Association of IL28B genotype and viral response of hepatitis C virus genotype 2 to interferon plus ribavirin combination therapy

被引:7
作者
Akuta, Norio [1 ]
Suzuki, Fumitaka
Seko, Yuya
Kawamura, Yusuke
Sezaki, Hitomi
Suzuki, Yoshiyuki
Hosaka, Tetsuya
Kobayashi, Masahiro
Kobayashi, Mariko [2 ]
Saitoh, Satoshi
Arase, Yasuji
Ikeda, Kenji
Kumada, Hiromitsu
机构
[1] Toranomon Gen Hosp, Dept Hepatol, Okinaka Mem Inst Med Res, Minato Ku, Tokyo 1050001, Japan
[2] Toranomon Gen Hosp, Liver Res Lab, Tokyo 1050001, Japan
关键词
HCV; IL28B; genotype; 2; interferon; ribavirin; sustained virological response; GENOME-WIDE ASSOCIATION; SUSTAINED VIROLOGICAL RESPONSE; PEGINTERFERON ALPHA-2B; GENETIC-VARIATION; CORE REGION; HCV-RNA; INFECTION; TELAPREVIR; EFFICACY; PERIOD;
D O I
10.1002/jmv.23368
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The impacts of IL28B genotype to treatment response of hepatitis C virus (HCV) genotype 2 are still not clear. A total of 381 consecutive Japanese patients infected with HCV genotype 2, who could complete combination therapy with interferon (IFN) plus ribavirin for 24 weeks, were evaluated to investigate pretreatment predictors. Patients, who could not achieve sustained virological response at the first course of 24-week IFN plus ribavirin, were recruited into the study protocol of total 48-week IFN plus ribavirin. In 24-week regimen, rates of sustained virological response and rapid virological response were 82% and 50%, respectively. There were no significant differences in rates of sustained virological response and rapid virological response, according to IL28B genotype. Multivariate analysis identified younger age, higher level of albumin, absence of past history of IFN, and lower level of viremia as significant determinants of sustained virological response. As significant or marginal significant determinants of non-sustained virological response regardless of rapid virological response, multivariate analysis identified IL28B rs8099917 genotype TG?+?GG and lower level of albumin. In 48-week regimen to 10 patients of non-sustained virological response at the first course of 24-week regimen, sustained virological response rates were 70%. All of six patients, with IL28B TT and relapse at the first course of 24-week regimen, could achieve sustained virological response, but two patients with IL28B TG could not achieve sustained virological response. In conclusion, the present results suggest that IL28B genotype might partly affect viral response of HCV genotype 2 to combination therapy. J. Med. Virol. 84:15931599, 2012. (c) 2012 Wiley Periodicals, Inc.
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页码:1593 / 1599
页数:7
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