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Автор McCarty, Douglas M.
Автор Young, Samuel M.
Автор Samulski, R. Jude
Дата выпуска 2004
dc.description ▪ Abstract  The driving interest in adeno-associated virus (AAV) has been its potential as a gene delivery vector. The early observation that AAV can establish a latent infection by integrating into the host chromosome has been central to this interest. However, chromosomal integration is a two-edged sword, imparting on one hand the ability to maintain the therapeutic gene in progeny cells, and on the other hand, the risk of mutations that are deleterious to the host. A clearer understanding of the mechanism and efficiency of AAV integration, in terms of contributing viral and host-cell factors and circumstances, will provide a context in which to evaluate these potential benefits and risks. Research to date suggests that AAV integration in any context is inefficient, and that the persistence of AAV gene delivery vectors in tissues is largely attributable to episomal genomes.
Формат application.pdf
Издатель Annual Reviews
Копирайт Annual Reviews
Название INTEGRATION OF ADENO-ASSOCIATED VIRUS (AAV) AND RECOMBINANT AAV VECTORS
DOI 10.1146/annurev.genet.37.110801.143717
Print ISSN 0066-4197
Журнал Annual Review of Genetics
Том 38
Первая страница 819
Последняя страница 845
Аффилиация McCarty, Douglas M.; School of Pharmacy, University of North Carolina, Chapel Hill, North Carolina 27599

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