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首页> 外文期刊>International Journal of Hepatology >IFNL4 ss469415590 Variant Is Associated with Treatment Response in Japanese HCV Genotype 1 Infected Individuals Treated with IFN-Including Regimens
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IFNL4 ss469415590 Variant Is Associated with Treatment Response in Japanese HCV Genotype 1 Infected Individuals Treated with IFN-Including Regimens

机译:IFNL4 ss469415590变异体与日本HCV基因型1感染个体的治疗反应相关,包括IFN-γ的治疗

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Aim. Eradication of hepatitis C virus (HCV) is still challenging even if interferon- (IFN-) free regimens with direct-acting antiviral agents (DAAs) for HCV-infected individuals are available in clinical practice. IFNL4 is a newly described protein, associated with human antiviral defenses. We investigated whether IFNL4 ss469415590 variant has an effect on the prediction of treatment response in HCV-infected patients treated with IFN-including regimens.Patients and Methods. In all, 185 patients infected with HCV genotype 1 treated with peg-IFN plus ribavirin, with or without telaprevir, were genotyped for IFNL4 ss469415590. We retrospectively investigated whether the role of IFNL4 ss469415590 variant and other factors could predict sustained virological response (SVR) in Japanese patients infected with HCV genotype 1.Results. There were 65.7%, 31.5%, and 2.8% patients in the IFNL4 ss469415590 TT/TT, TT/-G, and -G/-G groups, respectively. SVR rates were 82.1% or 49.3% in patients treated with peg-IFN plus ribavirin with or without telaprevir, respectively. IFNL4 ss469415590 variant and HCV viral loads or IFNL4 ss469415590 variant and early virological response were better predictors of SVR in patients treated with peg-IFN plus ribavirin with or without telaprevir, respectively.Conclusion. In the era of DAAs, measurement of IFNL4 ss469415590 variant could help the prediction of SVR in Japanese HCV genotype 1 infected individuals treated with IFN-including regimens.
机译:目标。即使在临床实践中,即使有针对HCV感染者的直接作用抗病毒剂(DAA),无干扰素(IFN-)疗法也无法根除丙型肝炎病毒(HCV)。 IFNL4是一种新近描述的蛋白质,与人类抗病毒防御有关。我们调查了IFNL4 ss469415590变体是否对包括IFN方案在内的HCV感染患者的治疗反应预测产生影响。患者和方法。总共对185例接受peg-IFN加利巴韦林治疗的HCV基因1型感染的患者(无论是否使用telaprevir)进行IFNL4 ss469415590基因分型。我们回顾性调查了IFNL4 ss469415590变体的作用以及其他因素是否可以预测感染HCV基因型1的日本患者的持续病毒学应答(SVR)。 IFN / L4 ss469415590 TT / TT,TT / -G和-G / -G组分别有65.7%,31.5%和2.8%的患者。接受peg-IFN加利巴韦林联合或不联合telaprevir治疗的患者,SVR率分别为82.1%或49.3%。结论peg-IFN加利巴韦林联合或不联合telaprevir治疗的患者中,IFNL4 ss469415590变体和HCV病毒载量或IFNL4 ss469415590变体和早期病毒学应答是SVR的更好预测指标。在DAA时代,对IFNL4 ss469415590变异体的测量可以帮助预测日本HCV基因型1感染个体(包括IFN-方案)的SVR。

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