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Correlation between polymorphisms in toll-like receptor genes and the activity of hepatitis B virus among treatment-na?ve patients: a case-control study in a Han Chinese population

机译:治疗 - 钠患者肝炎病毒多态性多态性与乙型肝炎病毒的相关性:汉族人群中病例对照研究

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Because of the high prevalence and absence of cure for infection, chronic hepatitis B virus (HBV) infection has been acknowledged as a pressing public health issue. Toll-like receptors (TLRs) activate the human innate immune system and the polymorphisms in TLRs may alter their function. The present study aimed to investigate the association between TLR polymorphisms and disease progression of chronic HBV infection. During the study period, 211 treatment-na?ve patients with chronic HBV infection were recruited, and blood samples were collected from each individual. Matrix-assisted laser desorption/ionization time of flight mass spectrometry was employed to genotype the selected TLR polymorphisms after human genome extraction. In addition, HbsAg, TNF-α, and IL-6 levels were quantified using enzyme linked immunosorbent assay (ELISA). Statistical analyses were conducted to investigate the association between TLR polymorphisms and hepatitis activity, liver function parameters, HbsAg level, and cytokine level. We did not observe any mutations in rs4986790, rs4986791, and rs5743708 among all study subjects. A logistic regression revealed that mutations in rs3804099 and rs4696480 were associated with milder hepatitis activity. Consistent with the logistic regression, improved liver function parameters and reduced level of both HbsAg and cytokines were also correlated with the mutant carriers of rs3804099 and rs4696480. TLR mutations were significantly associated with milder hepatitis activity among patients with chronic HBV infection. Therefore, we conclude that the activation of TLR pathways may further intensify the inflammation of hepatocytes, and leads to progression of disease.
机译:由于感染的患病率高和治愈的缺乏,慢性乙型肝炎病毒(HBV)感染被认为是一个紧迫的公共卫生问题。 Toll样受体(TLRS)激活人体先天免疫系统,TLR中的多态性可能会改变它们的功能。本研究旨在探讨TLR多态性与慢性HBV感染疾病进展的关联。在研究期间,募集了211例治疗 - Na'VE患者慢性HBV感染患者,从每个人收集血液样品。基质辅助激光解吸/电离飞行质谱时间以在人类基因组提取后基因型选择的TLR多态性进行基因型。此外,使用酶联免疫吸附测定(ELISA)量化HbsAg,TNF-α和IL-6水平。进行统计分析以研究TLR多态性和肝炎活动,肝功能参数,HBsAg水平和细胞因子水平之间的关联。我们在所有研究科目中没有观察到RS4986790,RS4986791和RS5743708中的任何突变。逻辑回归揭示了RS3804099和RS4696480中的突变与肝炎肝炎活动有关。与逻辑回归一致,改善肝功能参数和HBsAg和细胞因子的降低水平也与RS3804099和RS4696480的突变载体相关。 TLR突变与慢性HBV感染患者的肝炎活动显着相关。因此,我们得出结论,TLR途径的激活可以进一步加剧肝细胞的炎症,并导致疾病的进展。

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