea-specific promoter.
13. The plurality of AAV vectors of claim 10 , wherein the first AAV vector further comprises an enhancer, an intron, or a combination thereof.
14. The plurality of AAV vectors of claim 10 , wherein the first and second AAV vectors are encapsulated by AAV capsids, wherein the AAV capsids are AAV serotype 1, 2, 3, 4, 5, 6, 7, 8, 9, rh8, rh10, rh39, rh43, or Anc80.
15. The plurality of AAV vectors of claim 10 , wherein the first and second AAV vectors are encapsulated by Anc80 capsids.
16. A composition comprising:
a) a first recombinant AAV vector (rAAV) which is packaged into a capsid protein, wherein the first rAAV comprises a promoter operably linked to a portion of a gene encoding a human otoferlin isoform 5 polypeptide, a 5′ ITR and a 3′ ITR; and
b) a second rAAV which is packaged into a capsid protein, wherein the second rAAV comprises a portion of the gene encoding the human otoferlin isoform 5 polypeptide, a polyadenylation sequence, a 5′ ITR and a 3′ ITR;
wherein the first rAAV and the second rAAV are capable of constituting a full-length otoferlin messenger RNA in a target cell.
17. The composition of claim 16 wherein the promoter is a constitutive promoter.
18. The composition of claim 16 , wherein the promoter is selected from the group consisting of a CBA, a CMV, a CB7, or a Cochlea-specific promoter.
19. The composition of claim 16 , wherein the first rAAV further comprises an enhancer, an intron, or a combination thereof.
20. The composition of claim 16 , wherein the first rAAV and the second rAAV independently contain packaging capacity of less than about 6 kb.
21. The composition of claim 16 , wherein the first rAAV and the second rAAV each comprise 5′ and 3′ AAV2 ITRs.
22. The composition of claim 16 , wherein the capsid proteins are AAV serotype 1, 2, 3, 4, 5, 6, 7, 8, 9, rh8, rh10, rh39, rh43, or Anc80.
23. The composition of claim 16 , wherein the capsid proteins are Anc80 capsids.
24. The composition of claim 16 , wherein the target cell is a mammalian cell.
25. The composition of claim 16 , wherein the target cell is a cell of the inner ear.
26. The composition of claim 16 , wherein the first rAAV comprises a first splicing signal and the second rAAV comprise a second splicing signal.
27. The composition of claim 16 , which is formulated for intra-cochlear administration.
28. The composition of claim 16 , wherein the promoter is an inducible promoter.
29. The composition of claim 16 , wherein the promoter is a tissue-specific promoter.