Wagner J E, Rosenthal J, Sweetman R, Shu X O, Davies S M, Ramsay N K, McGlave P B, Sender L, Cairo M S
Department of Pediatrics, University of Minnesota School of Medicine, Minneapolis 55455, USA.
Blood. 1996 Aug 1;88(3):795-802.
To reduce the morbidity and mortality associated with unrelated donor bone marrow (BM) transplantation and potentially extend the pool of suitable donors, cryopreserved unrelated donor umbilical cord blood was considered as an alternate source of hematopoietic stem cells for transplantation. Patients with leukemia, BM failure syndrome, or inborn error of metabolism were eligible for a phase I clinical trial designed to estimate the risk of graft failure and severe acute graft-versus-host disease after transplantation of umbilical cord blood from unrelated donors. As of December 21, 1995, unrelated donor umbilical cord blood was used to reconstitute hematopoiesis in eighteen patients aged 0.1 to 21.3 years weighing 3.3 to 78.8 kg with acquired or congenital lympho-hematopoietic disorders or metabolic disease. Patients received either HLA-matched (n = 7) or HLA-1 to 3 antigen disparate (n = 11) grafts collected and evaluated by the New York Blood Center (New York, NY). The probability of engraftment after unrelated donor umbilical cord blood transplantation was 100% with no patient having late graft failure to date. The probability of grade III-IV acute graft-versus-host disease at 100 days was 11%. With a median follow-up of 6 months (range, 1.6 to 17 months); the probability of survival at 6 months is 65% in this high risk patient population. We conclude that cryopreserved umbilical cord blood from HLA-matched and mismatched unrelated donors is a sufficient source of transplantable hematopoietic stem cells with high probability of donor derived engraftment and low risk of refractory severe acute graft-versus-host disease. Limitations with regard to recipient size and degree of donor HLA disparity remain to be determined.
为降低与非血缘供者骨髓移植相关的发病率和死亡率,并有可能扩大合适供者的范围,冷冻保存的非血缘供者脐带血被视为移植造血干细胞的替代来源。患有白血病、骨髓衰竭综合征或先天性代谢缺陷的患者符合一项I期临床试验的条件,该试验旨在评估非血缘供者脐带血移植后移植物失败和严重急性移植物抗宿主病的风险。截至1995年12月21日,非血缘供者脐带血已用于18例年龄在0.1至21.3岁、体重3.3至78.8kg、患有获得性或先天性淋巴造血系统疾病或代谢性疾病的患者的造血重建。患者接受了由纽约血液中心(纽约,纽约)采集和评估的HLA匹配(n = 7)或HLA 1至3个抗原不相合(n = 11)的移植物。非血缘供者脐带血移植后的植入概率为100%,迄今为止没有患者出现晚期移植物失败。100天时III-IV级急性移植物抗宿主病的概率为11%。中位随访时间为6个月(范围1.6至17个月);在这个高风险患者群体中,6个月时的生存概率为65%。我们得出结论,来自HLA匹配和不相配的非血缘供者的冷冻保存脐带血是可移植造血干细胞的充足来源,供者来源植入的可能性高,难治性严重急性移植物抗宿主病的风险低。关于受者大小和供者HLA不相合程度的局限性仍有待确定。