Chemical approaches to probe and engineer AAV vectors

Abstract

Adeno-associated virus (AAV) has emerged as the most promising vector for in vivo human gene therapy, with several therapeutic approvals in the last few years and countless more under development. Underlying this remarkable success are several attractive features that AAV offers, including lack of pathogenicity, low immunogenicity, long-term gene expression without genomic integration, the ability to infect both dividing and non-dividing cells, etc. However, the commonly used wild-type AAV capsids in therapeutic development present significant challenges, including inadequate tissue specificity and the need for large doses to attain therapeutic effectiveness, raising safety concerns. Additionally, significant preexisting adaptive immunity against most natural capsids, as well as the development of such anti-capsid immunity after the first treatment, represent major challenges. Strategies to engineer the AAV capsid are critically needed to address these challenges and unlock the full promise of AAV gene therapy. Chemical modification of the AAV capsid has recently emerged as a powerful new approach to engineer its properties. Unlike genetic strategies, which can be more disruptive to the delicate capsid assembly and packaging processes, “late-stage” chemical modification of the assembled capsid — whether at natural amino acid residues or site-specifically installed noncanonical amino acid residues — often enables a versatile approach to introducing new properties to the capsid. This review summarizes the significant recent progress in AAV capsid engineering strategies, with a particular focus on chemical modifications in advancing the next generation of AAV-based gene therapies

Article information

Article type
Minireview
Submitted
24 mar 2024
Accepted
14 jun 2024
First published
18 jun 2024
This article is Open Access
Creative Commons BY-NC license

Nanoscale, 2024, Accepted Manuscript

Chemical approaches to probe and engineer AAV vectors

Q. Pham, J. Glicksman and A. Chatterjee, Nanoscale, 2024, Accepted Manuscript , DOI: 10.1039/D4NR01300J

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