Successful Interference with Cellular Immune Responses to Immunogenic Proteins Encoded by Recombinant Viral Vectors

Vectors derived from the adeno-associated virus (AAV) have been successfully used for the long-term expression of therapeutic genes in animal models and patients. One of the major advantages of these vectors is the absence of deleterious immune responses following gene transfer. However, AAV vectors...

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Detalhes bibliográficos

Publicado no:	J Virol
Principais autores:	Sarukhan, Adelaida, Camugli, Sabine, Gjata, Bernard, von Boehmer, Harald, Danos, Olivier, Jooss, Karin
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Microbiology (ASM) 2001
Assuntos:	Gene Therapy
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC113921/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11119597/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/JVI.75.1.269-277.2001
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