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首页> 外文期刊>Journal of Infectious Diseases >Impact of a Functional KIR2DS4 Allele on Heterosexual HIV-1 Transmission among Discordant Zambian Couples
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Impact of a Functional KIR2DS4 Allele on Heterosexual HIV-1 Transmission among Discordant Zambian Couples

机译:功能性KIR2DS4等位基因对不一致的赞比亚夫妇间异性HIV-1传播的影响

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摘要

Killer cell immunoglobulin-like receptors (KIRs) and their HLA ligands interact to regulate natural killer (NK) cell function. KIR gene content and allelic variations are reported to influence human immunodeficiency virus (HIV)-1 infection and pathogenesis. We investigated the impact of KIR genes on heterosexual HIV-1 transmission among 566 discordant couples from Lusaka, Zambia. KIR2DS4*001, the only allele of KIR2DS4 known to encode a functional activating receptor, was associated with relatively high viral load for HIV-1 in index (HIV-1 seroprevalent) partners (β [standard error (SE)], .17 [.8] log10; P = .04) and with accelerated transmission of HIV-1 to cohabiting seronegative partners (relative hazard [RH], 2.00; P = .004). The latter association was independent of the direction of transmission (male-to-female or female-to-male), genital ulcers, and carriage of the putative ligand (HLA-Cw*04). No KIR-gene variant in the initially seronegative partners was associated with HIV-1 acquisition or early viral load following seroconversion. Further analysis of NK cell function should clarify the role of KIR2DS4*001 in HIV-1 transmission.
机译:杀伤细胞免疫球蛋白样受体(KIR)及其HLA配体相互作用,调节自然杀伤(NK)细胞功能。据报道,KIR基因含量和等位基因变异会影响人类免疫缺陷病毒(HIV)-1感染和发病机理。我们调查了KIR基因对来自赞比亚卢萨卡的566对不和谐夫妇中异性HIV-1传播的影响。 KIR2DS4 * 001是KIR2DS4已知编码功能激活受体的唯一等位基因,与HIV-1血清中相对较高的HIV-1病毒载量相关(指数[HIV-1血清亚型]伴侣)(β[标准误差(SE)] ,. 17 [ .8] log 10 ; P = .04),并且HIV-1加速传播给同居的血清阴性伴侣(相对危险[RH],2.00; P = .004)。后者的关联与传播方向(男性对女性或女性对男性),生殖器溃疡和推定配体的运输(HLA-Cw * 04)无关。在最初的血清反应阴性伴侣中,没有KIR基因变异与血清转化后的HIV-1获取或早期病毒载量有关。 NK细胞功能的进一步分析应阐明KIR2DS4 * 001在HIV-1传播中的作用。

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  • 来源
    《Journal of Infectious Diseases》 |2011年第4期|p.487-495|共9页
  • 作者单位

    Department of Medicine|Department of Microbiology;

    Department of Epidemiology, University of Alabama at Birmingham, Birmingham, Alabama;

    Department of Epidemiology, University of Alabama at Birmingham, Birmingham, Alabama;

    Rwanda-Zambia HIV-1 Research Group, Lusaka, Zambia;

    Rwanda-Zambia HIV-1 Research Group, Lusaka, Zambia|Department of Pathology and Laboratory Medicine;

    Vaccine Research Center, Emory University, Atlanta, Georgia;

    Department of Medicine|Department of Microbiology;

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