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Is the use of IL28B genotype justified in the era of interferon-free treatments for hepatitis C?

机译:在丙型肝炎的无干扰素治疗时代使用IL28B基因型是否合理?

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摘要

In 2009, several groups reported that interleukin-28B (IL28B) genotypes are associated with the response to peginterferon plus ribavirin therapy for chronic hepatitis C virus (HCV) infection in a genome-wide association study, although the mechanism of this association is not yet well understood. However, in recent years, tremendous progress has been made in the treatment of HCV infection. In Japan, some patients infected with HCV have the IL28B major genotype, which may indicate a favorable response to interferon-including regimens; however, certain patients within this group are also interferon-intolerant or ineligible. In Japan, interferon-free 24-wk regimens of asunaprevir and daclatasvir are now available for HCV genotype 1b-infected patients who are interferon-intolerant or ineligible or previous treatment null-responders. The treatment response to interferon-free regimens appears better, regardless of IL28B genotype. Maybe other interferon-free regimens will widely be available soon. In conclusion, although some HCV-infected individuals have IL28B favorable alleles, importance of IL28B will be reduced with availability of oral interferon free regimen.
机译:在2009年,一些研究小组报告说,在全基因组关联研究中,白介素28B(IL28B)基因型与对聚乙二醇干扰素联合利巴韦林治疗慢性丙型肝炎病毒(HCV)感染的反应相关,尽管这种关联的机制尚未确定非常明白。然而,近年来,在HCV感染的治疗中已经取得了巨大的进步。在日本,一些感染HCV的患者具有IL28B主要基因型,这可能表明对包括干扰素在内的治疗方案有良好的反应。但是,该组中的某些患者也不能耐受干扰素或不符合要求。在日本,现在可以将无干扰素的Asunaprevir和daclatasvir的24周疗程用于感染HCV基因型1b的患者,这些患者不能接受干扰素或不能接受干扰素治疗,或者以前曾接受过无效治疗。不论IL28B基因型如何,对无干扰素方案的治疗反应似乎都更好。也许其他的无干扰素治疗方案很快就会广泛使用。总之,尽管某些HCV感染的个体具有IL28B有利的等位基因,但随着口服无干扰素治疗方案的普及,IL28B的重要性将降低。

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