Modified adeno-associated viral capsid proteins for ocular gene therapy and methods of use thereof
Provided herein are modified adeno-associated viral (AAV) capsid proteins, compositions (e.g., rAAV) comprising the capsid proteins, and nucleic acids encoding the capsid proteins. The AAV capsids provided herein confer retinal cell tropism and/or corneal cell tropism, and mediate improved transduct...
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Main Authors | , , , , |
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Format | Patent |
Language | Chinese English |
Published |
16.11.2021
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Subjects | |
Online Access | Get full text |
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Summary: | Provided herein are modified adeno-associated viral (AAV) capsid proteins, compositions (e.g., rAAV) comprising the capsid proteins, and nucleic acids encoding the capsid proteins. The AAV capsids provided herein confer retinal cell tropism and/or corneal cell tropism, and mediate improved transduction efficiency in clinically relevant ocular cell types such as photoreceptors and/or corneal endothelial cells. Also provided are nucleic acids encoding the capsid proteins, and AAV particles comprising the capsid proteins. |
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Bibliography: | Application Number: TW202110103551 |