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针对病毒的RNA干扰:攻击与反击

RNA interference against viruses: strike and counterstrike.

作者信息

Haasnoot Joost, Westerhout Ellen M, Berkhout Ben

机构信息

Laboratory of Experimental Virology, Department of Medical Microbiology, Center for Infection and Immunity Amsterdam, Academic Medical Center of University of Amsterdam, Meibergdreef 15, 1105 AZ Amsterdam, The Netherlands.

出版信息

Nat Biotechnol. 2007 Dec;25(12):1435-43. doi: 10.1038/nbt1369.

Abstract

RNA interference (RNAi) is a conserved sequence-specific, gene-silencing mechanism that is induced by double-stranded RNA. RNAi holds great promise as a novel nucleic acid-based therapeutic against a wide variety of diseases, including cancer, infectious diseases and genetic disorders. Antiviral RNAi strategies have received much attention and several compounds are currently being tested in clinical trials. Although induced RNAi is able to trigger profound and specific inhibition of virus replication, it is becoming clear that RNAi therapeutics are not as straightforward as we had initially hoped. Difficulties concerning toxicity and delivery to the right cells that earlier hampered the development of antisense-based therapeutics may also apply to RNAi. In addition, there are indications that viruses have evolved ways to escape from RNAi. Proper consideration of all of these issues will be necessary in the design of RNAi-based therapeutics for successful clinical intervention of human pathogenic viruses.

摘要

RNA干扰(RNAi)是一种由双链RNA诱导的保守的序列特异性基因沉默机制。RNAi作为一种新型的基于核酸的疗法,有望治疗包括癌症、传染病和遗传疾病在内的多种疾病。抗病毒RNAi策略备受关注,目前有几种化合物正在进行临床试验。尽管诱导的RNAi能够引发对病毒复制的深度特异性抑制,但越来越明显的是,RNAi疗法并不像我们最初希望的那样简单。早期阻碍基于反义疗法发展的毒性和向正确细胞递送方面的困难,也可能适用于RNAi。此外,有迹象表明病毒已经进化出逃避RNAi的方法。在设计基于RNAi的疗法以成功临床干预人类致病病毒时,必须适当考虑所有这些问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c5/7096910/aaa5180e24fb/41587_2007_Article_BFnbt1369_Fig1_HTML.jpg

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