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基因疗法在勃起功能障碍(ED)治疗中的应用:过去、现在与未来。

Gene therapy in the management of erectile dysfunction (ED): past, present, and future.

作者信息

Melman Arnold, Davies Kelvin P

机构信息

Department of Urology, Albert Einstein College of Medicine, Bronx, NY, USA.

出版信息

ScientificWorldJournal. 2009 Aug 31;9:846-54. doi: 10.1100/tsw.2009.102.

Abstract

In the past, many researchers considered viral vectors to be the most promising candidates to transfer genetic material into the corpora for the treatment of erectile dysfunction. However, at present, no viral vectors have progressed to human trials. In contrast, the use of naked gene therapy, a plasmid expressing the human Maxi-K potassium channel, is the only gene therapy treatment to be evaluated in clinical phase I trials to date. The success of these studies, proving the safety of this treatment, has paved the way for the development of future gene transfer techniques based on similar transfer methods, as well as novel treatment vectors, such as stem cell transfer.

摘要

过去,许多研究人员认为病毒载体是将遗传物质导入阴茎海绵体以治疗勃起功能障碍最有前景的候选者。然而,目前尚无病毒载体进入人体试验阶段。相比之下,裸基因疗法,即一种表达人类大电导钙激活钾通道(Maxi-K)的质粒,是迄今为止唯一进入I期临床试验评估的基因治疗方法。这些研究证明了该疗法的安全性,为基于类似导入方法的未来基因转移技术以及新型治疗载体(如干细胞移植)的发展铺平了道路。

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Gene therapy as future treatment of erectile dysfunction.基因治疗:未来治疗勃起功能障碍的新方法
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