Molecular, serological and population studies of the alleles and products of HLA-B*41.

C Darke, S Winkler, M G Guttridge, J Street, M Thomas, J Thompson, S McNamara
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引用次数: 4

Abstract

The HLA-B41 specificity was first identified over 25 years ago and, although both serological and biochemical studies have suggested its subdivision, it is only recently that two HLA-B*41 alleles (B*4101 and B*4102) have been identified and sequenced. We designed three oligonucleotide primers, combined in two mixtures to define these alleles by PCR using sequence-specific primers (PCR-SSP) in a random normal population of 9,464 HLA-A, B, DR, DQ typed Northern European Caucasoid donors from the Welsh Bone Marrow Donor Registry. The HLA-B41 phenotype frequency was 0.835%, and of the 79 HLA-B41 subjects 22 (27.85%) were B*4101 and 57 (72.15%) were B*4102. The phenotype frequencies of B*4101 and B*4102 were 0.232 and 0.602%, respectively, and the gene frequencies were 0.00116 and 0.00301, respectively. Formal two-locus linkage disequilibrium (LD) analysis demonstrated significant associations between B*4101 and A30 and DR11, and between B*4102 and A66 and DR13. LD analysis of three loci showed significant associations between B*4101, DR7, DQ2 and B*4101, DR11, DQ7 (DQB1*0301/0304) and between HLA-A3, B*4102, DR13; A66, B*4102, DR7; A66, B*4102, DR13; B*4102, DR13, DQ6 and B*4102, DR13, DQ7. Examination of the HLA phenotypes (including HLA-C) of the B*41 subjects, together with the LD analysis findings, suggested four different HLA haplotypes bearing B*4101 and five B*4102 haplotypes. The most frequent B*4101 haplotype was: HLA- A30 or other A allele, Cw*1701, B*4101, DRB1*1102, DQB1*0301 and the most freqent B*4102 haplotype was: A*6601 or A3 or other A allele, Cw*1701, B*4102, DRB1*1303, DQB1*0301. In addition, the well-known association of A66 with B41 was between A*6601 and B*4102, and although both B*41 alleles were commonly in association with Cw*1701, B*4101 was found with Cw*07. One-dimensional isoelectric focusing (1D-IEF) analysis of HLA-B proteins from 2 B*4101 and 2 B*4102 subjects clearly showed that the B41.1 and B41.2 1D-IEF variants, identified in the 10th International Histocompatibility Workshop, corresponded to B*4101 and B*4102 products, respectively. Serological titration studies, with 59 lymphocytotoxic pregnancy antisera, containing an HLA-B41 component and stimulated by up to five different HLA-B specificities, were unable to differentiate the two groups of B*41 subjects. This suggests that partition of the HLA-B41 specificity will not normally be achieved by classical serological methods. It is suggested that the previous alleged serological subdivision of HLA-B41 was founded on the unwitting use of antisera detecting the HLA-Cw*17 products.

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HLA-B*等位基因和产物的分子、血清学和群体研究
HLA-B41特异性在25年前首次被发现,尽管血清学和生化研究都表明其细分,但直到最近才发现两个HLA-B*41等位基因(B*4101和B*4102)并对其进行测序。我们设计了三种寡核苷酸引物,结合在两种混合物中,利用序列特异性引物(PCR- ssp)在威尔士骨髓供体登记处的9464名HLA-A、B、DR、DQ型北欧高加索人的随机正常人群中,通过PCR定义这些等位基因。HLA-B41表型频率为0.835%,79例HLA-B41患者中B*4101 22例(27.85%),B*4102 57例(72.15%)。B*4101和B*4102的表型频率分别为0.232和0.602%,基因频率分别为0.00116和0.00301。形式双位点连锁不平衡(LD)分析表明,B*4101与A30和DR11、B*4102与A66和DR13具有显著的相关性。3个位点的LD分析显示,B*4101、DR7、DQ2与B*4101、DR11、DQ7 (DQB1*0301/0304)、HLA-A3、B*4102、DR13之间存在显著相关性;A66, b *4102, dr7;A66, b *4102, dr13;B*4102, DR13, DQ6和B*4102, DR13, DQ7。检测B*41受试者的HLA表型(包括HLA- c)并结合LD分析结果,发现4种不同的HLA单倍型携带B*4101和5种B*4102单倍型。最常见的B*4101单倍型为:HLA- A30或其他A等位基因,Cw*1701、B*4101、DRB1*1102、DQB1*0301;最常见的B*4102单倍型为:A*6601或A3或其他A等位基因,Cw*1701、B*4102、DRB1*1303、DQB1*0301。此外,众所周知,A66与B41的关联在A*6601和B*4102之间,尽管B*41等位基因与Cw*1701普遍存在关联,但B*4101与Cw*07存在关联。对来自2 B*4101和2 B*4102受试者的HLA-B蛋白进行一维等电聚焦(1D-IEF)分析清楚地表明,在第10届国际组织相容性研讨会上鉴定的B41.1和B41.2 1D-IEF变体分别对应于B*4101和B*4102产品。用59种含有HLA-B41成分的淋巴细胞毒性妊娠抗血清进行血清学滴定研究,并通过多达五种不同的HLA-B特异性刺激,无法区分两组B*41受试者。这表明,传统的血清学方法通常无法实现HLA-B41特异性的划分。这表明,先前所谓的HLA-B41的血清学细分是建立在不知情的使用抗血清检测HLA-Cw*17产品。
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