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Association study of polymorphisms in interferon-gamma receptor genes with the risk of pulmonary tuberculosis

机译:干扰素-γ受体基因多态性与肺结核风险的相关性研究

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Tuberculosis (TB) is an infectious disease caused by mycobacterium, which most commonly affects the lungs. The adaptive immune response in Mycobacterium tuberculosis is predominantly mediated by the interferon- (IFN-) signaling pathway, which is regulated by IFN- receptors (IFNGR). IFN- activates the transcription of a number of genes that are important in immune responses, thus the appropriate function of IFNGR appears to be important in host defense against mycobacteria. In the present study, 22 genetic variants in IFNGR1 and IFNGR2 were genotyped in 673 patients and 592 normal controls to investigate the association between IFNGR1 and IFNGR2 polymorphisms and the risk of TB. Statistical analyses revealed that four genetic variants in IFNGR1, rs9376269, rs9376268, rs9376267 and rs56251346 were marginally associated with the risk of TB (P=0.02-0.04), while other single nucleotide polymorphisms in IFNGR1 and IFNGR2 did not exhibit any associations. However, the significance of the four genetic variants rs9376269, rs9376268, rs9376267 and rs56251346 was eliminated following a multiple testing correction of the data (P>0.05). The present results revealed that certain genetic variants in IFNGR genes may be associated with TB development, which may be useful preliminary data for future investigation.
机译:结核病(TB)是一种由分枝杆菌引起的感染性疾病,最常见于肺部。结核分枝杆菌中的适应性免疫反应主要由干扰素(IFN-)信号通路介导,该信号通路由IFN-受体(IFNGR)调节。 IFN-激活许多在免疫反应中重要的基因的转录,因此IFNGR的适当功能似乎在宿主抵抗分枝杆菌的防御中很重要。在本研究中,对673名患者和592名正常对照中IFNGR1和IFNGR2的22个遗传变异进行了基因分型,以研究IFNGR1和IFNGR2多态性与结核病风险之间的关系。统计分析显示,IFNGR1,rs9376269,rs9376268,rs9376267和rs56251346中的四个遗传变异与TB的风险相关(P = 0.02-0.04),而IFNGR1和IFNGR2中的其他单核苷酸多态性没有任何关联。但是,经过多次测试校正后,消除了四个遗传变异体rs9376269,rs9376268,rs9376267和rs56251346的重要性(P> 0.05)。目前的结果表明,IFNGR基因中的某些遗传变异可能与结核病的发展有关,这可能对将来的研究有用。

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