Department of Medicine, University Hospitals Case Medical Center, Case Western Reserve University, Cleveland, OH 44106.
Mediterr J Hematol Infect Dis. 2010;2(3):e2010033. doi: 10.4084/MJHID.2010.033. Epub 2010 Nov 3.
Allogeneic hematopoietic cell transplantation (HCT) represents a vital procedure for patients with various hematologic conditions. Despite advances in the field, HCT carries significant morbidity and mortality. A rare but potentially devastating complication is transplantation-associated thrombotic microangiopathy (TA-TMA). In contrast to idiopathic TTP, whose etiology is attributed to deficient activity of ADAMTS13, (a member of the A Disintegrin And Metalloprotease with Thrombospondin 1 repeats family of metalloproteases), patients with TA-TMA have > 5% ADAMTS13 activity. Pathophysiologic mechanisms associated with TA-TMA, include loss of endothelial cell integrity induced by intensive conditioning regimens, immunosuppressive therapy, irradiation, infections and graft-versus-host (GVHD) disease. The reported incidence of TA-TMA ranges from 0.5% to 75%, reflecting the difficulty of accurate diagnosis in these patients. Two different groups have proposed consensus definitions for TA-TMA, yet they fail to distinguish the primary syndrome from secondary causes such as infections or medication exposure. Despite treatment, mortality rate in TA-TMA ranges between 60% to 90%. The treatment strategies for TA-TMA remain challenging. Calcineurin inhibitors should be discontinued and replaced with alternative immunosuppressive agents. Daclizumab, a humanized monoclonal anti-CD25 antibody, has shown promising results in the treatment of TA-TMA. Rituximab or the addition of defibrotide, have been reported to induce remission in this patient population. In general, plasma exchange is not recommended.
异基因造血细胞移植(HCT)是治疗各种血液系统疾病患者的重要手段。尽管该领域取得了进展,但 HCT 仍存在较高的发病率和死亡率。一种罕见但潜在破坏性的并发症是移植相关血栓性微血管病(TA-TMA)。与特发性 TTP 不同,后者的病因归因于 ADAMTS13 活性缺乏(ADAMTS13,一种解整合素和金属蛋白酶与血小板反应蛋白 1 重复家族的金属蛋白酶),TA-TMA 患者的 ADAMTS13 活性>5%。与 TA-TMA 相关的病理生理机制包括强化预处理方案、免疫抑制治疗、辐射、感染和移植物抗宿主病(GVHD)引起的内皮细胞完整性丧失。TA-TMA 的报告发病率为 0.5%至 75%,反映了这些患者准确诊断的困难。有两个不同的小组提出了 TA-TMA 的共识定义,但它们未能区分原发性综合征与感染或药物暴露等继发性原因。尽管进行了治疗,TA-TMA 的死亡率仍在 60%至 90%之间。TA-TMA 的治疗策略仍然具有挑战性。应停用钙调神经磷酸酶抑制剂,并改用替代免疫抑制剂。人源化单克隆抗 CD25 抗体达利珠单抗在治疗 TA-TMA 方面显示出良好的效果。利妥昔单抗或添加去纤维蛋白原,已被报道可诱导该患者群体缓解。一般不建议进行血浆置换。