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HLA I类无效等位基因和新等位基因影响无关供者骨髓搜索。

HLA class I null alleles and new alleles affect unrelated bone marrow donor searches.

作者信息

Smith D M, Baker J E, Gardner W B, Martens G W, Agura E D

机构信息

Department of Pathology, Baylor University Medical Center, Dallas, TX 75246, USA. dsmith@baylor health.edu

出版信息

Tissue Antigens. 2005 Aug;66(2):93-8. doi: 10.1111/j.1399-0039.2005.00444.x.

Abstract

Unrecognized HLA null alleles or new alleles may affect the outcome of bone marrow transplants using unrelated donors. Some reports suggest that null alleles occur in the range of 0.003-0.07% (1, 2), which has led some transplant programs to stop performing serologic typing. We describe nine cases involving expression variants or new alleles. Three cases involved expression variants, including two null alleles and A24020102L. One of the null alleles was a new variant of A02. Seven cases involved new alleles. In five cases, there where discrepancies between HLA typing by serology and PCR-SSP. These included the three expression variants, one new B40 allele that typed serologically as B41 and one new B*07 allele that typed serologically as B42. Eight of these cases were found in the course of typing bone marrow transplant patients or potential unrelated donors since May of 2001 (total tested, 710 patients, 1914 donors). Thus, the incidence of null alleles was two in 2,624 (0.08%). Sequence-based typing (SBT) was performed on 676 of these samples. The decision to perform SBT was influenced by finding a serologic typing discrepancy in two cases. In one of those cases, SBT would probably have been performed at a later time, prior to final selection of a donor. Thus, the incidence of new alleles was between 4 and 6 of 676 (0.59-0.89%). We conclude that new HLA alleles and null alleles are uncommon but not extremely rare, and they continue to affect a significant number of unrelated donor searches.

摘要

未被识别的HLA无效等位基因或新等位基因可能会影响使用无关供体的骨髓移植结果。一些报告表明,无效等位基因的出现频率在0.003%-0.07%之间(1, 2),这使得一些移植项目停止进行血清学分型。我们描述了9例涉及表达变体或新等位基因的病例。3例涉及表达变体,包括2个无效等位基因和A24020102L。其中一个无效等位基因是A02的新变体。7例涉及新等位基因。在5例中,血清学HLA分型与PCR-SSP分型之间存在差异。这些包括3个表达变体、1个血清学分型为B41的新B40等位基因和1个血清学分型为B42的新B*07等位基因。自2001年5月以来,在对骨髓移植患者或潜在无关供体进行分型的过程中发现了其中8例(共检测710例患者,1914例供体)。因此,无效等位基因的发生率为2624例中有2例(0.08%)。对其中676个样本进行了基于序列的分型(SBT)。进行SBT的决定受到两例血清学分型差异的影响。在其中一例中,可能会在稍后最终选择供体之前进行SBT。因此,新等位基因的发生率为676例中有4至6例(0.59%-0.89%)。我们得出结论,新的HLA等位基因和无效等位基因并不常见,但也并非极其罕见,它们继续影响着大量无关供体的搜索。

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