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内分泌系统自身免疫性疾病的免疫遗传标志物。

Immunogenetic markers for autoimmune diseases of the endocrine system.

作者信息

Badenhoop K

机构信息

II. Medizinische Klinik, Klinikum Mannheim der Universität Heidelberg, FRG.

出版信息

Klin Wochenschr. 1990;68 Suppl 21:10-4.

PMID:1973965
Abstract

New immunogenetic markers are demonstrated for type 1 diabetes mellitus, Graves' disease and Hashimoto's thyroiditis. These markers are detected by restriction fragment length polymorphism (RFLP) analysis of HLA-D region genes and genes for the tumor necrosis factor alpha (TNF alpha). By analysing haplotypes transmitted to diabetic probands in families and comparing them with haplotypes that are only transmitted to healthy siblings it is shown that DQw8-DQB1 gene variation is important for susceptibility on DR4 haplotypes. Analysis of this DQw3 split in patients with Hashimoto's thyroiditis reveals that the other DQB1 gene variation, namely DQw7, displays the strongest association with Hashimoto's thyroiditis. This DQB1 variation has several implications for susceptibility and/or pathogenesis of both autoimmune endocrine diseases. Novel polymorphisms for TNF alpha are detected and it is shown that heterozygosity for TNF polymorphisms is significantly associated with type I diabetes and Graves' disease. Furthermore, DR4 haplotypes transmitted to diabetic probands possess significantly more the 10.5 Kb fragment in contrast to DR4 haplotypes transmitted only to healthy family members. This genetic polymorphism raises functional issues in susceptibility to autoimmune disease and can lead to a new explanation of the enigmatic HLA-association with a variety of diseases.

摘要

已证实1型糖尿病、格雷夫斯病和桥本甲状腺炎有新的免疫遗传标记。这些标记通过对HLA - D区域基因和肿瘤坏死因子α(TNFα)基因进行限制性片段长度多态性(RFLP)分析来检测。通过分析传递给家族中糖尿病先证者的单倍型,并将其与仅传递给健康同胞的单倍型进行比较,结果表明DQw8 - DQB1基因变异对DR4单倍型的易感性很重要。对桥本甲状腺炎患者中这种DQw3分型的分析显示,另一种DQB1基因变异,即DQw7,与桥本甲状腺炎的关联最为强烈。这种DQB1变异对两种自身免疫性内分泌疾病的易感性和/或发病机制有多种影响。检测到TNFα的新型多态性,并且显示TNF多态性的杂合性与I型糖尿病和格雷夫斯病显著相关。此外,与仅传递给健康家庭成员的DR4单倍型相比,传递给糖尿病先证者的DR4单倍型明显更多地拥有10.5 Kb片段。这种基因多态性引发了自身免疫性疾病易感性方面的功能问题,并可能为HLA与多种疾病的神秘关联带来新的解释。

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