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首页> 外文期刊>HLA. >Wide availability of HLA HLA ‐matched or a few loci‐mismatched donors in the graft‐vs‐host direction among nonsibling first‐degree relatives
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Wide availability of HLA HLA ‐matched or a few loci‐mismatched donors in the graft‐vs‐host direction among nonsibling first‐degree relatives

机译:HLA HLA-Matched或少数位于非宾至亲属之间的移植物 - 主机方向的少数位点错配的捐赠者

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摘要

Although outcomes of hematopoietic stem cell transplantation from alternative donors have been improved, it has not yet challenged the precedence of HLA‐matched or a few loci‐mismatched donors. Because the availabilities of these donors among nonsibling relatives have been scarcely discussed, we analyzed them using a large Japanese dataset of HLA typing. Data set included HLA data from 2838 patients and their relatives, distributed in all parts of Japan. Antigen mismatches at the HLA‐A, ‐B, ‐DR loci and allele mismatches at the HLA‐A, ‐B, ‐C, ‐DRB1 loci were examined. The availabilities of 0 to 1/6 antigen‐mismatched donors among one parent‐candidate and one sibling‐candidate were 24.3% and 33.9%, and those of 0 to 2/8 allele‐mismatched donors were 18.6% and 32.1%, respectively. Additional HLA‐C antigen mismatches (18.1% vs 0.0%) along with the possession of 1 to 3/8 allele mismatches (31.3% vs 3.0%) were more frequently observed in parent‐candidates than in sibling‐candidate. Most multiple allele‐mismatched pairs had HLA‐B allele mismatches. In conclusion, expanding donor searches to include nonsibling relatives could widen the availability of conventional relative donors with 0 to 1/6 antigen mismatches or 0 to 2/8 allele mismatch to 20% to 30%. High‐resolution typing including HLA‐C locus examination should be performed, because additional mismatches at HLA‐C loci along with multiple allele mismatches were often observed, especially among nonsibling pairs.
机译:尽管从替代供体的造血干细胞移植的结果得到了改善,但尚未挑战HLA匹配或几个位于偏相的供体的优先措施。因为这些捐赠者在非讨论中的可用性几乎讨论过,所以我们使用大型日本的HLA打字数据集分析它们。数据集包括来自2838名患者及其亲属的HLA数据,分布在日本的所有地区。研究了HLA-A,-B,-C,-C,-DRB1基因座的HLA-A,-B,-DR基因座和等位基因不匹配的抗原不匹配。一个母体候选和一个兄弟姐妹候选者中的0至1/6抗原非匹配供体的可用性分别为24.3%和33.9%,分别为18.6%和32.1%。在父母候选者中,额外的HLA-C抗原混合物(18.1%Vs 0.0%)与1至3/8等位基因相比,在父母候选者中比在父母候选者中更频繁地观察到(31.3%Vs 3.0%)。大多数多个等位基因不匹配的对具有HLA-B等位基因不匹配。总之,扩展捐助者搜索包括非粘性亲属可以扩大常规相对供体的可用性,以0至1/6抗原错配或0至2/8等位基因不匹配至20%至30%。应进行高分辨率打字,包括HLA-C基因座检查,因为通常观察到HLA-C LOCI的额外不匹配以及多个等位基因不匹配,特别是在非粘土对中。

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