Søborg Christian, Andersen Aase Bengaard, Range Nyagosya, Malenganisho Wabyahe, Friis Henrik, Magnussen Pascal, Temu Mansuet M, Changalucha John, Madsen Hans O, Garred Peter
Tissue Typing Laboratory of the Department of Clinical Immunology, Rigshospitalet, Copenhagen, Denmark.
Mol Immunol. 2007 Mar;44(9):2213-20. doi: 10.1016/j.molimm.2006.11.002. Epub 2006 Dec 6.
Genetic susceptibility towards clinical tuberculosis has been proposed in several population studies. We investigated whether polymorphisms in the candidate genes encoding solute carrier 11a1 protein (SLC11A1 formerly NRAMP1), mannose-binding lectin (MBL2) and Vitamin D receptor (VDR) were associated with tuberculosis in an East-African setting. Four hundred and forty-three culture positive pulmonary tuberculosis patients and 426 controls from Mwanza district in the northern part of Tanzania were prospectively included. Polymorphisms in the candidate genes were detected by different PCR-based techniques. A significant association between pulmonary tuberculosis and a microsatellite marker in the 5'(CA)n locus in the SLC11A1 gene compared with controls (38% versus 30% odds ratio 1.45, 95% CI: 1.06-1.9, P=0.014) was observed. The association was apparent only in HIV negative tuberculosis patients. No association with tuberculosis was seen with 3 other SLC11A1 loci investigated, which previously have been associated with tuberculosis in other populations or with MBL2 and VDR polymorphisms. The tuberculosis associated microsatellite marker was situated on different SLC11A1 haplotypes. In this cohort a microsatellite marker in the 5'(CA)n locus situated in the SLC11A1 gene was associated with tuberculosis. The observed association was seen only in HIV negative patients suggesting that this genetic susceptibility for tuberculosis may be surpassed by co-infections.
多项人群研究提出了临床结核病的遗传易感性。我们调查了编码溶质载体11a1蛋白(SLC11A1,原称NRAMP1)、甘露糖结合凝集素(MBL2)和维生素D受体(VDR)的候选基因中的多态性是否与东非地区的结核病相关。前瞻性纳入了来自坦桑尼亚北部姆万扎地区的443例培养阳性的肺结核患者和426例对照。通过不同的基于PCR的技术检测候选基因中的多态性。与对照相比,观察到肺结核与SLC11A1基因5'(CA)n位点的微卫星标记之间存在显著关联(优势比1.45,95%可信区间:1.06 - 1.9,P = 0.014,分别为38%和30%)。该关联仅在HIV阴性的肺结核患者中明显。在所研究的其他3个SLC11A1位点以及MBL2和VDR多态性中,未发现与结核病的关联,这些位点先前在其他人群中与结核病相关。与结核病相关的微卫星标记位于不同的SLC11A1单倍型上。在该队列中,SLC11A1基因5'(CA)n位点的微卫星标记与结核病相关。观察到的关联仅在HIV阴性患者中出现,这表明这种结核病的遗传易感性可能会被合并感染所掩盖。