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Modulation of TLR 3 7 and 8 Expressions in HCV Genotype 3 Infected Individuals: Potential Correlations of Pathogenesis and Spontaneous Clearance

机译:丙型肝炎病毒基因型3感染个体中TLR 37和8表达的调节:发病机制和自发清除的潜在相关性。

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摘要

Background. Hepatitis C virus is the major cause of chronic hepatitis worldwide which finally leads to the development of hepatocellular carcinoma. Toll like receptors (TLRs) play an important role in the course of many viral infections, but the role of TLRs in HCV pathogenesis has not been well elucidated so far. Objective. The aim of this study was to analyse the mRNA expression of TLRs 3, 7, and 8 in different stages of HCV infection including chronic, cirrhosis, interferon treated resolved, and relapsed cases. Methodology. Total RNA from whole blood was extracted and mRNA expression of TLRs 3, 7, and 8 genes was analyzed by quantitative real-time RT-PCR using β-Actin gene as an internal control. Results. This study consisted of 100 HCV infected individuals and twenty healthy controls. TLR 3 expression was found to be significantly elevated in individuals who had spontaneously cleared the virus (p < 0.001), whereas TLR 7 was found to be 3.26 times more elevated in patients with cirrhosis of liver. In IFN induced individuals, TLR 8 expression levels were found to be 2.28-fold elevated as compared to control population. Conclusion. TLRs 3, 7, and 8 are prime biomarker candidates for HCV infection mRNA expression analysis which might improve current therapeutic approaches.
机译:背景。丙型肝炎病毒是世界范围内慢性肝炎的主要原因,最终导致肝细胞癌的发展。类似Toll样受体(TLR)在许多病毒感染的过程中起着重要作用,但是到目前为止,TLR在HCV发病机理中的作用尚未得到很好的阐明。目的。这项研究的目的是分析HCV感染不同阶段(包括慢性,肝硬化,干扰素治疗的已治愈和复发病例)中TLR 3、7和8的mRNA表达。方法。从全血中提取总RNA,并使用β-Actin基因作为内部对照,通过定量实时RT-PCR分析TLR 3、7和8基因的mRNA表达。结果。这项研究由100位被HCV感染的个体和20位健康对照组成。发现自发清除病毒的个体中TLR 3的表达显着升高(p <0.001),而肝硬化患者中TLR 7的表达高3.26倍。在IFN诱导的个体中,发现TLR 8表达水平与对照人群相比升高了2.28倍。结论。 TLR 3、7和8是HCV感染mRNA表达分析的主要生物标志物候选物,可能会改善当前的治疗方法。

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