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来自土耳其的结核病儿童的干扰素-γ基因和干扰素-γ受体-1基因多态性

Interferon-gamma gene and interferon-gamma receptor-1 gene polymorphisms in children with tuberculosis from Turkey.

作者信息

Onay Huseyin, Ekmekci Aslihan Yilmaz, Durmaz Burak, Sayin Eren, Cosar Hese, Bayram Nuri, Can Demet, Akin Haluk, Ozkinay Cihangir, Ozkinay Ferda

机构信息

Department of Medical Genetics, Ege University Faculty of Medicine, Bornova/Izmir, Turkey.

出版信息

Scand J Infect Dis. 2010;42(1):39-42. doi: 10.3109/00365540903253502.

Abstract

Macrophage activation by interferon-gamma (IFN-gamma) is important in host resistance to tuberculosis (TB). In this study, the relationships of the +874 T/A polymorphism in the first intron of the IFN-gamma gene and intronic (CA)n polymorphic microsatellite marker of the interferon-gamma receptor 1 (IFN-gammaR1) gene to TB susceptibility were investigated in children. Forty children with TB and 67 age-matched controls were included. There were no significant differences between the allele frequencies and genotype frequencies of patient and control groups for the polymorphism +874 T/A in the IFN-gamma gene. Differences that were not statistically significant were found between the group of children with TB and the control group for the allelic markers (170 and 180) in the IFN-gammaR1 gene. The incidence of the allele 170 was higher in patients (30.9%) than in controls (17.4%), whereas the allele 180 was found to be more common in controls (9% vs 1.2%). In conclusion, no significant association was observed between the +874 T/A polymorphism found in the first exon of the IFN-gamma gene and TB susceptibility in Turkish children.

摘要

γ-干扰素(IFN-γ)激活巨噬细胞在宿主抵抗结核病(TB)中起重要作用。在本研究中,我们调查了儿童中IFN-γ基因第一内含子中的+874 T/A多态性以及干扰素-γ受体1(IFN-γR1)基因的内含子(CA)n多态性微卫星标记与TB易感性的关系。研究纳入了40例TB患儿和67例年龄匹配的对照。IFN-γ基因中+874 T/A多态性的患者组和对照组的等位基因频率和基因型频率之间没有显著差异。在TB患儿组和对照组之间,IFN-γR1基因的等位基因标记(170和180)存在无统计学意义的差异。患者中170等位基因的发生率(30.9%)高于对照组(17.4%),而180等位基因在对照组中更为常见(9%对1.2%)。总之,在土耳其儿童中,未观察到IFN-γ基因第一外显子中发现的+874 T/A多态性与TB易感性之间存在显著关联。

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