T-cell costimulatory molecules in acute-graft-versus host disease: therapeutic implications.

Bone Marrow Research Pub Date : 2011-01-01 Epub Date: 2010-09-21 DOI:10.1155/2011/976793
Javier Briones, Silvana Novelli, Jorge Sierra
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引用次数: 53

Abstract

Acute Graft-versus-host disease (GVHD) is a major complication after allogeneic hematopoietic stem cell transplantation. Although this process is thought to consist of several phases, T-cell activation plays a critical role in the pathogenesis of acute GVHD. To become efficient effectors, T-cells require additional costimulation after T-cell receptor signaling. A number of molecules are involved in costimulation of T-cells such as CD28, CD40L, CD30, OX40, 4-1BB, ICOS, and LIGHT. The system is regulated by inhibitory molecules, CTLA-4, and PD-1. There is experimental evidence that those molecules are implicated in the pathogenesis of GHVD. We describe how these molecules are involved in acute GVHD and how the blockade of costimulatory molecules may have potential implications for the treatment of patients with acute GVHD.
急性移植物抗宿主病中的t细胞共刺激分子:治疗意义。
急性移植物抗宿主病(GVHD)是同种异体造血干细胞移植后的主要并发症。尽管这一过程被认为包括几个阶段,但t细胞激活在急性GVHD的发病机制中起着关键作用。为了成为有效的效应器,t细胞在t细胞受体信号传递后需要额外的共刺激。许多分子参与t细胞的共刺激,如CD28、CD40L、CD30、OX40、4-1BB、ICOS和LIGHT。该系统受抑制分子CTLA-4和PD-1的调控。有实验证据表明这些分子与GHVD的发病机制有关。我们描述了这些分子是如何参与急性GVHD的,以及如何阻断共刺激分子可能对急性GVHD患者的治疗有潜在的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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