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DC-SIGN(CD209)、五聚素3和维生素D受体基因变异与西非人群患肺结核的风险相关。

DC-SIGN (CD209), pentraxin 3 and vitamin D receptor gene variants associate with pulmonary tuberculosis risk in West Africans.

作者信息

Olesen R, Wejse C, Velez D R, Bisseye C, Sodemann M, Aaby P, Rabna P, Worwui A, Chapman H, Diatta M, Adegbola R A, Hill P C, Østergaard L, Williams S M, Sirugo G

机构信息

MRC Laboratories, Banjul, The Gambia.

出版信息

Genes Immun. 2007 Sep;8(6):456-67. doi: 10.1038/sj.gene.6364410. Epub 2007 Jul 5.

Abstract

We investigated the role of DC-SIGN (CD209), long pentraxin 3 (PTX3) and vitamin D receptor (VDR) gene single nucleotide polymorphisms (SNPs) in susceptibility to pulmonary tuberculosis (TB) in 321 TB cases and 347 healthy controls from Guinea-Bissau. Five additional, functionally relevant SNPs within toll-like receptors (TLRs) 2, 4 and 9 were typed but found, when polymorphic, not to affect host vulnerability to pulmonary TB. We did not replicate an association between SNPs in the DC-SIGN promoter and TB. However, we found that two polymorphisms, one in DC-SIGN and one in VDR, were associated in a nonadditive model with disease risk when analyzed in combination with ethnicity (P=0.03 for DC-SIGN and P=0.003 for VDR). In addition, PTX3 haplotype frequencies significantly differed in cases compared to controls and a protective effect was found in association with a specific haplotype (OR 0.78, 95% CI 0.63-0.98). Our findings support previous data showing that VDR SNPs modulate the risk for TB in West Africans and suggest that variation within DC-SIGN and PTX3 also affect the disease outcome.

摘要

我们在来自几内亚比绍的321例肺结核(TB)病例和347名健康对照中,研究了树突状细胞特异性细胞间黏附分子-3抓取非整合素(DC-SIGN,即CD209)、长五聚体蛋白3(PTX3)和维生素D受体(VDR)基因单核苷酸多态性(SNP)在肺结核易感性中的作用。对Toll样受体(TLR)2、4和9内另外5个功能相关的SNP进行了分型,结果发现,这些SNP在呈多态性时并不影响宿主对肺结核的易感性。我们未能重复证实DC-SIGN启动子中的SNP与肺结核之间存在关联。然而,我们发现,当结合种族进行分析时,DC-SIGN中的一个多态性和VDR中的一个多态性在非加性模型中与疾病风险相关(DC-SIGN的P值为0.03,VDR的P值为0.003)。此外,与对照组相比,病例组中PTX3单倍型频率存在显著差异,并且发现一种特定单倍型具有保护作用(比值比0.78,95%置信区间0.63 - 0.98)。我们的研究结果支持了先前的数据,即VDR SNP可调节西非人群患肺结核的风险,并表明DC-SIGN和PTX3内的变异也会影响疾病结局。

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