泰国自愿干细胞供体人白细胞抗原-A、-B、-C、-DRB1、-DQB1和-DPB1高分辨率分型的等位基因和单倍型频率

IF 3.6 3区 医学 Q2 HEMATOLOGY
Sriprapai Khanuntong, Tamonwan Tupmongkol, Sirilak Phiancharoen, Apiwat Tiyapan, Pawinee Kupatawintu, Dootchai Chaiwanichsiri, Martin Maiers, Pimol Chiewsilp
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引用次数: 0

摘要

HLA等位基因和单倍型频率计算来自110,007名HLA高分辨率分型自愿供者和280,998名HLA中至高分辨率分型自愿供者。这是首次在泰国人群中进行高分辨率HLA分型的大样本研究。HLA-A、-B、-C、-DRB1、-DQB1和-DPB1等位基因和单倍型的频率通过下一代测序(NGS)分型计算。HLA-A、-B、-C、-DRB1、-DQB1和-DPB1的G组总数分别为44、83、38、42、16和39个。HLA-A、-B、-C、-DRB1、-DQB1和-DPB1双野单等位基因总数分别为142个、196个、122个、122个、71个和124个。泰国人HLA等位基因的多样性占IMGT/HLA数据库总等位基因的1.86% ~ 5.58%。HLA-A、-B、-C、-DRB1、-DQB1和-DPB1共有、中间和充分记录(CIWD)组等位基因频率分别为104、155、87、98、48和96。频率大于5%的等位基因分别为A*02:03、A*11:01、A*33:03、A*02:07、A*24:02、A*24:07、B*46:01、B*15:02、B*44:03、C*01:02、C*07:02、C*03:04、C*08:01、DRB1*12:02、DRB1*14:54和DQB1*03:03。频率大于10%的单倍型分别是A*33:03 ~ C*03:02 ~ B*58:01 ~ DRB1*03:01 ~ DQB1*02:01、A*02:07 ~ C*01:02 ~ B*46:01 ~ DRB1*09:01 ~ DQB1*03:03、A*33:03 ~ C*07:01:01G ~ B*44:03 ~ DRB1*07:01 ~ DQB1*02:01:01G和A*11:01 ~ C*08:01 ~ B*15:02 ~ DRB1*12:02 ~ DQB1*03:01。这些发现使登记处能够预测为罕见HLA分型患者找到良好匹配的器官和干细胞供体的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Allele and Haplotype Frequencies in High-Resolution Typing of Human Leukocyte Antigen -A, -B, -C, -DRB1, -DQB1 and -DPB1 in Thai Voluntary Stem Cell Donors.

The HLA allele and haplotype frequencies were calculated from 110,007 voluntary donors with HLA high-resolution typing and 263,542 voluntary donors with medium to high-resolution typing. This is the first study of a large samples with high-resolution HLA typing in Thai population. The frequencies of HLA-A, -B, -C, -DRB1, -DQB1 and -DPB1 alleles and haplotypes were calculated from typing by next generation sequencing (NGS). A total number of G groups for HLA-A, -B, -C, -DRB1, -DQB1 and -DPB1 were 44, 83, 38, 42, 16 and 39, respectively. A total number of 2-field single allele for HLA-A, -B, -C, -DRB1, -DQB1 and -DPB1 were 142, 196, 122, 122, 71, and 124, respectively. The variety of each HLA alleles in the Thais ranging from 1.86% to 5.58% of the total alleles in IMGT/HLA database. The frequencies of allele following common, intermediate and well-documented (CIWD) groups for HLA-A, -B, -C, -DRB1, -DQB1 and -DPB1 were 104, 155, 87, 98, 48 and 96, respectively. The alleles with frequency greater than 5% were A*02:03, A*11:01, A*33:03, A*02:07, A*24:02, A*24:07, B*46:01, B*15:02, B*44:03, C*01:02, C*07:02, C*03:04, C*08:01, DRB1*12:02, DRB1*14:54 and DQB1*03:03. The haplotypes with frequency greater than 10% were A*33:03∼C*03:02∼B*58:01∼DRB1*03:01∼DQB1*02:01, A*02:07∼C*01:02∼B*46:01∼DRB1*09:01∼DQB1*03:03,A*33:03∼C*07:01:01G∼B*44:03∼DRB1*07:01∼DQB1*02:01:01G and A*11:01∼C*08:01∼ B*15:02∼DRB1*12:02∼ DQB1*03:01. These findings enable the registry to predict the opportunity to find good matched organ and stem cell donors for the patient with rare HLA typing.

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