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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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | angličtina |
| Vydáno: |
2001
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| On-line přístup: | https://doi.org/10.1128/jvi.75.1.269-277.2001 |
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