Understanding the hepatitis C virus life cycle paves the way for highly effective therapies

被引:430
作者
Scheel, Troels K. H. [1 ,2 ,3 ,4 ]
Rice, Charles M. [1 ]
机构
[1] Rockefeller Univ, Ctr Study Hepatitis C, Lab Virol & Infect Dis, New York, NY 10021 USA
[2] Copenhagen Univ Hosp, Copenhagen Hepatitis C Program, Dept Infect Dis, Hvidovre, Denmark
[3] Copenhagen Univ Hosp, Copenhagen Hepatitis C Program, Clin Res Ctr, Hvidovre, Denmark
[4] Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, Fac Hlth & Med Sci, Copenhagen, Denmark
基金
美国国家卫生研究院;
关键词
TREATMENT-NAIVE PATIENTS; SUSTAINED VIROLOGICAL RESPONSE; BROADLY NEUTRALIZING ANTIBODIES; HCV GENOTYPE 1; B TYPE-I; RNA REPLICATION; NS5A INHIBITOR; CRYSTAL-STRUCTURE; GLYCOPROTEIN E2; CORE PROTEIN;
D O I
10.1038/nm.3248
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
More than two decades of intense research has provided a detailed understanding of hepatitis C virus (HCV), which chronically infects 2% of the world's population. This effort has paved the way for the development of antiviral compounds to spare patients from life-threatening liver disease. An exciting new era in HCV therapy dawned with the recent approval of two viral protease inhibitors, used in combination with pegylated interferon-a and ribavirin; however, this is just the beginning. Multiple classes of antivirals with distinct targets promise highly efficient combinations, and interferon-free regimens with short treatment duration and fewer side effects are the future of HCV therapy. Ongoing and future trials will determine the best antiviral combinations and whether the current seemingly rich pipeline is sufficient for successful treatment of all patients in the face of major challenges, such as HCV diversity, viral resistance, the influence of host genetics, advanced liver disease and other co-morbidities.
引用
收藏
页码:837 / 849
页数:13
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