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非恶性疾病异基因造血干细胞移植中 HLA 配型的评估。

Evaluation of HLA matching in unrelated hematopoietic stem cell transplantation for nonmalignant disorders.

机构信息

Emory University, Atlanta, GA 30322, USA.

出版信息

Blood. 2012 Oct 4;120(14):2918-24. doi: 10.1182/blood-2012-03-417758. Epub 2012 Jul 24.

Abstract

The importance of human leukocyte antigen (HLA) matching in unrelated donor transplantation for nonmalignant diseases (NMD) has yet to be defined. We analyzed data from 663 unrelated marrow and peripheral blood stem cell transplants performed from 1995 to 2007 for treatment of NMD. Transplantation from a donor mismatched at the HLA-A, -B, -C, or -DRB1, but not -DQB1 or -DPB1, loci was associated with higher mortality in multivariate analyses (P = .002). The hazard ratio for mortality for single (7/8) and double mismatched (6/8) transplants was 1.29 (0.97-1.72; P = .079) and 1.82 (1.30-2.55; P = .0004), respectively, compared with 8/8 matched transplants. HLA mismatches were not associated with acute or chronic GVHD, but were strongly associated with graft failure. After adjustment for other factors, the odds ratio for graft failure for 7/8 and 6/8 (allele and/or antigen) matched pairs compared with 8/8 matched transplants was 2.81 (1.74-4.54; P < .0001) and 2.22 (1.26-3.97; P = .006), respectively. Patients with NMD should receive transplants from allele matched (8/8) donors if possible. Unlike the case with malignancies, HLA mismatching in NMD is associated with graft failure rather than GVHD.

摘要

人类白细胞抗原(HLA)配型在非恶性疾病(NMD)的无关供体移植中的重要性尚未确定。我们分析了 1995 年至 2007 年间进行的 663 例无关骨髓和外周血干细胞移植治疗 NMD 的数据。在多变量分析中,HLA-A、-B、-C 或-DRB1 但不-DQB1 或-DPBI 位点错配的供体移植与更高的死亡率相关(P=0.002)。单(7/8)和双错配(6/8)移植的死亡风险比为 1.29(0.97-1.72;P=0.079)和 1.82(1.30-2.55;P=0.0004),而 8/8 匹配移植的风险比为 1.0。HLA 错配与急性或慢性移植物抗宿主病无关,但与移植物衰竭密切相关。在调整其他因素后,与 8/8 匹配移植相比,7/8 和 6/8(等位基因和/或抗原)匹配对的移植物衰竭的优势比分别为 2.81(1.74-4.54;P<0.0001)和 2.22(1.26-3.97;P=0.006)。如果可能的话,NMD 患者应接受等位基因匹配(8/8)供体的移植。与恶性肿瘤不同,NMD 中的 HLA 错配与移植物衰竭相关,而不是与移植物抗宿主病相关。

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