Functional characterization and exon 2 intron 2 exon 3 gene sequence of HLA-B*2712 as found in a British family

被引:8
作者
Hemmatpour, SK
Dunn, PPJ
Evans, PR
Green, A
Howell, WM
机构
[1] Southampton Gen Hosp, Histocompatibil & Immunogenet Lab, Southampton SO16 6YD, Hants, England
[2] UKTSSA, Bristol BS34 8RR, Avon, England
[3] Natl Blood Serv, Bristol Ctr, Bristol BS10 5ND, Avon, England
来源
EUROPEAN JOURNAL OF IMMUNOGENETICS | 1998年 / 25卷 / 06期
关键词
D O I
10.1046/j.1365-2370.1998.00126.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The HLA-B*27 group of alleles has been extensively studied due to the association of particular B*27 alleles with ankylosing spondylitis (AS). We describe here an HLA-B*27 allele (B*2712) encoding an antigen that lacks reactivity with B27 monoclonal antibodies (moabs) and alloantisera but reacts with some B40/B60 moabs and alloantisera and expresses the Bw6 public epitope. This allele was discovered by the segregation of an HLA-B allele undetectable by PCR-SSP within a Caucasian family from the British population referred for routine bone marrow transplant HLA typing and found in the haplotype A*29; B*2712; Cw*1203; DRB1*13; DQB1*0603. Serological typing showed a lack of reactivity with four B27 moabs and four alloantisera but positive reactivity with moabs and alloantisera specific for B40/B60 and Bw6 public epitopes. Subsequent sequencing showed the closest homology was with B*2708 with three mismatches in exon 2 at positions 204, 209 and 210. The intron 2 sequence was identical with other B*27 lineage alleles including a 2 base pair deletion at positions 95 and 96. The relationship between HLA-B*2712 and reported B60 associations with susceptibility to AS remains to be determined.
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收藏
页码:395 / 402
页数:8
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