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单倍体相合造血干细胞移植治疗血液系统恶性肿瘤的进展

Advances in haploidentical stem cell transplantation for hematologic malignancies.

作者信息

Montoro Juan, Sanz Jaime, Sanz Guillermo F, Sanz Miguel A

机构信息

a Hematology Department , University Hospital La Fe and Department of Medicine, University of Valencia , Valencia , Spain.

出版信息

Leuk Lymphoma. 2016 Aug;57(8):1766-75. doi: 10.3109/10428194.2016.1167204. Epub 2016 Apr 13.

Abstract

One of the most important advances in allogeneic hematopoietic stem cell transplantation (allo-HSCT) is the use of alternative donors and cell sources, such as haploidentical transplants (haplo-HSCT) from family donors. Several approaches have been developed to overcome the challenging bidirectional alloreactivity. We discuss these approaches, including ex vivo T-cell-depleted grafts with megadose of CD34(+) cells, not requiring immunosuppression after allogeneic transplantation for graft-versus-host disease (GVHD) prophylaxis, and other strategies using unmanipulated T-cell-replete grafts with intensive immunosuppression or post-transplantation cyclophosphamide to minimize the GVHD. We also address the role of other strategies developed in the context of the haplo-HSCT platforms, such as ex vivo selective depletion of alloreactive donor T-cell subpopulations, infusion of antigen-specific T-cells against several pathogens, and infusion of regulatory T-cells, among other experimental approaches. Finally, some considerations about the selection of the most suitable donor, when more than one family member is available, are also addressed.

摘要

异基因造血干细胞移植(allo-HSCT)最重要的进展之一是使用替代供体和细胞来源,例如来自家族供体的单倍体相合移植(haplo-HSCT)。已经开发了几种方法来克服具有挑战性的双向同种异体反应性。我们讨论了这些方法,包括含有大剂量CD34(+)细胞的体外T细胞去除移植物,同种异体移植后预防移植物抗宿主病(GVHD)不需要免疫抑制,以及其他使用未处理的富含T细胞移植物并进行强化免疫抑制或移植后环磷酰胺治疗以尽量减少GVHD的策略。我们还探讨了在单倍体相合造血干细胞移植平台背景下开发的其他策略的作用,例如体外选择性去除同种异体反应性供体T细胞亚群、输注针对多种病原体的抗原特异性T细胞以及输注调节性T细胞等实验方法。最后,还讨论了在有多个家庭成员可供选择时,关于选择最合适供体的一些注意事项。

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