Clarkson R, Bate A S, Grennan D M, Chattopadhyay C, Sanders P, Davis M, Kelly C
Rheumatic Diseases Centre, Hope Hospital, Salford.
Ann Rheum Dis. 1990 Dec;49(12):976-9. doi: 10.1136/ard.49.12.976.
DQ beta and C4 null alleles have been defined in patients with rheumatoid arthritis, Felty's syndrome, and in control subjects. Comparison of DR4 positive subjects shows that rheumatoid disease without extra-articular features has no preferential associations with either DQ beta or C4 null variants. In Felty's syndrome there are significant associations with both the class II major histocompatibility complex (MHC) DQw7 allele (86% of DR4 positive patients with Felty's syndrome and 53% of DR4 positive controls) and the class III MHC C4B null allele (50% of patients with Felty's syndrome and 20% of DR4 positive controls). DQw7 and the C4B null allele are in linkage disequilibrium and the B44-Bf S-C4A3-C4B*Q0-DR4-DQw7 haplotype accounts for five of 24 DR4 positive haplotypes assigned in subjects with Felty's syndrome. The results were not accounted for by articular disease severity and suggest that articular and extra-articular forms of rheumatoid disease may be immunogenetically heterogeneous.
在类风湿关节炎、费尔蒂综合征患者以及对照受试者中已明确了DQβ和C4无效等位基因。对DR4阳性受试者的比较显示,无关节外表现的类风湿疾病与DQβ或C4无效变体均无优先关联。在费尔蒂综合征中,与II类主要组织相容性复合体(MHC)DQw7等位基因(86%的费尔蒂综合征DR4阳性患者和53%的DR4阳性对照)以及III类MHC C4B无效等位基因(50%的费尔蒂综合征患者和20%的DR4阳性对照)均存在显著关联。DQw7和C4B无效等位基因处于连锁不平衡状态,且B44 - BfS - C4A3 - C4B*Q0 - DR4 - DQw7单倍型占费尔蒂综合征受试者中分配的24个DR4阳性单倍型中的5个。结果并非由关节疾病严重程度所致,提示类风湿疾病的关节型和关节外型在免疫遗传学上可能是异质性的。