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意大利东北部乳糜泻患者白细胞介素-10基因启动子多态性

Interleukin-10 gene promoter polymorphisms in celiac patients from north-eastern Italy.

作者信息

Zupin Luisa, Polesello Vania, Catamo Eulalia, Crovella Sergio, Segat Ludovica

机构信息

Institute for Maternal and Child Health, IRCCS "Burlo Garofolo", Via dell'Istria 65/1, 34137 Trieste, Italy.

University of Trieste, Piazzale Europa 1, 34127 Trieste, Italy.

出版信息

Hum Immunol. 2014 Jul;75(7):656-61. doi: 10.1016/j.humimm.2014.04.011. Epub 2014 Apr 24.

Abstract

Celiac disease is a complex chronic intestinal disorder driven by an immune response against the gliadin fraction of gluten: many factors are involved in the pathogenesis of the disease, and among these Interleukin-10 could play an important role. In the present study, the -1082A>G, -819T>C and -592A>C IL10 functional polymorphisms were analyzed in 565 celiac patients and 576 healthy controls from north-eastern Italy, stratified for HLA class II celiac disease risk haplotypes. No significant differences were observed for the three IL10 polymorphisms distribution between celiac patients and controls with the exception of a slightly increased risk for the -1082A allele in HLA-DQ8 male individuals. Although our findings suggest that the IL10 genetic variants analyzed do not have a major role in the susceptibility to the development of celiac disease in north-eastern Italian patients, we think that the possible involvement of IL10 gene in CD should deserve further investigation and that large-scale studies are recommended to confirm our findings.

摘要

乳糜泻是一种复杂的慢性肠道疾病,由针对麸质中麦醇溶蛋白部分的免疫反应驱动:许多因素参与了该疾病的发病机制,其中白细胞介素-10可能起重要作用。在本研究中,对来自意大利东北部的565例乳糜泻患者和576例健康对照进行了IL10功能多态性-1082A>G、-819T>C和-592A>C的分析,并根据HLA II类乳糜泻风险单倍型进行分层。除了HLA-DQ8男性个体中-1082A等位基因的风险略有增加外,在乳糜泻患者和对照之间未观察到三种IL10多态性分布的显著差异。尽管我们的研究结果表明,所分析的IL10基因变异在意大利东北部患者患乳糜泻的易感性中没有主要作用,但我们认为IL10基因在乳糜泻中的可能作用值得进一步研究,建议进行大规模研究以证实我们的发现。

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