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Linkage and association analysis of candidate genes for TB and TNFalpha cytokine expression: evidence for association with IFNGR1, IL-10, and TNF receptor 1 genes.

机译:TB和TNFalpha细胞因子表达候选基因的关联和关联分析:与IFNGR1,IL-10和TNF受体1基因关联的证据。

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Tuberculosis (TB) is a growing public health threat globally and several studies suggest a role of host genetic susceptibility in increased TB risk. As part of a household contact study in Kampala, Uganda, we have taken a unique approach to the study of genetic susceptibility to TB by developing an intermediate phenotype model for TB susceptibility, analyzing levels of tumor necrosis factor-alpha (TNFalpha) in response to culture filtrate as the phenotype. In the present study, we analyzed candidate genes related to TNFalpha regulation and found that interleukin (IL)-10, interferon-gamma receptor 1 (IFNGR1), and TNFalpha receptor 1 (TNFR1) genes were linked and associated to both TB and TNFalpha. We also show that these associations are with progression to active disease and not susceptibility to latent infection. This is the first report of an association between TB and TNFR1 in a human population and our findings for IL-10 and IFNGR1 replicate previous findings. By observing pleiotropic effects on both phenotypes, we show construct validity of our intermediate phenotype model, which enables the characterization of the role of these genetic polymorphisms on TB pathogenesis. This study further illustrates the utility of such a model for disentangling complex traits.
机译:结核病(TB)是全球范围内日益严重的公共卫生威胁,一些研究表明宿主遗传易感性在结核病风险增加中的作用。作为在乌干达坎帕拉进行的家庭接触研究的一部分,我们采用了独特的方法来研究结核病的遗传易感性,方法是建立结核病易感性的中间表型模型,分析肿瘤坏死因子-α(TNFalpha)的水平以应对结核病。培养滤液为表型。在本研究中,我们分析了与TNFalpha调控相关的候选基因,发现白介素(IL)-10,干扰素-γ受体1(IFNGR1)和TNFalpha受体1(TNFR1)基因相互关联并与TB和TNFalpha相关。我们还表明,这些关联与活动性疾病的进展有关,而与潜在感染无关。这是人类人群中TB与TNFR1之间相关性的第一份报告,我们对IL-10和IFNGR1的发现重复了先前的发现。通过观察对两种表型的多效性作用,我们表明了我们的中间表型模型的构建有效性,这使得能够表征这些遗传多态性在结核病发病机制中的作用。这项研究进一步说明了这种模型用于解开复杂特征的实用性。

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