Wallin J, Hillert J, Olerup O, Carlsson B, Ström H
Center for BioTechnology, Karolinska Institute, Novum, Sweden.
Arthritis Rheum. 1991 Nov;34(11):1416-24. doi: 10.1002/art.1780341112.
HLA-DR, HLA-DQ, and T cell receptor beta (TCR beta) chain gene polymorphisms were investigated in 43 patients with rheumatoid arthritis (RA), in 10 patients with Felty's syndrome (FS), and in 5 RA multicase families. RA was found to be strongly associated with a DRB1 gene sequence motif present in DR1, DR4-Dw4, and DR4-Dw14 alleles. Ninety-three percent of RA patients were positive for at least 1 of these alleles, providing strong support for the "shared epitope hypothesis." The frequency distribution of this sequence motif suggests a dominant mode of inheritance. All 10 FS patients were DR4-Dw4 positive. Different DR-DQ associations among DR4 positive RA and FS patients indicate heterogeneity in the genetic susceptibility to these 2 disease entities. Furthermore, analyses of TCR V beta 8, V beta 11, and C beta gene polymorphisms did not support the notion of an influence of TCR beta germline allotypes on RA susceptibility.
对43例类风湿关节炎(RA)患者、10例费尔蒂综合征(FS)患者以及5个RA多病例家庭进行了人类白细胞抗原DR(HLA - DR)、HLA - DQ和T细胞受体β(TCRβ)链基因多态性研究。发现RA与DR1、DR4 - Dw4和DR4 - Dw14等位基因中存在的DRB1基因序列基序密切相关。93%的RA患者至少携带其中1个等位基因,为“共同表位假说”提供了有力支持。该序列基序的频率分布提示其呈显性遗传模式。所有10例FS患者均为DR4 - Dw4阳性。DR4阳性的RA患者和FS患者中不同的DR - DQ关联表明这两种疾病实体在遗传易感性方面存在异质性。此外,对TCR Vβ8、Vβ11和Cβ基因多态性的分析不支持TCRβ种系同种异型对RA易感性有影响这一观点。