J. W. Goethe University Hospital, Department of Internal Medicine I, Theodor-Stern-Kai 7, 60590 Frankfurt am Main, Germany.
Curr Opin Virol. 2012 Oct;2(5):651-5. doi: 10.1016/j.coviro.2012.08.008. Epub 2012 Sep 21.
The approval of direct-acting antiviral agents (DAAs) against the hepatitis C virus (HCV) NS3 protease revolutionized antiviral therapy in chronic hepatitis C. They mark the beginning of an era with drugs designed to inhibit specific viral proteins involved in the virus life cycle rather than the nonspecific antiviral activity of interferon. Upcoming generations of antivirals are expected that lead to viral eradication in most patients who undergo treatment with hope held for years that HCV can be cured without interferon. Antiviral drug resistance plays a key role in DAA-treatment failure. Knowledge on molecular escape mechanisms of resistant variants, their time to wild-type reversal and potential persistence is of upmost importance to design treatment strategies for patients with previous DAA-treatment failure.
直接作用抗病毒药物(DAAs)对丙型肝炎病毒(HCV)NS3 蛋白酶的批准彻底改变了慢性丙型肝炎的抗病毒治疗。它们标志着一个新时代的开始,这个时代的药物旨在抑制病毒生命周期中涉及的特定病毒蛋白,而不是干扰素的非特异性抗病毒活性。预计未来会有新一代的抗病毒药物,使大多数接受治疗的患者能够实现病毒清除,多年来人们一直希望能够在不使用干扰素的情况下治愈丙型肝炎。抗病毒药物耐药性在 DAA 治疗失败中起着关键作用。了解耐药变异体的分子逃逸机制、它们向野生型逆转的时间以及潜在的持续性,对于为以前接受过 DAA 治疗失败的患者设计治疗策略至关重要。