Toll-like receptors, tumor necrosis factor-α, and interleukin-10 gene polymorphisms in risk of pulmonary tuberculosis and disease severity

被引:57
作者
Ma, Mai-juan [1 ]
Xie, Lan-pin
Wu, Shu-cai
Tang, Fang [2 ]
Li, Hao [1 ]
Zhang, Zheng-shan [3 ]
Yang, Hong [1 ]
Chen, Su-li
Liu, Ning
Liu, Wei [1 ]
Cao, Wu-chun [1 ]
机构
[1] Beijing Inst Microbiol & Epidemiol, State Key Lab Pathogen & Biosecur, Beijing, Peoples R China
[2] Chinese Peoples Armed Police Forces, Ctr Dis Control & Prevent, Beijing, Peoples R China
[3] Chinese Peoples Liberat Army, 307 Hosp, Dept Neurosurg, Beijing, Peoples R China
关键词
Interleukin-10; Pulmonary tuberculosis; Single nucleotide polymorphisms; Toll like receptors; Tumor necrosis factor-alpha; INNATE IMMUNE-RESPONSE; MYCOBACTERIUM-TUBERCULOSIS; TNF-ALPHA; ARG753GLN POLYMORPHISM; HOST SUSCEPTIBILITY; CUTTING EDGE; INFECTION; IL-10; MICE; RECOGNITION;
D O I
10.1016/j.humimm.2010.07.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Toll-like receptors (TLRs) and cytokines play key roles in innate and adaptive immunity against Mycobacterium tuberculosis (M.TB). The aim of this study was to investigate whether the functional genetic variations at position 1805 G/T in TLR1, 2258 A/G in TLR2, -857 C/T, and -863 A/C in tumor necrosis factor-alpha (INF-alpha), as well as -819 C/T in interleukin-10 (IL-10) confer susceptibility to pulmonary tuberculosis (PTB). We performed a hospital-based case-control study using 543 case patients and 544 controls. Multivariate logistic regression analysis revealed that the TT genotype of -857 C/T in TNF-alpha gene was significantly associated with lower risk of PTB, in comparison with other genotypes (odds ratios [OR] = 0.68,95% confidence interval [CI] = 0.53-0.86, p = 0.001). Conversely, the genetic variants of 863 A/C in TNF-a gene was associated with susceptibility to PTB (OR = 2.42%, 95% CI = 1.28-4.59, p = 0.007) and clinical severity of disease (OR = 3.59%, 95% CI = 1.41-9.11, p = 0.007). Our results indicated that the variants in TNF-a gene were associated with susceptibility to PTB and clinical severity of disease, whereas no significance could be inferred from TLRs and IL-10 genes polymorphisms. Crown copyright (C) 2010 Published by Elsevier Inc. on behalf of American Society for Histocompatibility and Immunogenetics. All rights reserved.
引用
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页码:1005 / 1010
页数:6
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