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外周血单个核细胞中HLA-DQ等位基因的差异表达:与1型自身免疫性糖尿病易感性和保护性相关的等位基因

Differential expression of HLA-DQ alleles in peripheral blood mononuclear cells: alleles associated with susceptibility to and protection from autoimmune type 1 diabetes.

作者信息

Britten A C, Mijovic C H, Barnett A H, Kelly M A

机构信息

Department of Medicine, Division of Medical Sciences, University of Birmingham, Birmingham, UK.

出版信息

Int J Immunogenet. 2009 Feb;36(1):47-57. doi: 10.1111/j.1744-313X.2008.00823.x.

DOI:10.1111/j.1744-313X.2008.00823.x
PMID:19207936
Abstract

Differential expression of human leucocyte antigen (HLA) class II genes has been postulated to influence the risk of developing autoimmune disease. In this study, we investigated the relationship between the level of mRNA expression of DQA1 and DQB1 alleles in peripheral blood mononuclear cells and the influence of the alleles on susceptibility to type 1 diabetes (T1D). Transcripts from pairs of DQA1 and DQB1 alleles were quantified in 59 DQ-heterozygous individuals (29 patients with T1D and 30 healthy control subjects). Luciferase reporter gene assays were used to investigate the relative promoter activities of the alleles associated with high and low risk of disease. DQA10301 and the DQB106 group of alleles (*0601, 0602, 0603 and 0604) were generally overexpressed in comparison to other alleles. In contrast, mRNA for DQB10201/0202 was generally less abundant than other DQB1 transcripts. These data correlated well with the relative promoter activities observed for the diabetes-associated alleles; the strongest promoters were those derived from DQA10301 and DQB10602, while a 700-bp fragment derived from the DQB10201 promoter showed the lowest activity of the DQB1 constructs. There was no simple correlation between the level of expression of specific DQ alleles and their influence on the risk of diabetes. The functional relevance of our findings and their implications for the pathogenesis of autoimmunity remain to be determined.

摘要

据推测,人类白细胞抗原(HLA)II类基因的差异表达会影响自身免疫性疾病的发病风险。在本研究中,我们调查了外周血单个核细胞中DQA1和DQB1等位基因的mRNA表达水平之间的关系,以及这些等位基因对1型糖尿病(T1D)易感性的影响。对59名DQ杂合个体(29例T1D患者和30名健康对照者)的DQA1和DQB1等位基因对的转录本进行了定量分析。使用荧光素酶报告基因测定法研究与疾病高风险和低风险相关的等位基因的相对启动子活性。与其他等位基因相比,DQA10301和DQB106等位基因组(0601、0602、0603和0604)通常过表达。相比之下,DQB10201/0202的mRNA通常比其他DQB1转录本少。这些数据与观察到的糖尿病相关等位基因的相对启动子活性密切相关;最强的启动子来自DQA10301和DQB10602,而来自DQB1*0201启动子的700 bp片段在DQB1构建体中活性最低。特定DQ等位基因的表达水平与其对糖尿病风险的影响之间没有简单的相关性。我们研究结果的功能相关性及其对自身免疫发病机制的影响仍有待确定。

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