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进行性自身免疫性β细胞功能不全:在无高危HLA等位基因DR3、DR4的情况下发生。

Progressive autoimmune beta cell insufficiency: occurrence in the absence of high-risk HLA alleles DR3, DR4.

作者信息

Eisenbarth G S, Srikanta S, Fleischnick E, Ganda O P, Jackson R A, Brink S J, Soeldner J S, Yunis E J, Alper C

出版信息

Diabetes Care. 1985 Sep-Oct;8(5):477-80. doi: 10.2337/diacare.8.5.477.

Abstract

In a prospective screening program for type I diabetes mellitus, we identified a unique family in which several members (mother and three siblings) expressed an unusual set of HLA-DR alleles (DR2+, DR3/4-) and were in different phases of immunologically mediated islet beta cell dysfunction. Immunologic and/or clinical manifestations of type I diabetes were absent in all siblings not sharing both HLA haplotypes in common with the proband. This article illustrates: the clinical utility of prospective family screening for predictive markers, such as islet cell antibodies, progressive autoimmune beta cell destruction can occur in the absence of the "high-risk" alleles HLA-DR3 and DR4, and HLA identity with the proband, rather than specific HLA alleles, i.e., presence of DR3, DR4 and absence of DR2, is an essential factor.

摘要

在一项针对I型糖尿病的前瞻性筛查项目中,我们发现了一个独特的家族,其中几名成员(母亲和三个兄弟姐妹)表达了一组不同寻常的HLA - DR等位基因(DR2 +,DR3/4 -),并且处于免疫介导的胰岛β细胞功能障碍的不同阶段。与先证者没有共享两个HLA单倍型的所有兄弟姐妹均未出现I型糖尿病的免疫和/或临床表现。本文说明:前瞻性家族筛查对于预测标志物(如胰岛细胞抗体)的临床实用性,在没有“高危”等位基因HLA - DR3和DR4的情况下,渐进性自身免疫性β细胞破坏也可能发生,并且与先证者的HLA一致性而非特定的HLA等位基因(即存在DR3、DR4且不存在DR2)是一个关键因素。

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