Various AAV Serotypes and Their Applications in Gene Therapy: An Overview

Shaza S. Issa, Alisa A. Shaimardanova, Valeriya V. Solovyeva, Albert Anatolyevich Rizvanov

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Abstract

Despite scientific discoveries in the field of gene and cell therapy, some diseases still have no effective treatment. Advances in genetic engineering methods have enabled the development of effective gene therapy methods for various diseases based on adeno-associated viruses (AAVs). Today, many AAV-based gene therapy medications are being investigated in preclinical and clinical trials, and new ones are appearing on the market. In this article, we present a review of AAV discovery, properties, different serotypes, and tropism, and a following detailed explanation of their uses in gene therapy for disease of different organs and systems.

Abstract of "Various AAV Serotypes and Their Applications in Gene Therapy: An Overview" by Shaza S. Issa, Alisa A. Shaimardanova, Valeriya V. Solovyeva et al., https://doi.org/10.3390/cells12050785, used under its Creative Commons Attribution license (CC-BY); markup removed, otherwise unmodified.

Record

Archive ID
doi:10.3390/cells12050785
Published
Mar 1, 2023
Venue
Cells
DOI
10.3390/cells12050785
PubMed
36899921
Categories
Virus-based gene therapy research
License
cc-by
Provenance
openalex

Topics