Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
Stanford Blood Center, Stanford University School of Medicine, Palo Alto, CA, USA.
Hum Immunol. 2019 Jul;80(7):429-436. doi: 10.1016/j.humimm.2019.02.005. Epub 2019 Feb 11.
Next-generation sequencing (NGS) at the HLA-A, -B, -C, -DPA1, -DPB1, -DQA1, -DQB1, -DRB1 and -DRB3/4/5 loci was performed on 282 healthy unrelated individuals from different major regions of Spain. High-resolution HLA genotypes defined by full sequencing of class I loci and extended coverage of class II loci were obtained to determine allele frequencies and also to estimate extended haplotype frequencies. HLA alleles were typed at the highest resolution level (4-field level, 4FL); with exception of a minor deviation in HLA-DPA1, no statistically significant deviations from expected Hardy Weinberg Equilibrium (HWE) proportions were observed for all other HLA loci. This study provides new 4FL-allele and -haplotype frequencies estimated for the first time in the Spanish population. Furthermore, our results describe extended haplotypes (including the less frequently typed HLA-DPA1 and HLA-DQA1 loci) and show distinctive haplotype associations found at 4FL-allele definition in this Spanish population study. The distinctive allelic and haplotypic diversity found at the 4FL reveals the high level of heterozygosity and specific haplotypic associations displayed that were not apparent at 2-field level (2FL). Overall, these results may contribute as a useful reference source for future population studies, for HLA-disease association studies as a healthy control group dataset and for improving donor recruitment strategies of bone marrow registries. HLA genotyping data of this Spanish population cohort was also included in the 17th International Histocompatibility and Immunogenetics Workshop (IHIW) as part of the study of HLA diversity in unrelated worldwide populations using NGS.
对来自西班牙不同主要地区的 282 名健康无关个体进行了 HLA-A、-B、-C、-DPA1、-DPB1、-DQA1、-DQB1、-DRB1 和 -DRB3/4/5 基因座的下一代测序 (NGS)。通过对 I 类基因座进行全长测序和对 II 类基因座进行扩展覆盖,获得了高分辨率 HLA 基因型,以确定等位基因频率,并估计扩展单倍型频率。HLA 等位基因在最高分辨率水平(4 字段水平,4FL)进行分型;除 HLA-DPA1 略有偏差外,所有其他 HLA 基因座均未观察到与预期 Hardy Weinberg 平衡(HWE)比例有统计学显著偏差。本研究首次提供了西班牙人群中估计的新的 4FL 等位基因和单倍型频率。此外,我们的结果描述了扩展单倍型(包括较少分型的 HLA-DPA1 和 HLA-DQA1 基因座),并显示了在该西班牙人群研究中 4FL 等位基因定义时发现的独特单倍型关联。在 4FL 中发现的独特等位基因和单倍型多样性显示出高水平的杂合性和特定的单倍型关联,这在 2 字段水平(2FL)并不明显。总体而言,这些结果可能作为未来人群研究、作为健康对照组数据集的 HLA 疾病关联研究以及改善骨髓登记处供体招募策略的有用参考来源。该西班牙人群队列的 HLA 基因分型数据还被纳入第 17 届国际组织相容性和免疫遗传学研讨会(IHIW),作为使用 NGS 研究全球无关人群 HLA 多样性的一部分。