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Strong Association of the rs4986790 Single Nucleotide Polymorphism (SNP) of the Toll-Like Receptor 4 (

机译:RS4986790的rs4986790单核苷酸多态性(SNP)的强烈关联(

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摘要

Human immunodeficiency virus (HIV) causes acquired immune deficiency syndrome (AIDS) and enters the host cell via CD4 and either CC-chemokine receptor 5 (CCR) or CXC-chemokine receptor 4 (CXCR4). HIV is directly recognized by toll-like receptor 4 (TLR4) and affects downstream immune-related signal pathways. In addition, stimulated TLR4 inhibits HIV-1 invasion, and the rs4986790 single nucleotide polymorphism (SNP) (D299G) of the TLR4 gene contributes to the risk of HIV-1 infection in an Indian population. To evaluate whether the rs4986790 SNP of the TLR4 gene is related to vulnerability to HIV-1 infection, we collected genetic information from HIV-1 patients in previous studies and performed an association analysis with a matched control population obtained from the 1000 Genomes Project. In addition, to strengthen the results of association analysis, we performed a meta-analysis. We identified a strong association between the rs4986791 SNP and susceptibility to HIV infection in HIV-infected patients in previous studies and a matched control population obtained from the 1000 Genomes Project. In addition, we found that the G allele of the rs4986791 SNP in the TLR4 gene is strongly related to susceptibility to HIV infection in three Caucasian populations (odd ratio = 2.29, 95% confidence interval: 1.72–3.07, p = 1.438 × 10−7) and all four populations (odd ratio = 2.22, 95% confidence interval: 1.74–2.84, p = 2 × 10−10) in a meta-analysis. To the best our knowledge, this was the first meta-analysis on the association between the rs4986791 SNP of the TLR4 gene and susceptibility to HIV infection.
机译:人的免疫缺陷病毒(HIV)导致获得的免疫缺乏症综合征(艾滋病),并通过CD4和CC-趋化因子受体5(CCR)或CXC-趋化因子受体4(CXCR4)进入宿主细胞。 HIV通过Toll样受体4(TLR4)直接识别,并影响下游免疫相关信号途径。此外,刺激的TLR4抑制HIV-1侵袭,TLR4基因的RS4986790单核苷酸多态性(SNP)(D299G)有助于印度人群中HIV-1感染的风险。为了评估TLR4基因的RS4986790 SNP是否与对HIV-1感染的脆弱性有关,我们从先前研究中收集了HIV-1患者的遗传信息,并进行了从1000个基因组项目获得的匹配控制群进行关联分析。此外,为了加强关联分析的结果,我们进行了荟萃分析。我们在先前研究中艾滋病毒感染患者的RS4986791 SNP和艾滋病毒感染的敏感性和敏感性的强烈关联,以及从1000个基因组项目获得的匹配控制群。此外,我们发现TLR4基因的RS4986791 SNP的G等位基因与三种高加索人群(奇数比率= 2.29,95%置信区间:1.72-3.07,P = 1.438×10-)对HIV感染的易感性强烈有关。 7)和所有四个群体(奇数比率= 2.22,95%置信区间:1.74-2.84,P = 2×10-10)在META分析中。据我们所知,这是第一次关于TLR4基因的RS4986791 SNP与艾滋病毒感染易感性之间的关联的第一个荟萃分析。

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