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γ-干扰素基因多态性与布鲁氏菌病感染易感性的关系。

Relationship between γ-interferon gene polymorphisms and susceptibility to brucellosis infection.

机构信息

Cellular and Molecular Research Center; Department of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Khalije Fars Boulevarde, Zahedan 14155‐6455,.

出版信息

Microbiol Immunol. 2013 Nov;57(11):785-91. doi: 10.1111/1348-0421.12093.

DOI:10.1111/1348-0421.12093
PMID:24033468
Abstract

Interferon-gamma (IFN-γ) is a pro-inflammatory cytokine that plays a pivotal role in the defense mechanism against Brucella infection. It was hypothesized that the IFN-γ in (+874 A/T in intron 1) TT and +5644 T/A, TT genotypes, which are reportedly associated with high IFN production, are associated with susceptibility to brucellosis in Iranian subjects. Genotyping of these IFN-γ variants by an allele-specific polymerase chain reaction method was performed in 281 subjects, comprising 153 patients with active brucellosis and 128 healthy controls. It was found that the +874 minor allele (A) and homozygote genotype (AA) were significantly more frequently present in brucellosis patients than in controls (OR = 2.588; 95% CI, 1.313-5.104; P = 0.006 for the AA genotype; OR = 1.575; 95% CI, 1.124-2.216; P = 0.010 for the A allele). However, the allelic and genotypic distribution of the IFN-γ polymorphism at position UTR5644 A>T did not differ significantly between patients and controls (P > 0.05). The distribution of haplotypes in this study suggests that the T/A haplotype (+874/UTR5644), which was present more frequently in controls than in patients, may protect subjects against Brucella infection. It is suggested that IFN-γ +874 AA genotype and A allele are risk factors for developing brucellosis infection in Iranian subjects.

摘要

干扰素-γ(IFN-γ)是一种促炎细胞因子,在抵抗布鲁氏菌感染的防御机制中发挥关键作用。据报道,IFN-γ 在(1 号内含子中的 +874A/T 和 +5644T/A)TT 和 +5644T/A、TT 基因型中产生较高的 IFN,与伊朗人群易患布鲁氏菌病有关。通过等位基因特异性聚合酶链反应方法对这些 IFN-γ 变体进行基因分型,在 281 名受试者中进行,包括 153 名活动性布鲁氏菌病患者和 128 名健康对照者。结果发现,+874 次要等位基因(A)和纯合基因型(AA)在布鲁氏菌病患者中比在对照组中更频繁存在(OR=2.588;95%CI,1.313-5.104;P=0.006 用于 AA 基因型;OR=1.575;95%CI,1.124-2.216;P=0.010 用于 A 等位基因)。然而,在患者和对照组之间,IFN-γ 多态性在 UTR5644A>T 位置的等位基因和基因型分布没有显著差异(P>0.05)。在这项研究中,单倍型的分布表明,T/A 单倍型(+874/UTR5644)在对照组中比在患者中更常见,可能保护受试者免受布鲁氏菌感染。研究表明,IFN-γ+874AA 基因型和 A 等位基因是伊朗人群发生布鲁氏菌病感染的危险因素。

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