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Detection of 549 new HLA alleles in potential stem cell donors from the United States Poland and Germany

机译:在美国波兰和德国的潜在干细胞供体中检测到549个新的HLA等位基因

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摘要

We characterized 549 new human leukocyte antigen (HLA) class I and class II alleles found in newly registered stem cell donors as a result of high‐throughput HLA typing. New alleles include 101 HLA‐A, 132 HLA‐B, 105 HLA‐C, 2 HLA‐DRB1, 89 HLA‐DQB1 and 120 HLA‐DPB1 alleles. Mainly, new alleles comprised single nucleotide variations when compared with homologous sequences. We identified nonsynonymous nucleotide mutations in 70.7% of all new alleles, synonymous variations in 26.4% and nonsense substitutions in 2.9% (null alleles). Some new alleles (55, 10.0%) were found multiple times, HLA‐DPB1 alleles being the most frequent among these. Furthermore, as several new alleles were identified in individuals from ethnic minority groups, the relevance of recruiting donors belonging to such groups and the importance of ethnicity data collection in donor centers and registries is highlighted.
机译:我们对由于高通量HLA分型而在新注册的干细胞供体中发现的549种新的人白细胞抗原(HLA)I类和II类等位基因进行了表征。新的等位基因包括101 HLA-A,132 HLA-B,105 HLA-C,2 HLA-DRB1、89 HLA-DQB1和120 HLA-DPB1等位基因。与同源序列相比,新的等位基因主要包含单核苷酸变异。我们在所有新等位基因的70.7%中识别了非同义核苷酸突变,在26.4%中识别了同义变异,在2.9%中识别了无义取代(无效等位基因)。多次发现一些新的等位基因(55,10.0%),其中最常见的是HLA-DPB1等位基因。此外,由于在少数族裔群体的个体中发现了几个新的等位基因,因此强调了招募属于此类群体的捐助者的相关性以及在捐助者中心和登记处收集种族数据的重要性。

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