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IDDM1中与HLA - DPB1相关的成分及其与主要基因座HLA - DQB1、-DQA1和-DRB1的关系。

The HLA-DPB1--associated component of the IDDM1 and its relationship to the major loci HLA-DQB1, -DQA1, and -DRB1.

作者信息

Cucca F, Dudbridge F, Loddo M, Mulargia A P, Lampis R, Angius E, De Virgiliis S, Koeleman B P, Bain S C, Barnett A H, Gilchrist F, Cordell H, Welsh K, Todd J A

机构信息

Department of Biomedical Science and Biotechnology, University of Cagliari, Italy.

出版信息

Diabetes. 2001 May;50(5):1200-5. doi: 10.2337/diabetes.50.5.1200.

Abstract

The major histocompatibility complex (MHC) HLA region on chromosome 6p21 contains the major locus of type 1 diabetes (IDDM1). Common allelic variants at the class II HLA-DRB1, -DQA1, and -DQB1 loci account for the major part of IDDM1. Previous studies suggested that other MHC loci are likely to contribute to IDDM1, but determination of their relative contributions and identities is difficult because of strong linkage disequilibrium between MHC loci. One prime candidate is the polymorphic HLA-DPB1 locus, which (with the DPA1 locus) encodes the third class II antigen-presenting molecule. However, the results obtained in previous studies appear to be contradictory. Therefore, we have analyzed 408 white European families (200 from Sardinia and 208 from the U.K.) using a combination of association tests designed to directly compare the effect of DPB1 variation on the relative predisposition of DR-DQ haplotypes, taking into account linkage disequilibrium between DPB1 and the DRB1, DQA1, and DQB1 loci. In these populations, the overall contribution of DPB1 to IDDM1 is small. The main component of the DPB1 contribution to IDDM1 in these populations appears to be the protection associated with DPB1*0402 on DR4-negative haplotypes. We suggest that the HLA-DP molecule itself contributes to IDDM1.

摘要

位于6号染色体p21区域的主要组织相容性复合体(MHC)HLA区包含1型糖尿病的主要位点(IDDM1)。II类HLA - DRB1、- DQA1和- DQB1位点的常见等位基因变异占IDDM1的主要部分。先前的研究表明,其他MHC位点可能也对IDDM1有影响,但由于MHC位点之间存在强连锁不平衡,确定它们的相对贡献和身份很困难。一个主要候选位点是多态性的HLA - DPB1位点,它(与DPA1位点一起)编码第三种II类抗原呈递分子。然而,先前研究获得的结果似乎相互矛盾。因此,我们分析了408个欧洲白人家系(200个来自撒丁岛,208个来自英国),采用了一系列关联测试的组合,旨在直接比较DPB1变异对DR - DQ单倍型相对易感性的影响,同时考虑DPB1与DRB1、DQA1和DQB1位点之间的连锁不平衡。在这些人群中,DPB1对IDDM1的总体贡献较小。在这些人群中,DPB1对IDDM1贡献的主要成分似乎是与DR4阴性单倍型上的DPB1 * 0402相关的保护作用。我们认为HLA - DP分子本身对IDDM1有影响。

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