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德国人群中的人类白细胞抗原(HLA)与发作性睡病

HLA and narcolepsy in a German population.

作者信息

Mueller-Eckhardt G, Meier-Ewert K, Schendel D J, Reinecker F B, Multhoff G, Mueller-Eckhardt C

出版信息

Tissue Antigens. 1986 Sep;28(3):163-9. doi: 10.1111/j.1399-0039.1986.tb00476.x.

Abstract

In this paper the first MHC data including HLA-A, B, C, DR, DQ and complement BF, C4A, C4B determinants in German narcoleptics are presented together with the first family studies in European Caucasoids. 57 out of 58 unrelated patients (98.3%) were positive for DR2 and DQw1, respectively. In contrast to all other reports, one patient with typical signs of narcolepsy was found to be DR2/DQw1 negative. Data showing significant increase in the frequency of B7, and normal frequencies of B35 were discordant with data from Japanese patients. Definition of the extended DR2 linked haplotypes, deduced from 6 families, revealed that 5 out of 12 were DQw1, DR2, BFS, C4B1, C4A3, B7 (Cw7), while 11/12 had DR2, DQw1, BFS, C4A3, C4B1 in common. In one multiple case family two genotypically different DR2 haplotypes were identified in affected siblings. Results from the family study were concordant with a dominant mode of inheritance with incomplete penetrance of a hypothetical disease susceptibility gene.

摘要

本文展示了德国发作性睡病患者的首批主要组织相容性复合体(MHC)数据,包括人类白细胞抗原(HLA)-A、B、C、DR、DQ以及补体BF、C4A、C4B决定簇,同时还展示了欧洲白种人的首批家系研究结果。58名无亲缘关系的患者中有57名(98.3%)分别为DR2和DQw1阳性。与所有其他报告不同的是,发现一名有发作性睡病典型症状的患者为DR2/DQw1阴性。显示B7频率显著增加以及B35频率正常的数据与日本患者的数据不一致。从6个家系推导得出的扩展DR2连锁单倍型的定义表明,12个中有5个是DQw1、DR2、BFS、C4B1、C4A3、B7(Cw7),而12个中有11个共同拥有DR2、DQw1、BFS、C4A3、C4B1。在一个有多发病例的家系中,在患病同胞中鉴定出两种基因型不同的DR2单倍型。家系研究结果与一种假设的疾病易感基因不完全外显的显性遗传模式一致。

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