Sacks S H, Bushell A, Rust N A, Karagiannis J A, Jewell D P, Ledingham J G, Wood K J, McMichael A J
Nuffield Department of Medicine, John Radcliffe Hospital, Headington, Oxford, England.
Hum Immunol. 1987 Oct;20(2):175-87. doi: 10.1016/0198-8859(87)90031-0.
HLA class II beta-chain polymorphism was investigated in the haplotype HLA-DR3 to determine if patients with HLA-DR3-associated diseases express normal or variant class II polymorphisms. Analysis was carried out by two-dimensional gel electrophoresis of immunoprecipitated HLA class II molecules, DNA hybridization with DR beta and DQ beta gene probes on Taq 1, Bam H1, or Rsa 1 digests, and mixed lymphocyte culture. Two subtypes of HLA-DR3 were identified in normal homozygous DR3 individuals on the basis of polymorphism in one of two DR beta chains detected, corresponding to differences in DR beta restriction fragment patterns. These polymorphisms exhibited significant linkage disequilibrium with the A1,B8,DR3 and B18,DR3 haplotypes, respectively. In proliferative experiments, cells with the B18,DR3-associated polymorphism strongly stimulated cells from donors with the B8,DR3-related polymorphism, suggesting that a T-cell epitope recognized by B8,DR3 cells lies on the B18,DR3-associated DR beta chain. In seven HLA-DR3 homozygous patients with celiac disease and three HLA-DR3-homozygous patients with idiopathic membranous nephropathy, only the normal patterns of HLA class II molecules were displayed, the B8,DR3 type occurring in all patients and the B18,DR3 type in one patient. These data suggest that celiac disease and idiopathic membranous nephropathy are not related to disease-specific HLA-DR beta or -DQ beta gene variants within the DR3 population that are revealed by these methods.
对单倍型HLA - DR3中的HLA II类β链多态性进行了研究,以确定患有HLA - DR3相关疾病的患者表达的是正常还是变异的II类多态性。通过对免疫沉淀的HLA II类分子进行二维凝胶电泳、用DRβ和DQβ基因探针与Taq 1、Bam H1或Rsa 1酶切片段进行DNA杂交以及混合淋巴细胞培养来进行分析。根据检测到的两条DRβ链之一的多态性,在正常纯合DR3个体中鉴定出两种HLA - DR3亚型,这与DRβ限制性片段模式的差异相对应。这些多态性分别与A1、B8、DR3和B18、DR3单倍型表现出显著的连锁不平衡。在增殖实验中,具有B18、DR3相关多态性的细胞强烈刺激来自具有B8、DR3相关多态性供体的细胞,这表明B8、DR3细胞识别的T细胞表位位于B18、DR3相关的DRβ链上。在7例患有乳糜泻的HLA - DR3纯合患者和3例患有特发性膜性肾病的HLA - DR3纯合患者中,仅显示出HLA II类分子的正常模式,所有患者均出现B8、DR3型,1例患者出现B18、DR3型。这些数据表明,通过这些方法揭示的乳糜泻和特发性膜性肾病与DR3群体中疾病特异性的HLA - DRβ或 - DQβ基因变异无关。