RNA干扰抗病毒治疗:梦想还是现实?

Z. Nizamani, C. Holz, D. Keita, G. Libeau, E. Albina, R. Almeida
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引用次数: 1

摘要

在RNA干扰(RNAi)被发现后不久,其作为有效抗病毒治疗的潜力就被认识到。从那时起,RNAi已经被广泛用于抗病毒目的,可以有效地阻断病毒在体外的复制。然而,对于体内使用,递送问题、毒性、RNAi抑制和病毒逃逸仍然是主要障碍。在这里,我们提供了RNAi策略的概述,并回顾了已经开发的方法,以克服障碍,实现抗病毒和其他治疗的靶向基因沉默。DOI: http://dx.doi.org/10.17525/vrr.v18i1 - 2.92
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RNA INTERFERENCE AS ANTIVIRAL THERAPY: DREAM OR REALITY?
Soon aft er discovery of RNA interference (RNAi), its potential as eff ective antiviral therapy was recognized. Since then RNAi has been variously exploited for antiviral purposes which could eff ectively block viral replication in vitro. For invivo use, however, delivery issue, toxicity, RNAi suppression and viral escape are still major hurdles. Here, we providean overview of the RNAi strategy and review the approaches that have been developed to surpass the obstacles and to achieve targeted gene silencing for antiviral and other therapies. DOI:  http://dx.doi.org/10.17525/vrr.v18i1-2.92
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