Limas C, Limas C J, Boudoulas H, Bair R, Graber H, Sparks L, Wooley C F
Department of Laboratory Medicine and Pathology, University of Minnesota Medical School, Minneapolis 55455.
Am Heart J. 1994 Feb;127(2):382-6. doi: 10.1016/0002-8703(94)90128-7.
The presence of beta-receptor autoantibodies and their relationship to restriction fragment length polymorphisms of the human leukocyte antigen (HLA) class II genes were studied in 42 affected and unaffected members of a family with a heritable disorder of the conduction system and cardiac muscle. Antibodies were detected in 34% of all members (59% of affected and 22% of unaffected; p < 0.01). Significant differences between affected and unaffected individuals and between anti-beta-receptor antibody positive and negative individuals were noted in the prevalence of polymorphisms obtained with Taq I for the HLA-DR beta and HLA-DQ alpha genes. In affected individuals, there was a strong positive correlation between these polymorphisms and the presence of anti-beta-receptor antibodies. These results suggest that autoimmune mechanisms under the control of the class II genes play an important role in the pathogenesis of familial cardiomyopathy.
在一个患有遗传性传导系统和心肌疾病的家族中,对42名患病和未患病成员进行了β受体自身抗体的检测及其与人类白细胞抗原(HLA)Ⅱ类基因限制性片段长度多态性的关系研究。在所有成员中,34%检测到抗体(患病成员中为59%,未患病成员中为22%;p<0.01)。对于HLA-DRβ和HLA-DQα基因,用TaqⅠ获得的多态性患病率在患病个体与未患病个体之间以及抗β受体抗体阳性与阴性个体之间存在显著差异。在患病个体中,这些多态性与抗β受体抗体的存在之间存在强正相关。这些结果表明,Ⅱ类基因控制下的自身免疫机制在家族性心肌病的发病机制中起重要作用。