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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Sarukhan, Adelaida, Camugli, Sabine, Gjata, Bernard, von Boehmer, Harald, Danos, Olivier, Jooss, Karin
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: American Society for Microbiology 2001
Pynciau:
Gene Therapy
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC113921/
https://ncbi.nlm.nih.gov/pubmed/11119597
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/JVI.75.1.269-277.2001
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