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在国家骨髓捐赠者计划的 Be The Match 注册中心的不同种族人群中,未表达 HLA 等位基因的频率和单倍型关联。

Frequencies and haplotype associations of non-expressed HLA alleles in ethnically diverse populations on the National Marrow Donor Program's Be The Match Registry.

机构信息

National Marrow Donor Program, Minneapolis, MN, USA.

National Marrow Donor Program, Minneapolis, MN, USA.

出版信息

Hum Immunol. 2020 Oct-Nov;81(10-11):580-587. doi: 10.1016/j.humimm.2020.07.004. Epub 2020 Jul 16.

DOI:10.1016/j.humimm.2020.07.004
PMID:32684409
Abstract

HLA allele matching is critical to successful bone marrow transplantation between a patient and donor. Non-functional HLA alleles, so called 'null alleles', are not well described within a large population of well HLA-typed ethnically diverse individuals despite their impact on donor selection. A retrospective analysis was performed on 833,789 unrelated donors (URDs) in the National Marrow Donor Program's Be The Match Registry® typed for HLA-A, -B, -C, -DRB1, -DQB1, and -DPB1 by next-generation DNA sequencing. Results showed that null alleles occur in low frequency (2.30E-04) compared to expressed alleles. Their overall frequency ranged from 6.00E-07 to 9.25E-04 with a median of 1.20E-06. The expected allele associations were commonly observed for HLA-A24:09N, HLA-B51:11N, and HLA-C04:09N; however, associations outside of the expected were also observed. Notably, 82% of the National Marrow Donor Program Registry URDs carrying HLA-A24:11N showed a different HLA-C allele association, HLA-C05:01, compared to the allele described by prior published work characterizing German donor populations, HLA-C04:01. The frequencies of these observed null alleles and linkage disequilibrium information could be invaluable and helpful in guiding the HLA testing decisions.

摘要

HLA 等位基因匹配对于患者和供体之间的骨髓移植成功至关重要。尽管“无效等位基因”(所谓的“无效等位基因”)对供体选择有影响,但在大量经过良好 HLA 分型的、来自不同种族的个体中,对其进行描述并不完善。对国家骨髓捐赠者计划 Be The Match 注册中心的 833789 名无关供体(URD)进行了回顾性分析,这些供体通过下一代 DNA 测序对 HLA-A、-B、-C、-DRB1、-DQB1 和-DPB1 进行了分型。结果表明,与表达等位基因相比,无效等位基因的发生率较低(2.30E-04)。它们的总体频率范围为 6.00E-07 至 9.25E-04,中位数为 1.20E-06。常见的 HLA-A24:09N、HLA-B51:11N 和 HLA-C04:09N 存在预期的等位基因关联;然而,也观察到了超出预期的关联。值得注意的是,与先前描述德国供体群体的 HLA-A24:11N 相关的 HLA-C04:01 相比,82%的国家骨髓捐赠者计划 URD 携带 HLA-A24:11N 时具有不同的 HLA-C 等位基因关联,即 HLA-C*05:01。这些观察到的无效等位基因的频率和连锁不平衡信息可能具有重要价值,并有助于指导 HLA 测试决策。

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