Liu Jie, Quan Zhan-Rou, Zhu Tian-Hui, Zhong Yan-Ping, Jiang Ren-Hui, Yang Bing-Na, Zhang Yin-Ming, Song Jia-Min, Zou Hong-Yan, Deng Zhi-Hui
Institute of Blood Transfusion Medicine, Shenzhen Blood Center, Shenzhen, Guangdong, China.
Immunogenetics Laboratory, Shenzhen Blood Center, Shenzhen, Guangdong, China.
HLA. 2025 Apr;105(4):e70148. doi: 10.1111/tan.70148.
Although the allele and haplotype frequencies of 11 HLA loci (HLA-A, B, C, DRB1, DRB3/4/5, DQA1, DQB1, DPA1 and DPB1) have been reported in different populations, rare studies have simultaneously assessed the allele distributions of non-classical HLA class I genes (HLA-E/F/G/H) and MICA/MICB together with the 11 classical HLA loci, or further analysed the haplotype frequencies covering the 17 loci. The present study aims to investigate the allele diversity and haplotype frequencies of 17 HLA-related loci including HLA genes and MICA/MICB simultaneously using a hybrid capture (HC)-based NGS method. A total of 358 HLA alleles including 177 class I and 137 class II alleles, as well as 29 MICA and 15 MICB alleles were identified in this project. The most frequent alleles at each locus were A11:01 (29.10%), B40:01 (14.46%), C01:02 (19.90%), DRB109:01 (15.61%), DQB103:01 (18.48%), DPB105:01 (40.13%), DQA101:02 (22.58%), DPA102:02 (55.27%), DRB302:02 (65.95%), DRB401:03 (95.20%), DRB501:01 (75.97%), E01:03 (62.63%), F01:01 (97.07%), G01:01 (70.74%), H01:01 (35.87%), MICA010:01 (19.90%) and MICB005:02 (57.53%), respectively. The haplotype frequencies for different combinations of HLA loci were estimated and linkage disequilibrium (LD) between alleles for all pairs of neighbouring loci were calculated. The most frequent haplotype covering 17 loci was F01:01-G01:01-H01:01-A02:07-E01:03-C01:02-B46:01-MICA010:01-MICB005:02-DRB401:03-DRB109:01-DQA103:02-DQB103:03-DPA102:02-DPB105:01 with a frequency of 3.18%. This is the first study on allelic polymorphism, haplotype inference and LD covering 17 HLA-related loci simultaneously in the Shenzhen Chinese population. These results will extend our knowledge of the allelic diversity of the HLA complex and provide population genetics data for transplantation and HLA-associated disease studies.
尽管已有不同人群中11个HLA基因座(HLA - A、B、C、DRB1、DRB3/4/5、DQA1、DQB1、DPA1和DPB1)的等位基因和单倍型频率的报道,但很少有研究同时评估非经典HLA I类基因(HLA - E/F/G/H)和MICA/MICB与这11个经典HLA基因座的等位基因分布,或进一步分析涵盖这17个基因座的单倍型频率。本研究旨在使用基于杂交捕获(HC)的二代测序方法,同时研究包括HLA基因和MICA/MICB在内的17个HLA相关基因座的等位基因多样性和单倍型频率。本项目共鉴定出358个HLA等位基因,包括177个I类等位基因和137个II类等位基因,以及29个MICA等位基因和15个MICB等位基因。每个基因座最常见的等位基因分别为A11:01(29.10%)、B40:01(14.46%)、C01:02(19.90%)、DRB109:01(15.61%)、DQB103:01(18.48%)、DPB105:01(40.13%)DQA101:02(22.58%)、DPA102:02(55.27%)、DRB302:02(65.95%)、DRB401:03(95.20%)、DRB501:01(75.97%)、E01:03(62.63%)、F01:01(97.07%)、G01:01(70.74%)、H01:01(35.87%)、MICA010:01(19.90%)和MICB005:02(57.53%)。估计了HLA基因座不同组合的单倍型频率,并计算了所有相邻基因座对之间等位基因的连锁不平衡(LD)。涵盖17个基因座最常见的单倍型是F01:01 - G01:01 - H01:01 - A02:07 - E01:03 - C01:02 - B46:01 - MICA010:01 - MICB005:02 - DRB401:03 - DRB109:01 - DQA103:OB - DQB103:03 - DPA102:02-DPB105:01,频率为3.18%。这是首次在深圳汉族人群中同时对涵盖17个HLA相关基因座的等位基因多态性、单倍型推断和LD进行研究。这些结果将扩展我们对HLA复合体等位基因多样性的认识,并为移植和HLA相关疾病研究提供群体遗传学数据。