ADENO-ASSOCIATED VIRUS VARIANT CAPSIDS WITH IMPROVED RETINAL TRANSDUCTION AND USES THEREOF
Provided herein are variant adeno-associated virus (AAV) capsid proteins having one or more modifications in amino acid sequence relative to a parental AAV capsid protein, which, when present in an AAV virion, confer increased infectivity of one or more types of retinal cells as compared to the infectivity of the retinal cells by an AAV virion comprising the unmodified parental AAV capsid protein. Also provided are recombinant AAV virions and pharmaceutical compositions thereof comprising a variant AAV capsid protein as described herein, methods of making these rAAV capsid proteins and virions, and methods for using these rAAV capsid proteins and virions in research and clinical practice, for example in, e.g., the delivery of nucleic acid sequences to one or more cells of the retina for the treatment of retinal disorders and diseases.
1 . A method of delivering a nucleic acid encoding aflibercept to a retinal cell of a human subject, the method comprising intravitreally administering to the human subject a dose of 4×10 10 to 1×10 12 vector genomes (vg) of a recombinant adeno-associated virus (rAAV), the rAAV comprising (a) the nucleic acid encoding aflibercept, operatively linked to a constitutive promoter and (b) a protein comprising an amino acid sequence at least 95% identical to SEQ ID NO: 42.
2 . The method according to claim 1 , wherein the rAAV comprises a polyadenylation signal.
3 . The method according to claim 1 , wherein the rAAV comprises ITRs from AAV2.
4 . The method according to claim 1 , wherein the protein comprises an amino acid sequence at least 96% identical to SEQ ID NO: 42.
5 . The method according to claim 1 , wherein the protein comprises an amino acid sequence at least 97% identical to SEQ ID NO: 42.
6 . The method according to claim 1 , wherein the protein comprises an amino acid sequence at least 98% identical to SEQ ID NO: 42.
7 . The method according to claim 1 , wherein the constitutive promoter is a cytomegalovirus promoter (CMV), a CMV early enhancer/chicken β-actin (CBA) promoter/rabbit β-globin intron (CAG), a CBSB promoter, a human elongation factor 1α promoter (EF1α), a human phosphoglycerate kinase promoter (PGK), a mitochondrial heavy-strand promoter or a ubiquitin promoter.
7 . The method according to claim 1 , wherein the constitutive promoter is a CMV promoter.
8 . The method according to claim 1 , wherein the retinal cell is a retinal pigment epithelium (RPE) and/or photoreceptor cell.