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丙型肝炎病毒的抗病毒耐药性及特异性靶向治疗(STAT-C)

Antiviral resistance and specifically targeted therapy for HCV (STAT-C).

作者信息

Thompson A J V, McHutchison J G

机构信息

Division of Gastroenterology/Hepatology, Duke Clinical Research Institute, Duke University, Durham, NC, USA.

出版信息

J Viral Hepat. 2009 Jun;16(6):377-87. doi: 10.1111/j.1365-2893.2009.01124.x.

Abstract

As health care providers, we find ourselves on the verge of a new era in the treatment of chronic hepatitis C virus (HCV) infection. A number of directly acting antiviral agents are now in the latter stages of clinical development. The more promising candidates include direct inhibitors of the HCV nonstructural 3 protease, as well as both nucleoside and non-nucleoside inhibitors of the NS5B RNA-dependent RNA polymerase. Although these agents have demonstrated potent antiviral effect, monotherapy has been complicated by rapid virological breakthrough due to the selection of drug-resistant mutants. As for HIV and HBV, combination therapy will therefore be necessary. This brief review summarizes the current literature concerning resistance and directly acting antiviral agents, and identifies key challenges facing this emerging field.

摘要

作为医疗服务提供者,我们发现自己正处在慢性丙型肝炎病毒(HCV)感染治疗新时代的边缘。目前,一些直接作用抗病毒药物正处于临床开发的后期阶段。较有前景的候选药物包括HCV非结构3蛋白酶的直接抑制剂,以及NS5B RNA依赖性RNA聚合酶的核苷类和非核苷类抑制剂。尽管这些药物已显示出强大的抗病毒效果,但由于耐药突变体的选择,单药治疗因病毒学快速突破而变得复杂。因此,与治疗HIV和HBV一样,联合治疗将是必要的。本简要综述总结了有关耐药性和直接作用抗病毒药物的当前文献,并确定了这一新兴领域面临的关键挑战。

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