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...

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Bibliographic Details
Published in:Frontiers in Immunology
Main Author: Thomas Weber
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-03-01
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2021.658399/full