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Rationally engineered novel AAV capsids for intra-articular gene delivery

Intra-articular adeno-associated virus (AAV) gene therapy has been explored as a potential strategy for joint diseases. However, concerns of low transduction efficacy, off-target expression, and neutralizing antibodies (Nabs) still need to be addressed. In this study, we demonstrated that AAV6 was t...

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Bibliografiske detaljer
Principais autores: Wenjun Li, Susi Liu Feng, Lizette Herrschaft, R. Jude Samulski, Chengwen Li
Format: Artigo
Sprog:Inglês
Udgivet: Elsevier 2024-03-01
Serier:Molecular Therapy: Methods & Clinical Development
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Online adgang:http://www.sciencedirect.com/science/article/pii/S2329050124000275
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