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印度人群中CCR5和SDF-1基因变异与HIV感染的分析。

Analysis of CCR5 and SDF-1 genetic variants and HIV infection in Indian population.

作者信息

Gupta A, Padh Harish

机构信息

Department of Cell and Molecular Biology, B.V. Patel Pharmaceutical Education and Research Development (PERD) Centre, Ahmedabad, Gujarat, India.

出版信息

Int J Immunogenet. 2015 Aug;42(4):270-8. doi: 10.1111/iji.12215. Epub 2015 Jun 21.

Abstract

HIV-1 infection and progression exhibits interindividual variation. The polymorphism in the chemokine receptors CCR5 and CXCR4, the principal coreceptors for HIV-1 and their ligands like SDF-1 have a profound effect in altering the HIV-1 disease progression rate. A single nucleotide polymorphism designated SDF1-3'UTR-801G-A has been associated with resistance to HIV-1 infection or delayed progression to AIDS. In this study, the SDF1-3'A polymorphism, CCR5∆32 polymorphism and CCR5 promoter polymorphism at positions 58934 G/T, 59029 G/A, 59353 T/C, 59356 C/T, 59402 A/G and 59653 C/T were analysed in Indian population. The polymorphisms in HIV-1 patients and healthy individuals were evaluated by conventional PCR, RFLP-PCR and direct sequencing techniques. The CCR5∆32 mutant allele was found to be almost absent in Indian population. The analysis of the CCR5-59356C/T polymorphism revealed a trend towards an association of the C allele with an increased risk of HIV-1 infection. The frequency of allele CCR5-59356C was higher in HIV-1 patients (100%) as compared to healthy control subjects (89%, P = 0.003). The correlation of SDF1-3'A and CCR5 promoter CCR5-58934G/T, CCR5-59029G/A, CCR5-59353T/C, CCR5-59402 A/G and CCR5-59653C/T polymorphisms and protection to HIV-1 infection and progression to AIDS was found to be nonsignificant. Nine haplotypes with more than 1% frequency were detected but were not significant in their protective role against HIV. Comparative analysis with global populations showed a noteworthy difference in CCR5 and SDF-1 polymorphisms' frequency distribution, indicating the ethnic variability of Indians. Although susceptibility to infections cannot be completely dependent on one or few genetic variants, it is important to remember that SDF-1 and CCR5 variants have been correlated globally with HIV-1 infection and disease progression. In the light of that, higher frequency of SDF-1 variants in the Indian population is noteworthy.

摘要

HIV-1感染及病情进展存在个体差异。趋化因子受体CCR5和CXCR4的多态性,作为HIV-1主要的共受体及其配体(如SDF-1),对改变HIV-1疾病进展速率具有深远影响。一种名为SDF1-3'UTR-801G-A的单核苷酸多态性与HIV-1感染抗性或延缓至艾滋病的进展相关。在本研究中,对印度人群中SDF1-3'A多态性、CCR5∆32多态性以及CCR5启动子在58934 G/T、59029 G/A、59353 T/C、59356 C/T、59402 A/G和59653 C/T位点的多态性进行了分析。通过常规PCR、RFLP-PCR和直接测序技术评估了HIV-1患者和健康个体中的多态性。发现CCR5∆32突变等位基因在印度人群中几乎不存在。对CCR5-59356C/T多态性的分析显示,C等位基因与HIV-1感染风险增加之间存在关联趋势。与健康对照受试者(89%,P = 0.003)相比,HIV-1患者中CCR5-59356C等位基因的频率更高(100%)。发现SDF1-3'A与CCR5启动子CCR5-58934G/T、CCR5-59029G/A、CCR5-59353T/C、CCR5-59402 A/G和CCR5-59653C/T多态性以及对HIV-1感染和进展至艾滋病的保护作用之间无显著相关性。检测到9种频率超过1%的单倍型,但它们对HIV的保护作用不显著。与全球人群的比较分析显示,CCR5和SDF-1多态性的频率分布存在显著差异,表明印度人群的种族变异性。尽管对感染易感性不能完全依赖于一个或少数几个基因变异,但重要的是要记住,SDF-1和CCR5变异在全球范围内都与HIV-1感染和疾病进展相关。鉴于此,印度人群中SDF-1变异的较高频率值得关注。

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