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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Bibliografische Detailangaben

Veröffentlicht in:	J Virol
Hauptverfasser:	Sarukhan, Adelaida, Camugli, Sabine, Gjata, Bernard, von Boehmer, Harald, Danos, Olivier, Jooss, Karin
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	American Society for Microbiology (ASM) 2001
Schlagworte:	Gene Therapy
Online-Zugang:	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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