对结核分枝杆菌抗原免疫反应的定量关联试验:西非双胞胎的研究。

Amanda Wiart, Annette Jepson, Winston Banya, Steve Bennett, Hilton Whittle, Nicholas G Martin, Adrian V S Hill
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引用次数: 8

摘要

现在有相当多的证据表明,宿主遗传因素在决定结核分枝杆菌(MTB)感染的结果方面很重要。本研究的目的是评估几个候选基因在MTB抗原免疫反应中观察到的变异中的作用。体外检测t细胞增殖,体内皮内延迟超敏反应;在健康但暴露的西非双胞胎中评估了细胞因子和几种分枝杆菌肽抗原的抗体分泌。候选基因多态性在NRAMP1、维生素D受体、IL10、IL4、IL4受体和CTLA-4基因中分型。基因座il -10 (-1082 G/A)、CTLA-4 (49 A/G)和il -4受体(128 A/G)的变异与几种抗原的免疫应答显著相关。携带ctla - 4g等位基因的受试者的t细胞增殖反应和抗体反应降低,tnf - α反应增加。IL10基因型GA和GG的t细胞增殖反应差异显著。il - 4受体AG和GG基因型对MTB抗原的t细胞增殖反应也有显著差异。这些结果使人们对结核病免疫反应的遗传机制有了更深入的了解,并对治疗干预措施的设计产生了影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative association tests of immune responses to antigens of Mycobacterium tuberculosis: a study of twins in West Africa.
There is now considerable evidence that host genetic factors are important in determining the outcome of infection with Mycobacterium tuberculosis (MTB). The aim of this study was to assess the role of several candidate genes in the variation observed in the immune responses to MTB antigens. In-vitro assays of T-cell proliferation, an in-vivo intradermal delayed hypersensitivity response; cytokine and antibody secretions to several mycobacterial peptide antigens were assessed in healthy, but exposed, West African twins. Candidate gene polymorphisms were typed in the NRAMP1, Vitamin D receptor, IL10, IL4, IL4 receptor and CTLA-4 genes. Variants of the loci IL10 (-1082 G/A), CTLA-4 (49 A/G) and the IL4 receptor (128 A/G) showed significant associations with immune responses to several antigens. T-cell proliferative responses and antibody responses were reduced, TNF-alpha responses were increased for subjects with the CTLA-4 G allele. The T-cell proliferative responses of subjects with IL10 GA and GG genotypes differed significantly. IL4 receptor AG and GG genotypes also showed significant differences in their T-cell proliferative responses to MTB antigens. These results yield a greater understanding of the genetic mechanisms that underlie the immune responses in tuberculosis and have implications for the design of therapeutic interventions.
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