Routine HLA-B genotyping with PCR-sequence-specific oligonucleotides (PCR-SSO) detects eight new alleles: B*0807, B*0809, B*1551, B*3529, B*3532, B*4025, B*5304 and B*5508

被引:7
作者
Kennedy, CT [1 ]
Dodd, R [1 ]
Le, T [1 ]
Wallace, R [1 ]
Ng, G [1 ]
Greville, WD [1 ]
Kennedy, A [1 ]
Taverniti, A [1 ]
Moses, JH [1 ]
Clow, N [1 ]
Watson, N [1 ]
Dunckley, H [1 ]
机构
[1] Australian Red Cross Blood Serv, Mol Genet Lab, Sydney, NSW 2000, Australia
来源
TISSUE ANTIGENS | 2000年 / 55卷 / 03期
关键词
HLA-B*0807; HLA-B*0809; HLA-B*1551; HLA-B*3529; HLA-B*3532; HLA-B*4025; HLA-B*5304; HLA-B*5508; oligotyping;
D O I
10.1034/j.1399-0039.2000.550311.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
This paper describes eight new alleles (B*0807, B*0809, B*1551, B*3529, B*3532, B*4025, B*5304 and B*5508) that have been found by routine HLA-B genotyping with sequence specific oligonucleotides (SSOs). All of the new alleles have variations which cause changes in residues that occur within antigen binding pockets and T-cell recognition sites of the antigen. The new polymorphisms within these new alleles may affect the nature and specificity of peptide binding and cause differential T-cell activation, which may have an affect in transplantation.
引用
收藏
页码:266 / 270
页数:5
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