| Literature DB >> 36002664 |
Fan Wu1,2, Kumar Sambamurti3, Suhua Sha4.
Abstract
Adeno-associated viruses (AAVs) are viral vectors that offer an excellent platform for gene therapy due to their safety profile, persistent gene expression in non-dividing cells, target cell specificity, lack of pathogenicity, and low immunogenicity. Recently, gene therapy for genetic hearing loss with AAV transduction has shown promise in animal models. However, AAV transduction for gene silencing or expression to prevent or manage acquired hearing loss is limited. This review provides an overview of AAV as a leading gene delivery vector for treating genetic hearing loss in animal models. We highlight the advantages and shortcomings of AAV for investigating the mechanisms and preventing acquired hearing loss. We predict that AAV-mediated gene manipulation will be able to prevent acquired hearing loss.Entities:
Keywords: AAV transduction in vivo; AAV-mediated gene therapy; Acquired hearing loss
Year: 2022 PMID: 36002664 DOI: 10.1007/s10162-022-00866-y
Source DB: PubMed Journal: J Assoc Res Otolaryngol ISSN: 1438-7573