Anti-AAV Antibodies in AAV Gene Therapy: Current Challenges and Possible Solutions
Adeno-associated virus (AAV) vector-based gene therapy is currently the only in vivo gene therapy approved in the US and Europe. The recent tragic death of three children in a clinical trial to treat X-Linked Myotubular Myopathy by delivering myotubularin with an AAV8 vector notwithstanding, AAV rem...
| Published in: | Frontiers in Immunology |
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| Main Author: | |
| Format: | Article |
| Language: | English |
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Frontiers Media S.A.
2021-03-01
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| Online Access: | https://www.frontiersin.org/articles/10.3389/fimmu.2021.658399/full |
