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

ABSTRACT 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, AA...

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Bibliográfalaš dieđut
Váldodahkkit: Adélaïda Sarukhan, Sabine Camugli, Bernard Gjata, Harald von Boehmer, Olivier Danos, Karin Jooss
Materiálatiipa: Artigo
Giella:eaŋgalasgiella
Almmustuhtton: 2001
Liŋkkat:https://doi.org/10.1128/jvi.75.1.269-277.2001
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