Niño-Moreno P, Portales-Pérez D, Hernández-Castro B, Portales-Cervantes L, Flores-Meraz V, Baranda L, Gómez-Gómez A, Acuña-Alonzo V, Granados J, González-Amaro R
Dpto de Inmunología, Facultad de Medicina, Universidad Autónoma de San Luis Potosí, San Luis Potosí, México.
Clin Exp Immunol. 2007 Jun;148(3):469-77. doi: 10.1111/j.1365-2249.2007.03359.x.
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.
结核病仍然是全球最重要的传染病之一。多项研究表明,遗传因素可能影响对结核病的易感性,但所涉及的具体基因尚未完全明确。在一些非洲和亚洲人群中,NRAMP1/SLC11A1和P2X(7)基因与结核病风险增加有关。为了探究这些基因在墨西哥混血人群对肺结核易感性中的潜在作用,我们评估了NRAMP1/SLC11A1基因的D543N和3'-UTR多态性以及P2X(7)基因的-762和A1513C多态性与结核病风险的关联。采用聚合酶链反应(PCR)扩增基因组DNA,随后进行限制性片段长度多态性分析和等位基因特异性PCR。我们发现,与100名健康对照相比,94例结核病患者的NRAMP1/SLC11A1基因多态性等位基因频率无显著差异。同样,未检测到P2X(7)-762基因多态性与结核病有显著关联。相比之下,P2X(7) A1513C多态性与结核病显著相关(P = 0.02,优势比 = 5.28,95%可信区间,0.99 - 37.69),这一关联此前尚未见报道。然而,当通过L-选择素丢失试验评估P2X(7)的功能时,我们发现患者与健康对照之间或PPD(+)和PPD(-)对照个体之间没有显著差异。本研究进一步支持了P2X(7)基因在宿主对结核分枝杆菌感染调控中的复杂作用,并表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。