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胸腺在异基因造血干细胞移植中的作用。

The role of the thymus in allogeneic hematopoietic stem cell transplantation.

机构信息

Department of Biomedicine, University of Basel, and Basel University Children's Hospital (UKBB), Basel, Switzerland.

出版信息

Swiss Med Wkly. 2010 Jul 19;140:w13051. doi: 10.4414/smw.2010.13051. eCollection 2010.

Abstract

Allogeneic haematopoietic stem cell transplantation (HSCT) is used to treat an increasing number of congenital and acquired disorders of the haematopoietic system. Even though cytoreductive conditioning regimens vary in intensity, all clinically used protocols invariably cause side effects that compromise transiently or long-term the response of the natural and the adaptive immune systems. However, in the context of the reconstruction of immunity, the generation of naïve T cells constitutes a slow process, and requires a functionally competent thymus. Unfortunately, regular thymic function is frequently suppressed by transplant-related toxicities. Most notably, graft-versus-host disease (GVHD) causes a state of posttransplantation immune deficiency. Here we discuss preclinical allogeneic HSCT models and clinical observations that have contributed to a detailed understanding of the cellular and molecular mechanisms responsible for the thymic dysfunction caused by acute GVHD. An in-depth knowledge of the mechanisms that control regular thymopoiesis and, conversely, affect thymus function is expected to provide the factual basis for the design of innovative therapies to recover T-cell numbers and function following allogeneic HSCT.

摘要

异基因造血干细胞移植(HSCT)用于治疗越来越多的造血系统先天性和获得性疾病。尽管细胞减灭性预处理方案的强度不同,但所有临床应用的方案都不可避免地会导致副作用,从而暂时或长期影响天然和适应性免疫系统的反应。然而,在免疫重建的背景下,幼稚 T 细胞的产生是一个缓慢的过程,需要功能上健全的胸腺。不幸的是,常规的胸腺功能经常受到移植相关毒性的抑制。最值得注意的是,移植物抗宿主病(GVHD)导致移植后免疫缺陷状态。在这里,我们讨论了有助于详细了解急性 GVHD 引起的胸腺功能障碍的细胞和分子机制的临床前异基因 HSCT 模型和临床观察。深入了解控制正常胸腺生成的机制,以及相反地影响胸腺功能的机制,有望为设计恢复异基因 HSCT 后 T 细胞数量和功能的创新疗法提供事实基础。

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