首页> 外文期刊>Journal of clinical virology: The official publication of the Pan American Society for Clinical Virology >Dynamics of serum hepatitis C virus load and quasispecies complexity during antiviral therapy in patients with chronic hepatitis C.
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Dynamics of serum hepatitis C virus load and quasispecies complexity during antiviral therapy in patients with chronic hepatitis C.

机译:慢性丙型肝炎患者抗病毒治疗期间血清丙型肝炎病毒载量和准种复杂性的动态。

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BACKGROUND: Hepatitis C virus (HCV) infection is a dynamic process during which viral genetic variants continuously develop as a result of the virus adaptation to the host's immune system. The level of viremia and the complexity of the hypervariable region 1 (HVR 1) quasispecies of hepatitis C virus during antiviral therapy reflect the dynamic balance between the viral and host components in response to therapy. OBJECTIVE: The aim of the study was to evaluate the dynamics of HCV viremia and the complexity of the HVR 1 quasispecies during the induction phase of a triple combination therapy regimen in nonresponders to earlier anti-HCV treatment. STUDY DESIGN: Ten patients with chronic hepatitis C undergoing antiviral combination therapy with interferon-alpha, ribavirin, and amantadine were studied. The serum HCV RNA level was monitored by a quantitative RT-PCR assay up to 3 months after start of treatment. The HVR 1 quasispecies complexity was analysed by an "in house" nested RT-PCR mediated single-strand conformation polymorphism (SSCP) assay. RESULTS: Baseline serum HCV RNA levels ranged from 1.94x10(6) to 5.53x10(6) copies/ml. In all patients, HCV subtype 1b was found. At the start of therapy, the SSCP assay revealed a high complexity pattern (at least six SSCP bands) in all patients. None of the patients responded within 4 weeks of treatment, however, the serum HCV RNA level decreased by one to two logs in eight patients. At week 4 after start of treatment, there was a decrease of SSCP bands in five patients. In four patients, SSCP bands remained unchanged and in one patient SSCP bands increased. At month 3 after start of treatment, serum HCV RNA was not detectable in one patient. CONCLUSION: Because of the low number of patients involved in this study, prediction of therapeutical success based on the quasispecies complexity was not possible. Larger studies are urgently needed.
机译:背景:丙型肝炎病毒(HCV)感染是一个动态过程,在此过程中,由于病毒适应宿主的免疫系统,病毒遗传变异不断发展。抗病毒治疗期间丙型肝炎病毒的病毒血症水平和高变区1(HVR 1)准种的复杂性反映了治疗对病毒和宿主成分之间的动态平衡。目的:本研究旨在评估在对早期抗HCV治疗无反应的三联疗法中,HCV病毒血症的动态变化和HVR 1准种的复杂性。研究设计:研究了十名慢性丙型肝炎患者,他们接受了干扰素-α,利巴韦林和金刚烷胺的抗病毒联合治疗。在治疗开始后的3个月内,通过定量RT-PCR测定法监测血清HCV RNA水平。通过“内部”嵌套RT-PCR介导的单链构象多态性(SSCP)分析来分析HVR 1准种的复杂性。结果:基线血清HCV RNA水平范围从1.94x10(6)到5.53x10(6)拷贝/ ml。在所有患者中,均发现了HCV 1b亚型。在治疗开始时,SSCP分析在所有患者中均显示出高复杂性模式(至少六个SSCP谱带)。在治疗的4周内没有患者反应,但是8例患者的血清HCV RNA水平下降了1至2个对数。开始治疗后第4周,有5例患者的SSCP条带减少。在四名患者中,SSCP谱带保持不变,而在一名患者中,SSCP谱带增加。治疗开始后第3个月,一名患者未检测到血清HCV RNA。结论:由于参与本研究的患者人数很少,因此不可能基于准种的复杂性预测治疗成功。迫切需要更大的研究。

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