Macrophage migration inhibitory factor gene influences the risk of developing tuberculosis in northwestern Colombian population

被引:34
作者
Gomez, L. M.
Sanchez, E.
Ruiz-Narvaez, E. A.
Lopez-Nevot, M. A.
Anaya, J.-M.
Martin, J.
机构
[1] CIB, Cellular Biol & Immunogenet Unit, Medellin, Colombia
[2] CSIC, Inst Parasitol & Biomed Lopez Neyra, Granada, Spain
[3] Harvard Sch Publ Hlth, Dept Nutr, Boston, MA USA
[4] Harvard Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[5] Hosp Virgen Nieves, Serv Inmunol, Granada, Spain
[6] Univ Rosario, Sch Med, Medellin, Colombia
来源
TISSUE ANTIGENS | 2007年 / 70卷 / 01期
关键词
delayed-type hypersensitivity; microsatellite; MIF; polymorphism; single nucleotide; tuberculin skin test; tuberculosis;
D O I
10.1111/j.1399-0039.2007.00843.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Macrophage migration inhibitory factor (MIF) is a pleiotropic cytokine that regulates innate and adaptative immunity responses against pathogens. The MIF gene, at 22q11.2, is polymorphic. Functional promoter variants in the MIF gene influence susceptibility to inflammatory diseases in Caucasians and Africans. An association study was carried out to examine the influence of MIF-173 single nucleotide polymorphism and the MIF-794 microsatellite on the susceptibility to develop human tuberculosis (TB) in a well-defined Latin-American population. To this purpose, 230 northwestern Colombian patients with pulmonary TB, negative for human immunodeficiency virus infection, and 235 matched healthy individuals stratified by the tuberculin skin test were examined. Multivariate analysis showed that MIF-173C allele was associated with disease (odds ratio = 1.64, 95% confidence interval 1.07-2.52) in a dominant pattern. No allele in the MIF-794 CATT microsatellite was associated with risk of TB. These results indicate that MIF gene influences the risk of developing TB in the studied population.
引用
收藏
页码:28 / 33
页数:6
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