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丙型肝炎病毒的新药

New drugs for hepatitis C virus.

作者信息

Pockros Paul J

机构信息

Division of Gastroenterology/Hepatology, Scripps Clinic, The Scripps Research Institute, 10666 N. Torrey Pines Road, La Jolla, CA 92037, USA.

出版信息

Expert Rev Gastroenterol Hepatol. 2007 Oct;1(1):145-54. doi: 10.1586/17474124.1.1.145.

Abstract

No new therapy has been approved for the treatment of chronic hepatitis C in the last 5 years in the USA since the approval of pegylated interferon (IFN)-alpha(2a) and ribavirin. Multiple new drugs are currently in development and are expected to be approved for use in the USA and/or the EU by 2011-2013. Although the mechanism of action of pegylated IFN and ribavirin are not completely known, it is likely that they will continue to be used in combination regimens for a number of years. Direct antivirals are likely to be the first new drugs to be used in combination with pegylated IFN and ribavirin. Viral resistance will prove to be a significant barrier and require that consolidation therapy with at least 24 weeks of pegylated IFN and ribavirin be used to successfully prevent the selection or emergence of resistant variants. Numerous other compounds, such as ribavirin analogs, long-acting IFNs, hepatoprotectants and immunomodulators, are in development and may replace the drugs that are used currently. The combination of direct antivirals, such as protease and polymerase inhibitors, may rapidly follow in development, as has occurred in HIV drug therapy.

摘要

自从聚乙二醇化干扰素(IFN)-α(2a)和利巴韦林获批以来,过去5年美国尚未批准用于治疗慢性丙型肝炎的新疗法。目前有多种新药正在研发中,预计到2011 - 2013年将在美国和/或欧盟获批使用。虽然聚乙二醇化干扰素和利巴韦林的作用机制尚不完全清楚,但它们可能会在联合用药方案中继续使用数年。直接抗病毒药物可能是首批与聚乙二醇化干扰素和利巴韦林联合使用的新药。病毒耐药性将被证明是一个重大障碍,这就需要使用至少24周的聚乙二醇化干扰素和利巴韦林进行巩固治疗,以成功预防耐药变异株的选择或出现。许多其他化合物,如利巴韦林类似物、长效干扰素、肝保护剂和免疫调节剂,正在研发中,可能会取代目前使用的药物。直接抗病毒药物的联合使用,如蛋白酶和聚合酶抑制剂,可能会迅速跟进研发,就像HIV药物治疗中那样。

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