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Cell-Mediated Immunity to AAV Vectors, Evolving Concepts and Potential Solutions
Adeno-associated virus (AAV) vectors are one of the most efficient in vivo gene delivery platforms. Over the past decade, clinical trials of AAV vector-mediated gene transfer led to some of the most exciting results in the field of gene therapy and, recently, to the market approval of an AAV-based d...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4107954/ https://ncbi.nlm.nih.gov/pubmed/25101090 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fimmu.2014.00350 |
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