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Sequence, genetics and serology of a new HLA-B allele: B*4903.

作者信息

Darke C, Street J, Guttridge M G

机构信息

Welsh Transplantation and Immunogenetics Laboratory, Welsh Blood Service, Pontyklun, United Kingdom.

出版信息

Tissue Antigens. 2001 May;57(5):478-80. doi: 10.1034/j.1399-0039.2001.057005478.x.

Abstract

A new HLA-B allele - B4903 - was detected by the polymerase chain reaction using sequence-specific priming (PCR-SSP), in a Caucasoid bone marrow panel donor, that differs from B4901 by 8 nucleotides at positions 141, 142, 144, 165, 167, 193, 206 and 213 in exon 2. These substitutions all occur in HLA-B51 and B52 alleles and encode 4 amino acid substitutions at positions 24 (Thr to Ala), 32 (Leu to Gln), 41 (Thr to Ala) and 45 (Lys to Thr). This suggests that B4903 occurred following a gene conversion-like event involving B4901 and probably a B51 allele. HLA-B4903 was identified on a haplotype with: HLA-A0201; Cw07; DRB11302/34; DRB30301; DQA10102; DQB10604; BfS; C4A3; C4BQ0 and encodes a unique serological specificity which was characterised by the reactivity of 55 antisera directed towards at least four predicted epitopes. No further examples of B*4903 were found in 15,796 consecutive HLA PCR-SSP typed donors from the Welsh Bone Marrow Donor Registry, indicating that this allele has a phenotype frequency of <0.01% and a gene frequency of <0.00004.

摘要

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