Krenger Werner, Holländer Georg A
Department of Biomedicine, University of Basel, Basel, 4005, Switzerland.
Semin Immunopathol. 2008 Dec;30(4):439-56. doi: 10.1007/s00281-008-0131-6. Epub 2008 Oct 31.
The clinical success of allogeneic hematopoietic stem cell transplantation (HSCT) depends on the appropriate reconstitution of the host's immune system. While recovery of T-cell immunity may occur in transplant recipients via both thymus-dependent and thymus-independent pathways, the regeneration of a population of phenotypically naive T cells with a broad receptor repertoire relies entirely on the de novo generation of T-cells in the thymus. Preclinical models and clinical studies of allogeneic HSCT have identified the thymus as a target of graft-versus-host disease (GVHD), thus limiting T-cell regeneration. The present review focuses on recent insight into how GVHD affects thymic structure and function and how this knowledge may aid in the design of new strategies to improve T-cell reconstitution following allogeneic HSCT.
异基因造血干细胞移植(HSCT)的临床成功取决于宿主免疫系统的适当重建。虽然移植受者的T细胞免疫可通过胸腺依赖性和非胸腺依赖性途径恢复,但具有广泛受体库的表型幼稚T细胞群体的再生完全依赖于胸腺中T细胞的从头生成。异基因HSCT的临床前模型和临床研究已将胸腺确定为移植物抗宿主病(GVHD)的靶标,从而限制了T细胞的再生。本综述重点关注GVHD如何影响胸腺结构和功能的最新见解,以及这些知识如何有助于设计新策略以改善异基因HSCT后的T细胞重建。