Progressing investigation of HLA-B* 51:36 in Liaoning region
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摘要: 目的:调查分析HLA-B*51:36在辽宁地区基因频率。方法:用PCR-SSP、SSO和SBT方法对50 000例辽宁健康人群进行HLA-A、B、DR基因分型,统计其中HLA-B*51:36的有关信息,并进行分析说明。使用微量淋巴细胞毒试验测定其中1例HLA-B*51:36样本的血清学Ⅰ类抗原特异性。结果:检出34例HLA-B*51:36,基因频率为0.068%,占B*51位点的0.42%。对其中1例先证者进行家系调查分析其单体型遗传规律为HLA-A*03-B*51:36-DRB1*01,检测其中1例样本血清学结果为B44、B51、B37。结论:B*51-DRB1*01显著的连锁不平衡。DRB1*01可能促使B*51:08更易发生基因位点特异性碱基突变从而形成了B*51:36。抗原特异性出现三联体现象为检测样本特有还是HLA-B*51:36碱基突变影响氨基酸表达产生的位点特异性结果,仍需多个相关样本进一步试验分析原因。
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关键词:
- HLA-B*51:36 /
- 连锁不平衡 /
- 三联体
Abstract: Objective: To analyze relevant information on HLA-B*51: 36 which was first found by the Hangzhou Blood Center in 2004.Methods: We performed low-and medium-resolution DNA typing of human leukocyte antigen(HLA)-A, B and DR alleles using polymerase chain reaction/sequence-specific primer or sequence-specific oligonucleotide prode and analyzed correlating information of HLA-B*51: 36. At the same time, we identified the HLA-B*51: 36 phenotype of one sample by the microlymphocytotoxicity test.Results: We detected 34 cases of HLA-B*51: 36 within 50 000 voluntary donors of Liaoning hemopoietic stem cell or platelet from 2004 to 2018.Conclusion: The results showed that HLA-B*51: 36-DR01 expressed strong linkage disequilibrium. However, in Liaoning, HLA-B*51-DR*01 trabant expressed no relationship of linkage. Our study suggested that DRB1*01 may prompt B*51: 08 gene site-specific mutation into gene type B*51: 36. The phenotype of the sample which had the HLA-B*51: 36 carried three HLA-B antigens, B44, B51 and B37. We need more samples to test so that we can analyze the causation of triple HLA-B antigen in the detected sample or the HLA-B*51: 36 allele.-
Key words:
- HLA-B*51:36 /
- linkage disequilibrium /
- HLA triplet
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