首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Analysis of Mutations within the 5′ Untranslated Region Interferon Sensitivity Region and PePHD Region as a Function of Response to Interferon Therapy in Hepatitis C Virus-Infected Patients in India
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Analysis of Mutations within the 5′ Untranslated Region Interferon Sensitivity Region and PePHD Region as a Function of Response to Interferon Therapy in Hepatitis C Virus-Infected Patients in India

机译:印度丙型肝炎病毒感染患者对5非翻译区干扰素敏感区和PePHD区域内突变的影响分析其对干扰素治疗的反应

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摘要

Mutations in several subgenomic regions have been implicated in influencing response to interferon therapy; however, a comprehensive picture of Indian patients was lacking. Based on the viral load and clinical factors, 10 out of 15 patients were found to be complete responders, whereas 5 patients were nonresponders. The pretreatment viral RNA load of the patients was found to be between 5.20 and 6.13 log10 IU/ml, which eventually fell to 2.77 log10 IU/ml after 24 weeks of treatment, whereas in the case of nonresponders, the average was 5.38 log10 IU/ml. In order to study the influence of the hepatitis C virus genotype on the response to interferon therapy, the 5′ untranslated region sequences of the samples were analyzed, which showed that genotype 3 patients responded better than genotype 1 patients. Additionally, the mutations in the interferon sensitivity-determining region (ISDR) of the NS5A protein and the double-stranded RNA-activated protein kinase-eukaryotic initiation factor 2 alpha phosphorylation homology domain (PePHD) of the E2 envelope protein, before and after treatment, were compared with nonresponder prototype J. Although, no clear correlation was found in the case of the mutated ISDR, some significant changes in residues were observed in the PePHD region, which could be helpful in understanding the molecular basis of resistance to therapy. Interestingly, analysis of the quasispecies variations showed a change in genotype in one sample during treatment, which might have contributed to the resistance. The results suggest that the mutations in different regions of the viral genome might have a concerted effect on the response to interferon therapy.
机译:几个亚基因组区域的突变与影响对干扰素治疗的反应有关。但是,缺乏对印度患者的全面了解。根据病毒载量和临床因素,发现15名患者中有10名是完全缓解者,而5名患者是无缓解者。患者的治疗前病毒RNA载量在5.20至6.13 log10 IU / ml之间,在治疗24周后最终降至2.77 log10 IU / ml,而在无反应者中,平均值为5.38 log10 IU / ml。毫升为了研究丙型肝炎病毒基因型对干扰素治疗反应的影响,分析了样本的5'非翻译区序列,结果表明基因型3患者的反应优于基因型1患者。此外,治疗前后NS5A蛋白的干扰素敏感性决定区(ISDR)和E2包膜蛋白的双链RNA激活蛋白激酶-真核起始因子2α磷酸化同源结构域(PePHD)中的突变,与无应答原型J进行了比较。尽管在ISDR突变的情况下未发现明显的相关性,但在PePHD区域观察到一些残基的显着变化,这可能有助于理解抗药性的分子基础。有趣的是,对准种变异的分析表明,在处理过程中一个样品的基因型发生了变化,这可能是导致耐药性的原因。结果表明,病毒基因组不同区域的突变可能对干扰素治疗产生协同作用。

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