CW Bill Young Marrow Donor Recruitment and Research Program, Departments of Pediatrics and Oncology, Georgetown University, Washington, District of Columbia.
Matchis Foundation, Leiden, The Netherlands.
HLA. 2019 Jun;93(6):474-483. doi: 10.1111/tan.13535. Epub 2019 Apr 4.
Next generation DNA sequencing is used to determine the HLA-A, -B, -C, -DRB1, -DRB3/4/5, and -DQB1 assignments of 1009 unrelated volunteers for the unrelated donor registry in The Netherlands. The analysis characterizes all HLA exons and introns for class I alleles; at least exons 2 to 3 for HLA-DRB1; and exons 2 to 6 for HLA-DQB1. Of the distinct alleles present, there are 229 class I and 71 class II; 36 of these alleles are novel. The majority (approximately 98%) of the cumulative allele frequency at each locus is contributed by alleles that appear three or more times. Alleles encoding protein variation outside of the antigen recognition domains are 0.6% of the class I assignments and 5.3% of the class II assignments.
下一代 DNA 测序用于确定荷兰无关供体登记处的 1009 名无关志愿者的 HLA-A、-B、-C、-DRB1、-DRB3/4/5 和 -DQB1 分配。该分析对所有 HLA 外显子和内含子进行了分类 I 等位基因的特征描述;至少对 HLA-DRB1 进行了外显子 2 到 3 的分析;对 HLA-DQB1 进行了外显子 2 到 6 的分析。在存在的独特等位基因中,有 229 个 I 类和 71 个 II 类;其中 36 个是新的。每个基因座的累积等位基因频率中,约有 98%是由出现三次或更多次的等位基因贡献的。在抗原识别结构域外编码蛋白质变异的等位基因占 I 类分配的 0.6%,占 II 类分配的 5.3%。