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HLA相关疾病的分子遗传学

The molecular genetics of HLA-related disorders.

作者信息

Bell J I

机构信息

Department of Medicine, Stanford University School of Medicine, California 94305.

出版信息

Ciba Found Symp. 1987;130:197-214. doi: 10.1002/9780470513507.ch12.

Abstract

The HLA region on the short arm of chromosome 6 contains a set of highly polymorphic loci responsible for regulating the immune response. Particular haplotypes, defined serologically, have been associated with a risk of developing certain autoimmune diseases such as insulin-dependent (juvenile-onset) diabetes mellitus, multiple sclerosis and rheumatoid arthritis. Recent developments in molecular biology have permitted an improved resolution of the locus and of the sequential arrangement of the susceptibility determinants on these haplotypes. Restriction fragment length polymorphisms have allowed subdivisions of serological haplotypes to be made. These correlate with disease susceptibility in some cases. Amplification of specific HLA class II alleles and nucleic acid sequencing have resulted in the identification of the structural determinants in the HLA that underlie some of these diseases.

摘要

位于6号染色体短臂上的HLA区域包含一组高度多态性位点,负责调节免疫反应。通过血清学定义的特定单倍型与患某些自身免疫性疾病的风险相关,如胰岛素依赖型(青少年发病型)糖尿病、多发性硬化症和类风湿性关节炎。分子生物学的最新进展使得对这些单倍型上的位点及其易感性决定因素的序列排列有了更高的分辨率。限制性片段长度多态性使得能够对血清学单倍型进行细分。在某些情况下,这些细分与疾病易感性相关。特定HLA II类等位基因的扩增和核酸测序已导致确定了HLA中一些这些疾病所基于的结构决定因素。

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