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Capsid-expressing DNA in AAV vectors and its elimination by use of an oversize capsid gene for vector production
Adeno-associated virus vectors have been shown to mediate persistent transduction in animal models of gene therapy. However, clinical trials with AAV vectors have shown that an immune response to AAV capsid protein can result in clearance of transduced cells. One source of capsid antigen is from the...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3072450/ https://www.ncbi.nlm.nih.gov/pubmed/21160534 http://dx.doi.org/10.1038/gt.2010.167 |