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用于治疗心力衰竭的基因疗法:希望延迟。

Gene therapy for the treatment of heart failure: promise postponed.

作者信息

Hulot Jean-Sebastien, Ishikawa Kiyotake, Hajjar Roger J

机构信息

Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, Box 1030, New York, NY 10029-6574, USA Sorbonne Universités, UPMC University Paris 06, AP-HP, Institute of Cardiometabolism and Nutrition (ICAN), Pitié-Salpêtrière Hospital, F-75013 Paris, France.

Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, Box 1030, New York, NY 10029-6574, USA.

出版信息

Eur Heart J. 2016 Jun 1;37(21):1651-8. doi: 10.1093/eurheartj/ehw019. Epub 2016 Feb 27.

Abstract

Gene therapy has emerged as a powerful tool in targeting the molecular mechanisms implicated in heart failure. Refinements in vector technology, including the development of recombinant adeno-associated vectors, have allowed for safe, long-term, and efficient gene transfer to the myocardium. These advancements, coupled with evolving delivery techniques, have placed gene therapy as a viable therapeutic option for patients with heart failure. However, after much promise in early-phase clinical trials, the more recent larger clinical trials have shown disappointing results, thus forcing the field to re-evaluate current vectors, delivery systems, targets, and endpoints. We provide here an updated review of current cardiac gene therapy programmes that have been or are being translated into clinical trials.

摘要

基因治疗已成为一种针对心力衰竭相关分子机制的强大工具。载体技术的改进,包括重组腺相关载体的开发,使得能够安全、长期且高效地将基因导入心肌。这些进展,再加上不断发展的递送技术,使基因治疗成为心力衰竭患者可行的治疗选择。然而,在早期临床试验取得诸多成果后,最近规模更大的临床试验结果却令人失望,这迫使该领域重新评估当前的载体、递送系统、靶点和终点指标。我们在此提供对已开展或正在开展临床试验的当前心脏基因治疗方案的最新综述。

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