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在异基因造血干细胞移植中,区分移植物抗白血病与移植物抗宿主病。

Separating graft-versus-leukemia from graft-versus-host disease in allogeneic hematopoietic stem cell transplantation.

机构信息

Department of Hematology/Oncology, Emory University School of Medicine, Winship Cancer Institute, 1365C Clifton Road NE, Room C4002, Atlanta, GA 3032, USA.

出版信息

Immunotherapy. 2009 Jul;1(4):599-621. doi: 10.2217/imt.09.32.

Abstract

Routine methods to maximize the graft-versus-leukemia (GvL) activity of allogeneic hematopoietic stem cell transplantation (HSCT) without the detrimental effects of graft-versus-host disease (GvHD) are lacking. Depletion or inhibition of alloreactive T cells is partially effective in preventing GvHD, but usually leads to decreased GvL activity. The current model for the pathophysiology of acute GvHD describes a series of immune pathways that lead to activation of donor T cells and inflammatory cytokines responsible for tissue damage in acute GvHD. This model does not account for how allotransplant can lead to GvL effects without GvHD, or how the initial activation of donor immune cells may lead to counter-regulatory effects that limit GvHD. In this review, we will summarize new findings that support a more complex model for the initiation of GvHD and GvL activities in allogeneic HSCT, and discuss the potential of novel strategies to enhance GvL activity of the transplant.

摘要

常规方法旨在最大限度地提高异基因造血干细胞移植(HSCT)的移植物抗白血病(GvL)活性,而又不产生移植物抗宿主病(GvHD)的有害作用。缺乏耗竭或抑制同种异体反应性 T 细胞的方法,部分有效预防 GvHD,但通常会导致 GvL 活性降低。目前关于急性 GvHD 的病理生理学模型描述了一系列免疫途径,导致供体 T 细胞和炎症细胞因子的激活,从而导致急性 GvHD 中的组织损伤。该模型不能解释为什么同种异体移植可以在没有 GvHD 的情况下产生 GvL 效应,也不能解释供体免疫细胞的初始激活如何导致限制 GvHD 的代偿性效应。在这篇综述中,我们将总结新的发现,这些发现支持了一个更复杂的模型,用于启动异基因 HSCT 中的 GvHD 和 GvL 活性,并讨论增强移植的 GvL 活性的新策略的潜力。

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