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首页> 外文期刊>Clinical and Experimental Immunology: An Official Journal of the British Society for Immunology >P2X7 and NRAMP1/SLC11 A1 gene polymorphisms in Mexican mestizo patients with pulmonary tuberculosis.
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P2X7 and NRAMP1/SLC11 A1 gene polymorphisms in Mexican mestizo patients with pulmonary tuberculosis.

机译:墨西哥患有肺结核的混血儿的P2X7和NRAMP1 / SLC11 A1基因多态性。

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Tuberculosis remains one of the most important infectious diseases worldwide. Several studies have suggested that genetic factors may affect susceptibility to tuberculosis, but the specific genes involved have not yet been fully characterized. NRAMP1/SLC11 A1 and P2X(7) genes have been linked to increased risk for tuberculosis in some African and Asiatic populations. To explore the potential role of these genes in the susceptibility to pulmonary tuberculosis in a Mexican mestizo population, we evaluated the association of D543N and 3'-UTR polymorphisms in NRAMP1/SLC11 A1 and - 762 and A1513C polymorphisms in P2X(7) genes with the risk for tuberculosis. Polymerase chain reaction (PCR) amplification of genomic DNA followed by restriction fragment length polymorphism analysis, and allelic-specific PCR was employed. We found no significant differences in allelic frequency in NRAMP1/SLC11 A1 gene polymorphisms in 94 patients with tuberculosis compared to 100 healthy contacts. Similarly, no significant association of the P2X(7)-762 gene polymorphism with tuberculosis was detected. In contrast, the P2X(7) A1513C polymorphism was associated significantly with tuberculosis (P = 0.02, odds ratio = 5.28, 95% CI, 0.99-37.69), an association that had not been reported previously. However, when the function of P2X(7) was assessed by an L-selectin loss assay, we did not find significant differences in patients compared to healthy contacts or between PPD(+) and PPD(-) control individuals. This study further supports the complex role of P2X(7) gene in host regulation of Mycobacterium tuberculosis infection, and demonstrates that different associations of gene polymorphisms and tuberculosis are found in distinct racial populations.
机译:结核病仍然是全世界最重要的传染病之一。几项研究表明,遗传因素可能会影响结核病的易感性,但是所涉及的特定基因尚未得到充分表征。 NRAMP1 / SLC11 A1和P2X(7)基因与某些非洲和亚洲人口患肺结核的风险增加有关。为了探索这些基因在墨西哥混血儿人群对肺结核易感性中的潜在作用,我们评估了NRAMP1 / SLC11 A1中D543N和3'-UTR多态与P2X(7)基因中-762和A1513C多态与结核病的风险。基因组DNA的聚合酶链反应(PCR)扩增,然后进行限制性片段长度多态性分析,并使用等位基因特异性PCR。我们发现与100名健康人相比,94名结核病患者的NRAMP1 / SLC11 A1基因多态性等位基因频率无显着差异。同样,没有检测到P2X(7)-762基因多态性与结核病有显着关联。相比之下,P2X(7)A1513C多态性与结核病显着相关(P = 0.02,优势比= 5.28,95%CI,0.99-37.69),这一关联以前未见报道。但是,当通过L-选择素损失测定法评估P2X(7)的功能时,与健康接触者或PPD(+)和PPD(-)对照个体相比,我们没有发现患者的显着差异。这项研究进一步支持P2X(7)基因在结核分枝杆菌感染宿主调控中的复杂作用,并证明在不同种族人群中发现了基因多态性与结核病的不同关联。

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