Anti-Hepatitis C Virus Drugs in Development

被引:84
作者
Schaefer, Esperance A. K. [1 ]
Chung, Raymond T. [1 ]
机构
[1] Massachusetts Gen Hosp, Dept Med, Gastrointestinal Unit, Boston, MA 02114 USA
关键词
Protease Inhibitors; NS5B Inhibitors; NS5A Inhibitors; Host Targeted Anti-Virals; REPLICATION COMPLEX INHIBITOR; NS3/4A PROTEASE INHIBITOR; IN-VITRO RESISTANCE; ANTIVIRAL ACTIVITY; INTERFERON-LAMBDA; GENETIC-VARIATION; RNA REPLICATION; COMBINATION THERAPY; NS5A INHIBITOR; HCV;
D O I
10.1053/j.gastro.2012.02.015
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Development of robust cell culture models for hepatitis C viral infection has greatly increased our understanding of this virus and its life cycle. This knowledge has led to the development of many drugs that target specific elements of viral replication, including viral proteins and host factors required for replication. The NS3/4A serine protease inhibitors were the first of these to be used in the clinic, and reagents that target other elements of the viral lifecycle are in advanced stages of clinical development. These include new NS3/4A protease inhibitors, NS5B RNA-dependent RNA polymerase inhibitors, NS5A inhibitors, and host-directed antivirals, such as cyclophilin inhibitors. Alternative interferons with possibly improved tolerability, specifically interferon-lambda 1 (interleukin-29), are also under development. These new reagents against hepatitis C virus should lead to highly effective, well-tolerated, and likely interferon-sparing therapies in the next several years.
引用
收藏
页码:1340 / +
页数:54
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