Cited by 234Virus-based gene therapy researchCardiac electrophysiology and arrhythmiasCardiac Fibrosis and Remodeling

Cardiac AAV9-S100A1 gene therapy rescues post-ischemic heart failure in a preclinical large animal model

Open access
Pleger, Sven T., Shan, Changguang, Ksienzyk, Jan, Bekeredjian, Raffi, Boekstegers, Peter, Hinkel, Rabea, Schinkel, Stefanie, Leuchs, Barbara +8 more·2011·Science Translational Medicine

Abstract

A protein that regulates cellular calcium, delivered percutaneously to the heart by gene therapy, improves cardiac function in pigs with heart failure and may also be effective in humans.

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Crossref · 10.1126/scitranslmed.3002097

Cites

49 of 49 references verified0 citation errors · 0 not checkable

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  • Successful cardiac transduction in large species requires surgical and catheter-based approaches that preferentially target the heart.

    “Successful cardiac transduction in large species requires surgical and catheter-based approaches that can preferentially target the heart”
  • Heart failure can be induced in swine by rapid pacing and myocardial infarction.

    “Heart failure can be induced in swine by a variety of methods such as rapid pacing (Lacroix, et al., 2002) and myocardial infarction (Pleger, et al., 2011).”
  • Myocardial gene deliveries have been performed in swine with AAVs using methods that deliver vectors preferentially to the myocardium such as myocardial injections, direct intracoronary, and selective retroinfusion coupled with coronary artery occlusion.

    “Myocardial gene deliveries have been performed with the aid of AAVs with methods that deliver the vectors preferentially to the myocardium such as myocardial injections (H. Su, et al., 2008), direct intracoronary (Kaspar, et al., 2005), and selective retroinfusion coupled with coronary artery occlusion (Pleger, et al., 2011; Raake, et al., 2008).”

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Authors
Pleger, S. T., Shan, C., Ksienzyk, J., Bekeredjian, R., Boekstegers, P., Hinkel, R., Schinkel, S., Leuchs, B., Ludwig, J., Qiu, G., Weber, C., Raake, P., Koch, W. J., Katus, H. A., Müller, O. J., & Most, P.
Affiliations
  • Heidelberg University (DE)
  • LMU Klinikum (DE)
  • German Cancer Research Center (DE)
  • Thomas Jefferson University (US)
Corresponding author
  • Müller, Oliver J.
  • Most, Patrick
Venue
Science Translational Medicine
Published
2011-07-20
Volume
3
Issue
92
Pages
92ra64-92ra64
ISSN
  • 1946-6234 (ISSN-L)
  • 1946-6242
OpenAlex
W2110557028
Cited by
234
References
49
Citations by year
2026: 5 · 2025: 10 · 2024: 10 · 2023: 10 · 2022: 14 · 2021: 15 · 2020: 17 · 2019: 16 · 2018: 14 · 2017: 16 · 2016: 19 · 2015: 22 · 2014: 15 · 2013: 22 · 2012: 24
FWCI
12.97
Type
journal article
Language
en
Open access
Locations
  • Science Translational Medicine (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • OPUS (Augsburg University) (submittedVersion)
Funders
National Heart, Lung, and Blood Institute (R01 HL 56205, R01HL061690, R01HL92130-02S1, R01HL056205, R01 HL92130, R01HL092130, P01HL075443)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac electrophysiology and arrhythmias
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Fibrosis and Remodeling
Keywords
S100A1, AAV9 gene therapy, cardiac gene therapy, heart failure, myocardial infarction, coronary artery occlusion, sarcoplasmic reticulum calcium handling, cardiac contractility, left ventricular remodeling, energy homeostasis, domestic pigs
MeSH terms
Dependovirus, Animals, Calcium, Disease Models, Animal, Energy Metabolism, Heart Failure, Heart Function Tests, Homeostasis, Humans, Myocardial Infarction, Myocardium, S100 Proteins, Organ Specificity, Sarcoplasmic Reticulum, Genetic Therapy, Biomarkers, Myocardial Ischemia, Gene Transfer Techniques, Myocytes, Cardiac, Sus scrofa

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