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印度孟买围产期HIV传播中促炎细胞因子TNF-α启动子区域的基因变异

Genetic variation in the promoter region of pro-inflammatory cytokine TNF-α in perinatal HIV transmission from Mumbai, India.

作者信息

Ahir Swati, Mania-Pramanik Jayanti, Chavan Vijay, Kerkar Shilpa, Samant-Mavani Padmaja, Nanavati Ruchi, Mehta Preeti

机构信息

Department of Infectious Diseases Biology, National Institute for Research in Reproductive Health (DHR/ICMR), J.M. Street, Parel, Mumbai 400 012, Maharashtra, India.

Department of Infectious Diseases Biology, National Institute for Research in Reproductive Health (DHR/ICMR), J.M. Street, Parel, Mumbai 400 012, Maharashtra, India.

出版信息

Cytokine. 2015 Mar;72(1):25-30. doi: 10.1016/j.cyto.2014.11.022. Epub 2014 Dec 24.

Abstract

Various host factors such as cytokines and HLA, regulate the immune system and influence HIV transmission to infants exposed to HIV-1 through their mothers. Tumor Necrosis Factor Alpha (TNF-α) is a strong pro-inflammatory mediator and thought to influence vulnerability to HIV infection (and/or) transmission. Polymorphisms in regulatory regions are known to govern the production of this cytokine. However, the association of these variations in perinatal HIV transmission is yet to be established. Present study aimed to evaluate if polymorphisms in promoter region of TNF-α gene is associated with perinatal HIV transmission. With informed consent from parents, infants' blood was collected for HIV screening and SNPs analysis at 2 loci: TNF (rs1800629) and TNF (rs361525) using PCR-SSP method. HIV positive (n = 27) and negative (n = 54) children at the end of 18th month follow up were considered for this study. GG genotype, responsible for low expression of TNF (rs1800629) was significantly (p = 0.005) higher in uninfected children, while higher GA genotype frequency was observed in infected children. The 'G' allele frequency was significantly higher in negative children (p = 0.016). We conclude that genotypic variants of TNF (rs1800629) are a likely contributor to perinatal HIV transmission. This provides new insights in markers of differential susceptibility to perinatal HIV transmission.

摘要

多种宿主因素,如细胞因子和人类白细胞抗原(HLA),调节免疫系统并影响通过母亲接触HIV-1的婴儿感染HIV。肿瘤坏死因子α(TNF-α)是一种强大的促炎介质,被认为会影响HIV感染(和/或)传播的易感性。已知调节区域的多态性控制这种细胞因子的产生。然而,这些变异与围产期HIV传播之间的关联尚未确立。本研究旨在评估TNF-α基因启动子区域的多态性是否与围产期HIV传播相关。在获得父母知情同意后,采集婴儿血液,采用聚合酶链反应-序列特异性引物(PCR-SSP)方法对2个位点:TNF(rs1800629)和TNF(rs361525)进行HIV筛查和单核苷酸多态性(SNP)分析。本研究纳入了18个月随访结束时HIV阳性(n = 27)和阴性(n = 54)的儿童。导致TNF(rs1800629)低表达的GG基因型在未感染儿童中显著更高(p = 0.005),而在感染儿童中观察到更高的GA基因型频率。“G”等位基因频率在阴性儿童中显著更高(p = 0.016)。我们得出结论,TNF(rs1800629)的基因变异可能是围产期HIV传播的一个因素。这为围产期HIV传播易感性差异的标志物提供了新的见解。

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