A comprehensive study of AAV tropism across C57BL/6 mice, BALB/c mice, and crab-eating macaques

Recombinant adeno-associated viruses (AAVs) have been widely used for gene delivery and gene therapy. However, certain AAV serotypes exhibited distinct transduction patterns among different mouse strains or between mice and non-human primates (NHPs). These variations prompted us to investigate the AAV tropism of 21 capsid variants using barcoded AAV libraries among different tissues in C57BL/6 and BALB/c mice, as well as in crab-eating macaques. Our study unveiled that AAV tropisms varied significantly among different mouse strains and species, particularly in capsid variants such as AAV4, AAV9, PHP.B, and CAP-B10. Notably, AAV4 exhibited liver-detargeting properties in both mice and NHPs, and was remarkably efficient in transducing the lung, glomerulus, and pancreatic islet. These findings furnish crucial insights into the variations of AAV tropism among different mouse strains and species and facilitate the selection of appropriate AAV capsids for target tissues among different mouse strains and in NHPs.

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Publication Details

Journal
Molecular Therapy — Methods & Clinical Development
Published
2025-02-13
DOI
https://doi.org/10.1016/j.omtm.2025.101434
Citations
8
Primary Topic
Virus-based gene therapy research
Type
article
Field-Weighted Citation Impact
14.54

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article

A comprehensive study of AAV tropism across C57BL/6 mice, BALB/c mice, and crab-eating macaques

Renrong Wu, Xiaoming Yang, Xinyu Liu, Canbin Feng et al.
8 citations
Molecular Therapy — Methods & Clinical Development
Virus-based gene therapy research
14.54
article

A comprehensive study of AAV tropism across C57BL/6 mice, BALB/c mice, and crab-eating macaques

Renrong Wu, Xiaoming Yang, Xinyu Liu, Canbin Feng, Kailun Fang, Guannan Geng, Fan Yang, Yuanhua Liu, Junhui Xia, Linyu Shi, Hui Yang
article en
8 citations

Abstract

Recombinant adeno-associated viruses (AAVs) have been widely used for gene delivery and gene therapy. However, certain AAV serotypes exhibited distinct transduction patterns among different mouse strains or between mice and non-human primates (NHPs). These variations prompted us to investigate the AAV tropism of 21 capsid variants using barcoded AAV libraries among different tissues in C57BL/6 and BALB/c mice, as well as in crab-eating macaques. Our study unveiled that AAV tropisms varied significantly among different mouse strains and species, particularly in capsid variants such as AAV4, AAV9, PHP.B, and CAP-B10. Notably, AAV4 exhibited liver-detargeting properties in both mice and NHPs, and was remarkably efficient in transducing the lung, glomerulus, and pancreatic islet. These findings furnish crucial insights into the variations of AAV tropism among different mouse strains and species and facilitate the selection of appropriate AAV capsids for target tissues among different mouse strains and in NHPs.

Molecular Therapy — Methods & Clinical DevelopmentVol. 33(1)
Center for Excellence in Brain Science and Intelligence Technology (CN), Eye & ENT Hospital of Fudan University (CN), NewGen Therapeutics (United States) (US)
National Natural Science Foundation of China, Chinese Academy of Sciences, Science and Technology Commission of Shanghai Municipality
Zero hunger
Openalex Percentile: Top 1%
Virus-based gene therapy research
14.54
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