Report from the extended HLA-DPA1 ∼ promoter ∼ HLA-DPB1 haplotype of the 18th international HLA and immunogenetics workshop

被引:1
|
作者
Truong, Linh [1 ,2 ,9 ]
Matern, Benedict M. [3 ]
El-Lagta, Naser [1 ]
Mobegi, Fredrick M. [1 ]
Askar, Medhat [4 ]
Ogret, Yeliz [5 ]
Oguz, Fatma S. [5 ]
Kwok, Janette [6 ]
D'Orsogna, Lloyd [1 ,2 ]
Martinez, Patricia [1 ,2 ]
Petersdorf, Effie [7 ]
Tilanus, Marcel G. J. [8 ]
De Santis, Dianne [1 ,2 ]
机构
[1] Fiona Stanley Hosp, Dept Clin Immunol, PathWest, Perth, WA, Australia
[2] Univ Western Australia, UWA Med Sch, Perth, WA, Australia
[3] Univ Med Ctr Utrecht, Cent Diagnost Lab, Utrecht, Netherlands
[4] Qatar Univ, Coll Med, QU Hlth Cluster & Dept Basic Sci, Doha, Qatar
[5] Istanbul Univ, Istanbul Fac Med, Istanbul, Turkiye
[6] Queen Mary Hosp, Div Transplantat & Immunogenet, Hong Kong, Peoples R China
[7] Fred Hutchinson Canc Res Ctr, Clin Res Div, Seattle, WA USA
[8] Maastricht Univ, Sch Oncol & Reprod, GROW, Maastricht, Netherlands
[9] Fiona Stanley Hosp, Dept Clin Immunol, PathWest, 9-11 Robin Warren Dr, Murdoch, WA 6150, Australia
关键词
18th IHIWS report; HLA haplotype; TGS; DP EXPRESSION; REGION; RECOMBINATION; SELECTION; SEQUENCE; COMPLEX; EPITOPE; MAP;
D O I
10.1111/tan.15155
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The primary goal of the HLA-DPA1 similar to promoter similar to HLA-DPB1 haplotype component of the 18th IHIWS was to characterise the extended haplotypes within the HLA-DP region and survey the extent of genetic diversity in this region across human populations. In this report, we analysed single-nucleotide polymorphisms (SNPs) in 255 subjects from 6 different cohorts. The results from the HLA-DP haplotype component have validated findings from the initial pilot study. SNPs in this region were inherited in strong linkage, particularly HLA-DPA1, SNP-linked promoter haplotypes and motifs in exon 2 of HLA-DPB1. We reported 17 SNP-linked haplotypes in the promoter region. Together with HLA-DPA1 and HLA-DPB1 alleles, they formed 74 distinct extended HLA-DP haplotypes in 438 sequences. We also observed the presence of region-specific alleles and promoter haplotypes. Our approach involved phasing extended SNPs including promoter SNPs, HLA-DPA1 and HLA-DPB1 alleles, in a 22 kb region, GRCh38/hg38 (chr6:33,064,111-33,086,679), followed by clustering of these SNPs as one extended haplotype. This hierarchical clustering revealed four major clades, suggesting that haplotypes within each clade may have diverged from a common ancestral haplotype and undergone similar evolutionary processes. The correlation between HLA-DPA1 and the promoter region raises questions about the role of HLA-DPA1 antigen in the heterodimer. This finding requires validation on a larger sample size specifically designed for anthropological analysis. Nevertheless, the results from this study highlight the clinical potential of selecting better-matched donors for patients awaiting haematopoietic stem cell transplants from genetically overlapping groups that share common ancestral haplotypes.
引用
收藏
页码:690 / 706
页数:17
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