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共刺激分子作为诱导移植耐受的靶点。

Costimulatory molecules as targets for the induction of transplantation tolerance.

作者信息

Alegre Maria-Luisa, Najafian Nader

机构信息

Department of Medicine, The University of Chicago, Chicago, IL 60637, USA.

出版信息

Curr Mol Med. 2006 Dec;6(8):843-57. doi: 10.2174/156652406779010812.

Abstract

Transplantation is the only cure for end-stage organ failure. Transplanted tissues are usually recognized by the immune system as foreign and are rapidly rejected in the absence of immunosuppression. Transplanted organs between genetically distinct individuals are termed allografts and their acute rejection is orchestrated by the activation of allospecific T cells. To prevent acute allograft rejection, current therapies suppress all T cells irrespective of their specificities and must be taken life-long, leaving patients with decreased defenses against infectious agents and cancers. The goal in transplantation research is to develop therapies with the capacity to induce graft-specific tolerance. Ideal therapies should be of short duration and target only alloreactive T cells, leaving other T cells competent to fight infections and cancers. Researchers have studied the mechanisms of activation/regulation of T cells in the hopes that manipulation of these pathways may facilitate the induction of tolerance. Activation of T cells requires recognition by the T cell receptor (TCR) of antigenic peptides presented within major histocompatibility complexes (MHC) on the surface of antigen-presenting cells (APCs). In addition, concurrent engagement of costimulatory receptors on T cells by ligands on APCs is also required for optimal T cell responses, such that the ultimate outcome of TCR engagement reflects the relative sum of multiple positive and negative costimulatory signals. Targeting costimulatory receptor/ligand pairs has been used effectively to induce allograft tolerance in specific rodent transplantation models. This strategy has however been less effective in larger mammals. In this review, we will summarize the different reagents used to target costimulatory molecules, their effects, and the possible reasons limiting their efficacy in higher order mammals.

摘要

移植是终末期器官衰竭的唯一治愈方法。移植的组织通常会被免疫系统识别为外来物,在没有免疫抑制的情况下会迅速被排斥。基因不同个体之间移植的器官称为同种异体移植物,其急性排斥反应是由同种特异性T细胞的激活所介导的。为了防止急性同种异体移植物排斥反应,目前的治疗方法会抑制所有T细胞,而不考虑其特异性,并且必须终身服用,这使得患者对感染因子和癌症的防御能力下降。移植研究的目标是开发能够诱导移植物特异性耐受的治疗方法。理想的治疗方法应该持续时间短,并且只针对同种异体反应性T细胞,使其他T细胞能够有效抵抗感染和癌症。研究人员研究了T细胞激活/调节的机制,希望通过操纵这些途径来促进耐受的诱导。T细胞的激活需要T细胞受体(TCR)识别抗原呈递细胞(APC)表面主要组织相容性复合体(MHC)中呈递的抗原肽。此外,APC上的配体与T细胞上共刺激受体的同时结合也是最佳T细胞反应所必需的,因此TCR结合的最终结果反映了多个正性和负性共刺激信号的相对总和。在特定的啮齿动物移植模型中,靶向共刺激受体/配体对已被有效地用于诱导同种异体移植物耐受。然而,这一策略在大型哺乳动物中效果较差。在这篇综述中,我们将总结用于靶向共刺激分子的不同试剂、它们的作用以及限制其在高等哺乳动物中疗效的可能原因。

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