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首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Association of IFN-gamma and IFN regulatory factor 1 polymorphisms with childhood atopic asthma.
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Association of IFN-gamma and IFN regulatory factor 1 polymorphisms with childhood atopic asthma.

机译:IFN-γ和IFN调节因子1多态性与儿童特应性哮喘的关联。

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BACKGROUND: IFN-gamma and related molecules play important roles in the differentiation and function of TH2 cells. OBJECTIVE: We sought to determine whether IFNG and related genes contribute to any susceptibility to atopic asthma, a representative TH2-dominant disorder. METHODS: We investigated the association of IFNG (CA repeat polymorphism within the first intron), IRF1 (GT repeat polymorphism within the intron 7), IFNGR1 (Val 14 Met), and IFNGR2 (Gln 64 Arg) gene polymorphisms with atopic asthma in the Japanese child population. RESULTS: A significant association (P =.0018) was observed between IFNG gene polymorphism and atopic asthma. The tendency was more prominent in patients with age of onset of 3 years or younger (P =.0004) or patients with a family history of allergic diseases (P =.0038). Furthermore, there was a significant association between IRF1 gene whole-allele distribution and atopic asthma (P =.044). The tendency was more prominent in patients with onset at 3 years of age or less (P =.0058). On the other hand, IFNGR1 and IFNGR2 gene polymorphisms showed no association with atopic asthma. CONCLUSION: These results suggested that among IFNG and related genes, IFNG and IRF1 genes confer genetic susceptibility to atopic asthma in Japanese children.
机译:背景:IFN-γ和相关分子在TH2细胞的分化和功能中起着重要作用。目的:我们试图确定IFNG和相关基因是否对特应性哮喘(一种典型的TH2显性疾病)有任何敏感性。方法:我们调查了IFNG(第一个内含子内的CA重复多态性),IRF1(内含子7内的GT重复多态性),IFNGR1(Val 14 Met)和IFNGR2(Gln 64 Arg)基因多态性与特应性哮喘的相关性。日本儿童人口。结果:IFNG基因多态性与特应性哮喘之间存在显着相关性(P = .0018)。发病年龄在3岁或更小(P = .0004)或有过敏性疾病家族史的患者(P = .0038),这种趋势更为明显。此外,IRF1基因全等位基因分布与特应性哮喘之间存在显着关联(P = .044)。在3岁或以下发病的患者中这种趋势更为明显(P = .0058)。另一方面,IFNGR1和IFNGR2基因多态性与特应性哮喘无关。结论:这些结果表明,在IFNG和相关基因中,IFNG和IRF1基因赋予日本儿童特应性哮喘遗传易感性。

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