Antiviral Resistance and the Future Landscape of Hepatitis C Virus Infection Therapy

被引:74
|
作者
Wyles, David L. [1 ]
机构
[1] Univ Calif San Diego, Div Infect Dis, La Jolla, CA 92093 USA
来源
关键词
Hepatitis C; protease inhibitors; resistance; HCV GENOTYPE 1; HUMAN-IMMUNODEFICIENCY-VIRUS; DYNAMICS IN-VIVO; DRUG-RESISTANCE; VIRAL DYNAMICS; MUTATION-RATE; PROTEASE; TELAPREVIR; COMBINATION; PEGINTERFERON;
D O I
10.1093/infdis/jis761
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The addition of hepatitis C virus (HCV) protease inhibitors (PIs) to interferon and ribavirin therapy has significantly improved the efficacy of treatment for HCV infection. However, for patients who do not respond to therapy, the selection of HCV variants with resistance to PIs is likely. Resistant variants, such as R155K and A156T/V, result in extensive cross-resistance to other HCV PIs. Despite the rapid and frequent appearance of PI-resistant HCV variants, the long-term clinical implications are unknown. In particular, progress in the development of other HCV antivirals, such as NS5A inhibitors, next-generation NS3 protease inhibitors, and NS5B nucleoside and nonnucleoside inhibitors, has provided a broad selection of potent antivirals such that interferon-free therapy is a reality. Promising results from early stages of interferon-free trials will be reviewed.
引用
收藏
页码:S33 / S39
页数:7
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