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干扰素-α和利巴韦林疗法对丙型肝炎病毒准种异质性的调节作用

Modulation of hepatitis C virus quasispecies heterogeneity by interferon-alpha and ribavirin therapy.

作者信息

González-Peralta R P, Liu W Z, Davis G L, Qian K P, Lau J Y

机构信息

Division of Gastroenterology and Hepatology, University of Florida, Gainesville 32610, USA.

出版信息

J Viral Hepat. 1997 Mar;4(2):99-106. doi: 10.1111/j.1365-2893.1997.tb00211.x.

Abstract

To determine the effects of interferon-alpha (IFN-alpha) and ribavirin therapy on hepatitis C virus (HCV) quasispecies heterogeneity, 29 patients with chronic HCV infection treated with either IFN-alpha (n = 15), ribavirin (n = 7) or placebo (n = 7) were studied. HCV quasispecies heterogeneity was determined by single-strand conformational polymorphism (SSCP) analysis of the HCV E2 hypervariable region 1 (HVR1). For patients receiving IFN-alpha, HVR1 was amplified in 14 of 15 patients before, and in six of seven patients after therapy. After controlling the amount of amplicon loaded, a reduction in the number of SSCP bands was observed with IFN-alpha therapy (median number of SSCP bands per patient was eight before therapy and two after therapy). In the seven patients within each of the ribavirin- and placebo-treated groups, there was no significant difference in the viraemia level, number of SSCP bands per patient or the SSCP band pattern, before and after therapy. These findings suggest that at the doses given, IFN-alpha, but not ribavirin, exerts a selective pressure on HCV quasispecies heterogeneity.

摘要

为确定干扰素-α(IFN-α)和利巴韦林治疗对丙型肝炎病毒(HCV)准种异质性的影响,我们研究了29例接受IFN-α(n = 15)、利巴韦林(n = 7)或安慰剂(n = 7)治疗的慢性HCV感染患者。通过对HCV E2高变区1(HVR1)进行单链构象多态性(SSCP)分析来确定HCV准种异质性。对于接受IFN-α治疗的患者,15例中有14例在治疗前扩增出HVR1,7例中有6例在治疗后扩增出HVR1。在控制扩增产物上样量后,观察到IFN-α治疗后SSCP条带数量减少(治疗前每位患者SSCP条带的中位数为8条,治疗后为2条)。在利巴韦林治疗组和安慰剂治疗组的每组7例患者中,治疗前后病毒血症水平、每位患者的SSCP条带数量或SSCP条带模式均无显著差异。这些发现表明,在给定剂量下,IFN-α而非利巴韦林对HCV准种异质性施加了选择性压力。

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