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- W2072283703 abstract "Despite significant advancements with recombinant AAV2 or AAV8 vectors for liver directed gene therapy in humans, it is well-recognized that host and vector-related immune challenges need to be overcome for long-term gene transfer. To overcome these limitations, alternate AAV serotypes (1-10) are being rigorously evaluated. AAV5 is the most divergent (55% similarity vs. other serotypes) and like AAV1 vector is known to transduce liver efficiently. AAV1 and AAV5 vectors are also immunologically distinct by virtue of their low seroprevalence and minimal cross reactivity against pre-existing AAV2 neutralizing antibodies. Here, we demonstrate that targeted bio-engineering of these vectors, augment their gene expression in murine hepatocytes in vivo (up to 16-fold). These studies demonstrate the feasibility of the use of these novel AAV1 and AAV5 vectors for potential gene therapy of diseases like hemophilia." @default.
- W2072283703 created "2016-06-24" @default.
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- W2072283703 date "2013-05-13" @default.
- W2072283703 modified "2023-09-30" @default.
- W2072283703 title "Improved adeno-associated virus (AAV) serotype 1 and 5 vectors for gene therapy" @default.
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- W2072283703 doi "https://doi.org/10.1038/srep01832" @default.
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