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Myocardial infarction creates a critical time window for AAV-based cardiac gene transfer

  • Gonglie Chen
  • , Yueyang Zhang
  • , Zhanzhao Liu
  • , Jingdong Wu
  • , Zhan Chen
  • , Luzi Yang
  • , Junxia Zhang
  • , Yufei Wu
  • , Jiting Li
  • , Baochen Bai
  • , Zhengyuan Lv
  • , Fei Gao
  • , Erdan Dong
  • , Yuxuan Guo
  • Peking University Health Science Center
  • Peking University
  • Peking University
  • Capital Medical University
  • Beijing Key Laboratory of Cardiovascular Receptors Research

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Approaches to enhance adeno-associated virus (AAV)-based cardiac gene transfer are the key to successful cardiac gene therapy, but factors influencing AAV transduction remain poorly investigated. This study showed that myocardial infarction (MI) enhanced cardiac AAV transduction, peaking at the third day post-MI in mice. The excessive AAV enrichment at the border zone is due to local vascular permeabilization and cardiomyocyte metabolic remodeling, which is independent of AAV dosage, serotypes and promoters. This effect was harnessed to boost cardiac base editing and improve the outcome of gene therapy for MI in mice. Thus, heart disease itself is a non-negligible factor that alters AAV-based cardiac gene transfer, which provides a new inroad to develop approaches to enhance cardiac gene therapy.

Original languageEnglish
JournalFundamental Research
DOIs
StateAccepted/In press - 2025

Keywords

  • Adeno-associated virus
  • Gene delivery
  • Gene editing
  • Gene therapy
  • Myocardial infarction

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