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T Cell-Mediated Immune Responses to AAV and AAV Vectors
Adeno-associated virus (AAV)-mediated gene transfer has benefited patients with inherited diseases, such as hemophilia B, by achieving long-term expression of the therapeutic transgene. Nevertheless, challenges remain due to rejection of AAV-transduced cells, which in some, but not all, patients can...
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| Pubblicato in: | Front Immunol |
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| Autore principale: | |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Frontiers Media S.A.
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8076552/ https://ncbi.nlm.nih.gov/pubmed/33927727 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fimmu.2021.666666 |
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