Phase 1 gene therapy for Duchenne muscular dystrophy using a translational optimized AAV vector

Bowles et al. (2012). Mol Ther DOI: 10.1038/mt.2011.237 Citations: 516

Key findings

AAV2.5T is a chimeric serotype combining AAV2 and AAV5 capsid sequences. Enhanced muscle transduction efficiency with improved spread compared to AAV2 or AAV5 alone. Demonstrated therapeutic efficacy in DMD preclinical models.

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