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慢性疼痛基因治疗发展的一种机制性方法。

A Mechanistic Approach to the Development of Gene Therapy for Chronic Pain.

作者信息

Kibaly C, Loh H H, Law P-Y

机构信息

Department of Pharmacology and Basic Research Center on Molecular and Cell Biology of Drug Addiction, University of Minnesota, Minneapolis, MN, United States.

Department of Pharmacology and Basic Research Center on Molecular and Cell Biology of Drug Addiction, University of Minnesota, Minneapolis, MN, United States.

出版信息

Int Rev Cell Mol Biol. 2016;327:89-161. doi: 10.1016/bs.ircmb.2016.06.002. Epub 2016 Jul 30.

Abstract

Treatment of chronic pain has created a "silent epidemic," a term that describes the serious public health problem of the abuse of opioid painkillers and other prescription drugs. Conventional pharmacotherapy is limited by the loss of effectiveness in the long-term and by potentially lethal side effects. Efforts need to be focused on the development of nonpharmacological approaches. As significant progress is made in the viral vector technology, gene therapy involving recombinant viruses as vehicles may become a viable alternative for treatment of severe pain. Virus-based gene therapy has several advantages: (1) the transfer of a therapeutic gene to produce/release bioactive therapeutic molecules in a specific location in the nervous system thus minimizing the risks of off-target side effects, and (2) sustained long-term production of the therapeutic agent. This review compiles recently developed strategies for gene therapy targeting specific mechanisms of specific chronic pain conditions. A few successful studies on animal models of chronic pain have been translated to human clinical trials.

摘要

慢性疼痛的治疗引发了一场“隐性流行病”,这一术语描述了阿片类止痛药及其他处方药滥用这一严重的公共卫生问题。传统药物疗法存在长期疗效丧失及潜在致命副作用的局限性。需要将努力集中在非药物疗法的开发上。随着病毒载体技术取得重大进展,以重组病毒为载体的基因治疗可能成为治疗重度疼痛的可行替代方法。基于病毒的基因治疗有几个优点:(1)将治疗性基因转移至神经系统特定位置以产生/释放生物活性治疗分子,从而将脱靶副作用风险降至最低;(2)治疗剂的长期持续产生。本综述汇编了针对特定慢性疼痛状况的特定机制的基因治疗最新开发策略。一些关于慢性疼痛动物模型的成功研究已转化为人体临床试验。

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