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基因编码巨噬细胞移动抑制因子的功能多态性与老年人革兰氏阴性菌血症有关。

Functional polymorphisms in the gene encoding macrophage migration inhibitory factor are associated with Gram-negative bacteremia in older adults.

机构信息

Department of Internal Medicine, University of Pennsylvania School of Medicine, Philadelphia.

出版信息

J Infect Dis. 2014 Mar 1;209(5):764-8. doi: 10.1093/infdis/jit571. Epub 2013 Oct 24.

Abstract

Macrophage migration inhibitory factor (MIF) is an immune mediator encoded in a functionally polymorphic locus. We found the genotype conferring low expression of MIF to be enriched in a cohort of 180 patients with gram-negative bacteremia, compared with 229 healthy controls (odds ratio [OR], 2.4; P = .04), an association that was more pronounced in older adults (OR, 4.6; P = .01). Among older subjects, those with low expression of MIF demonstrated 20% reduced MIF production from lipopolysaccharide-stimulated peripheral blood monocytes and 30% lower monocyte surface Toll-like receptor 4, compared with those with high expression. Our work suggests that older adults with low expression of MIF may be predisposed to hyporesponsiveness to lipopolysaccharide and gram-negative bacterial infection.

摘要

巨噬细胞移动抑制因子(MIF)是一种在功能上多态性的基因座编码的免疫介质。我们发现,与 229 名健康对照者相比,在 180 名革兰氏阴性菌血症患者的队列中,低表达 MIF 的基因型更为丰富(比值比 [OR],2.4;P =.04),这一关联在老年人中更为明显(OR,4.6;P =.01)。在老年人中,与高表达者相比,低表达 MIF 的个体从脂多糖刺激的外周血单核细胞中产生的 MIF 减少了 20%,单核细胞表面 Toll 样受体 4 减少了 30%。我们的工作表明,低表达 MIF 的老年人可能对脂多糖和革兰氏阴性细菌感染的反应性降低。

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