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主要组织相容性复合体同种异体识别途径。

Pathways of major histocompatibility complex allorecognition.

机构信息

Department of Nephrology and Transplantation, Guy's Hospital, Kings College London, London, UK.

出版信息

Curr Opin Organ Transplant. 2008 Aug;13(4):438-44. doi: 10.1097/MOT.0b013e328309ee31.

Abstract

PURPOSE OF REVIEW

Here, we review the pathways of allorecognition and their potential relevance to the balance between regulatory and effector responses following transplantation.

RECENT FINDINGS

Transplantation between nonidentical members of the same species elicits an immune response that manifests as graft rejection or persistence. Presentation of foreign antigen to recipient T cells can occur via three nonmutually exclusive routes, the direct, indirect and semi-direct pathways. Allospecific T cells can have effector or regulatory functions, and the relative proportions of the two populations activated following alloantigen presentation are two of the factors that determine the clinical outcome. Regulatory T cells have been the subject of significant research, and there is now greater understanding of their recruitment and function in the context of allorecognition.

SUMMARY

A greater understanding of the mechanisms underlying allorecognition may be fundamental to appreciating how these different populations are recruited and could in turn inform novel strategies for immunomodulation.

摘要

目的综述

在此,我们综述了同种异体识别的途径及其与移植后调节和效应反应之间平衡的潜在相关性。

最近的发现

同一物种的非同一成员之间的移植会引发免疫反应,表现为移植物排斥或持续存在。供体 T 细胞对外来抗原的呈递可以通过三种非相互排斥的途径发生,即直接途径、间接途径和半直接途径。同种异体特异性 T 细胞可以具有效应或调节功能,在同种抗原呈递后激活的两种群体的相对比例是决定临床结果的两个因素之一。调节性 T 细胞一直是大量研究的主题,现在人们对其在同种异体识别中的募集和功能有了更深入的了解。

总结

对同种异体识别的潜在机制的理解可能是理解这些不同群体如何被招募的基础,反过来也可以为免疫调节提供新的策略。

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