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同种异体移植排斥与耐受中的细胞外囊泡。

Extracellular vesicles in allograft rejection and tolerance.

机构信息

Center for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.

Center for Transplantation Sciences, Department of Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.

出版信息

Cell Immunol. 2020 Mar;349:104063. doi: 10.1016/j.cellimm.2020.104063. Epub 2020 Feb 8.

DOI:10.1016/j.cellimm.2020.104063
PMID:32087929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7231511/
Abstract

Extracellular vesicles (EVs), including exosomes, ectosomes and apoptotic vesicles, play an essential role in communication between cells of the innate and adaptive immune systems. Recent studies showed that EVs released after transplantation of allogeneic tissues and organs are involved in the immune recognition and response leading to rejection or tolerance in mice. After skin, pancreatic islet, and solid organ transplantation, donor-derived EVs were shown to initiate direct inflammatory alloresponses by T cells leading to acute rejection. This occurred through presentation of intact allogeneic MHC molecules on recipient antigen presenting cells (MHC cross-dressing) and subsequent activation of T cells via semi-direct allorecognition. On the other hand, some studies have documented the role of EVs in maternal tolerance of fetal alloantigens during pregnancy and immune privilege associated with spontaneous tolerance of liver allografts in laboratory rodents. The precise nature of the EVs, which are involved in rejection or tolerance, and the cells which produce them, is still unclear. Nevertheless, several reports showed that EVs released in the blood and urine by allografts can be used as biomarkers of rejection. This article reviews current knowledge on the contribution of EVs in allorecognition by T cells and discusses some mechanisms underlying their influence on T cell alloimmunity in allograft rejection or tolerance.

摘要

细胞外囊泡(EVs),包括外泌体、ectosomes 和凋亡小体,在固有免疫和适应性免疫系统细胞之间的通讯中发挥着重要作用。最近的研究表明,同种异体组织和器官移植后释放的 EVs 参与了免疫识别和反应,导致小鼠排斥或耐受。在皮肤、胰岛和实体器官移植后,供体来源的 EVs 被证明通过 T 细胞引发直接炎症同种异体反应,导致急性排斥。这是通过在受者抗原呈递细胞上呈现完整的同种异体 MHC 分子(MHC 交叉染色),并通过半直接同种异体识别随后激活 T 细胞来实现的。另一方面,一些研究记录了 EVs 在怀孕期间母体对胎儿同种异体抗原的耐受以及与实验室啮齿动物肝脏同种异体移植自发耐受相关的免疫特权中的作用。参与排斥或耐受的 EVs 以及产生它们的细胞的确切性质仍不清楚。然而,有几项报道表明,同种异体移植物在血液和尿液中释放的 EVs 可用作排斥的生物标志物。本文综述了 EVs 在 T 细胞同种异体识别中的作用的最新知识,并讨论了它们对同种异体移植排斥或耐受中 T 细胞同种免疫的影响的一些机制。

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本文引用的文献

1
Expression Profiling of Exosomal miRNAs Derived from the Peripheral Blood of Kidney Recipients with DGF Using High-Throughput Sequencing.采用高通量测序技术对 DGF 肾移植受者外周血来源的外泌体 miRNA 进行表达谱分析。
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Novel urinary exosomal biomarkers of acute T cell-mediated rejection in kidney transplant recipients: A cross-sectional study.新型尿液外泌体生物标志物在肾移植受者急性 T 细胞介导排斥反应中的应用:一项横断面研究。
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Circulating Exosomes with Distinct Properties during Chronic Lung Allograft Rejection.慢性肺移植排斥反应过程中具有不同特性的循环外泌体。
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Graft-infiltrating PD-L1 cross-dressed dendritic cells regulate antidonor T cell responses in mouse liver transplant tolerance.嵌合浸润 PD-L1 的树突状细胞调节小鼠肝移植耐受中的抗供体 T 细胞反应。
Hepatology. 2018 Apr;67(4):1499-1515. doi: 10.1002/hep.29529. Epub 2018 Feb 18.
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Extracellular vesicles derived from T regulatory cells suppress T cell proliferation and prolong allograft survival.调节性 T 细胞来源的细胞外囊泡抑制 T 细胞增殖并延长移植物存活时间。
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Serum exosomal protein profiling for the non-invasive detection of cardiac allograft rejection.血清外泌体蛋白质谱分析用于心脏移植排斥的非侵入性检测。
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Plasma Exosomes From HLA-Sensitized Kidney Transplant Recipients Contain mRNA Transcripts Which Predict Development of Antibody-Mediated Rejection.来自HLA致敏肾移植受者的血浆外泌体含有可预测抗体介导排斥反应发生的mRNA转录本。
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Modification of host dendritic cells by microchimerism-derived extracellular vesicles generates split tolerance.微嵌合来源的细胞外囊泡对宿主树突状细胞的修饰产生了分裂耐受。
Proc Natl Acad Sci U S A. 2017 Jan 31;114(5):1099-1104. doi: 10.1073/pnas.1618364114. Epub 2017 Jan 17.