Typing of HLA-B*15 alleles using sequence-specific primers

被引:10
|
作者
Yu, N
Ohashi, M
Alosco, S
Salazar, M
Cao, K
Vina, MF
Yunis, EJ
机构
[1] Amer Red Cross, Blood Serv, HLA Lab, Dedham, MA 02026 USA
[2] Amer Red Cross, Natl Histocompatibil Lab, Bethesda, MD 20814 USA
[3] Harvard Univ, Sch Med, Dept Pathol, Cambridge, MA 02138 USA
[4] Dana Farber Canc Inst, Dept Immunol Canc & AIDS, Boston, MA 02115 USA
来源
TISSUE ANTIGENS | 1998年 / 52卷 / 03期
关键词
allele; antigen; HLA-B15; PCR-SSP; serology; transplantation;
D O I
10.1111/j.1399-0039.1998.tb03041.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have developed a DNA based typing method to detect 38 known B*15 alleles using sequence-specific primers (PCR-SSP). This method involves 38 primers and 39 PCR-SSP reactions with results that can be obtained in 3 hours The method is easy, fast and suitable fur clinical typing for bone marrow and organ transplantation. We have typed 106 HLA-B15 samples using this method. For homozygous HLA-B15 samples, some B*15 allele combinations need to be resolved by additional PCR reactions not included in this article. The method allows the detection of potential new alleles requiring sequencing for confirmation, and it is useful to resolve unusual serological reaction patterns for different HLA-B15 serological specificities. In addition, it could be used to resolve ambiguous PCR-SSOP typing results and for recognition of mismatches in serologically matched unrelated individuals.
引用
收藏
页码:260 / 269
页数:10
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