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T-cell activation and transplantation tolerance.T 细胞活化与移植耐受。
Transplant Rev (Orlando). 2012 Jul;26(3):212-22. doi: 10.1016/j.trre.2011.09.002. Epub 2011 Nov 8.
2
Modulating T-cell costimulation as new immunosuppressive concept in organ transplantation.调节 T 细胞共刺激作为器官移植中的新型免疫抑制概念。
Curr Opin Organ Transplant. 2012 Aug;17(4):368-75. doi: 10.1097/MOT.0b013e328355fc94.
3
Induction of transplantation tolerance to fully mismatched cardiac allografts by T cell mediated delivery of alloantigen.通过 T 细胞介导的同种异体抗原传递诱导完全错配心脏移植物的移植耐受。
Clin Immunol. 2010 Aug;136(2):174-87. doi: 10.1016/j.clim.2010.04.012. Epub 2010 May 8.
4
Role of innate immunity in transplantation tolerance.天然免疫在移植耐受中的作用。
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5
Memory T-cell exhaustion and tolerance in transplantation.移植中的记忆 T 细胞耗竭与耐受。
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T-cell costimulatory pathways in allograft rejection and tolerance.同种异体移植排斥与耐受中的T细胞共刺激途径。
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7
Costimulation blockade: current perspectives and implications for therapy.协同刺激阻断:当前的观点及其对治疗的影响。
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Tolerance--is it worth it?宽容——这值得吗?
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Costimulatory molecules as targets for the induction of transplantation tolerance.共刺激分子作为诱导移植耐受的靶点。
Curr Mol Med. 2006 Dec;6(8):843-57. doi: 10.2174/156652406779010812.

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Desensitization in HLA-incompatible kidney transplant recipients: current strategies and emerging perspectives.HLA不相合肾移植受者的脱敏治疗:当前策略与新观点
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J Brown Hosp Med. 2024 Jul 1;3(3):118963. doi: 10.56305/001c.118963. eCollection 2024.
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Exploring Costimulatory Blockade-Based Immunologic Strategies in Transplantation: Are They a Promising Immunomodulatory Approach for Organ and Vascularized Composite Allotransplantation?探索基于共刺激阻断的移植免疫策略:它们是器官和血管化复合异体移植有前景的免疫调节方法吗?
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Human PD-L1 overexpression decreases xenogeneic human T-cell immune responses towards porcine kidneys.人 PD-L1 的过表达降低了异种人 T 细胞对猪肾脏的免疫反应。
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Manipulation of Regulatory Dendritic Cells for Induction Transplantation Tolerance.调控树突状细胞诱导移植耐受的研究进展
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Bendamustine with total body irradiation conditioning yields tolerant T-cells while preserving T-cell-dependent graft-versus-leukemia.苯达莫司汀联合全身照射预处理可产生耐受性T细胞,同时保留T细胞依赖性移植物抗白血病效应。
Oncoimmunology. 2020 Apr 30;9(1):1758011. doi: 10.1080/2162402X.2020.1758011. eCollection 2020.
8
Impact of infection on transplantation tolerance.感染对移植耐受的影响。
Immunol Rev. 2019 Nov;292(1):243-263. doi: 10.1111/imr.12803. Epub 2019 Sep 19.
9
CCR4 expression on host T cells is a driver for alloreactive responses and lung rejection.宿主 T 细胞上的 CCR4 表达是同种反应性应答和肺排斥反应的驱动因素。
JCI Insight. 2019 May 14;5(12):121782. doi: 10.1172/jci.insight.121782.
10
In vivo reprogramming of immune cells: Technologies for induction of antigen-specific tolerance.免疫细胞的体内重编程:诱导抗原特异性耐受的技术
Adv Drug Deliv Rev. 2017 May 15;114:240-255. doi: 10.1016/j.addr.2017.04.005. Epub 2017 Apr 14.

本文引用的文献

1
Pillars article: CTLA-4 can function as a negative regulator of T cell activation. Immunity. 1994. 1: 405-413.支柱文章:细胞毒性T淋巴细胞相关抗原4(CTLA-4)可作为T细胞活化的负调节因子。《免疫》杂志。1994年。第1卷:405 - 413页。
J Immunol. 2011 Oct 1;187(7):3466-74.
2
CD40-specific costimulation blockade enhances neonatal porcine islet survival in nonhuman primates.CD40 特异性共刺激阻断增强了非人类灵长类动物新生猪胰岛的存活。
Am J Transplant. 2011 May;11(5):947-57. doi: 10.1111/j.1600-6143.2011.03509.x.
3
Bacterial infections, alloimmunity, and transplantation tolerance.细菌感染、同种免疫和移植耐受。
Transplant Rev (Orlando). 2011 Jan;25(1):27-35. doi: 10.1016/j.trre.2010.10.003.
4
Ex vivo-expanded human regulatory T cells prevent the rejection of skin allografts in a humanized mouse model.体外扩增的人调节性 T 细胞可预防人源化小鼠模型中皮肤同种异体移植物的排斥反应。
Transplantation. 2010 Dec 27;90(12):1321-7. doi: 10.1097/TP.0b013e3181ff8772.
5
B cells help alloreactive T cells differentiate into memory T cells.B 细胞帮助同种反应性 T 细胞分化为记忆 T 细胞。
Am J Transplant. 2010 Sep;10(9):1970-80. doi: 10.1111/j.1600-6143.2010.03223.x.
6
Allografts stimulate cross-reactive virus-specific memory CD8 T cells with private specificity.同种异体移植物刺激具有个体特异性的交叉反应性病毒特异性记忆 CD8 T 细胞。
Am J Transplant. 2010 Aug;10(8):1738-48. doi: 10.1111/j.1600-6143.2010.03161.x.
7
Infection with the intracellular bacterium, Listeria monocytogenes, overrides established tolerance in a mouse cardiac allograft model.胞内细菌李斯特菌感染使小鼠心脏移植模型中已建立的耐受状态被破坏。
Am J Transplant. 2010 Jul;10(7):1524-33. doi: 10.1111/j.1600-6143.2010.03066.x.
8
IFN-alpha beta and self-MHC divert CD8 T cells into a distinct differentiation pathway characterized by rapid acquisition of effector functions.IFN-αβ 和自身 MHC 将 CD8 T 细胞导入一个具有特征性的分化途径,该途径表现为快速获得效应功能。
J Immunol. 2010 Aug 1;185(3):1419-28. doi: 10.4049/jimmunol.1001140. Epub 2010 Jun 30.
9
Potential T regulatory cell therapy in transplantation: how far have we come and how far can we go?移植中的潜在调节性 T 细胞治疗:我们已经走了多远,还能走多远?
Transpl Int. 2010 Aug;23(8):761-70. doi: 10.1111/j.1432-2277.2010.01127.x. Epub 2010 Jun 11.
10
In vivo prevention of transplant arteriosclerosis by ex vivo-expanded human regulatory T cells.体外扩增的人调节性 T 细胞预防移植动脉硬化。
Nat Med. 2010 Jul;16(7):809-13. doi: 10.1038/nm.2154. Epub 2010 May 16.

T 细胞活化与移植耐受。

T-cell activation and transplantation tolerance.

机构信息

Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.

出版信息

Transplant Rev (Orlando). 2012 Jul;26(3):212-22. doi: 10.1016/j.trre.2011.09.002. Epub 2011 Nov 8.

DOI:10.1016/j.trre.2011.09.002
PMID:22074786
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3294261/
Abstract

Transplantation of allogeneic or "nonself" tissues stimulates a robust immune response leading to graft rejection, and therefore, most recipients of allogeneic organ transplants require the lifelong use of immune suppressive agents. Excellent outcomes notwithstanding, contemporary immunosuppressive medications are toxic, are often not taken by patients, and pose long-term risks of infection and malignancy. The ultimate goal in transplantation is to develop new treatments that will supplant the need for general immunosuppression. Here, we will describe the development and application of costimulation blockade to induce transplantation tolerance and discuss how the diverse array of signals that act on T cells will determine the balance between graft survival and rejection.

摘要

同种异体或“非自体”组织移植会刺激强烈的免疫反应,导致移植物排斥,因此,大多数接受同种异体器官移植的患者需要终身使用免疫抑制剂。尽管取得了优异的效果,但目前的免疫抑制剂具有毒性,且经常不被患者使用,长期存在感染和恶性肿瘤的风险。移植的最终目标是开发新的治疗方法,以取代对全身免疫抑制的需求。在这里,我们将描述共刺激阻断的发展和应用,以诱导移植耐受,并讨论作用于 T 细胞的各种信号将如何决定移植物存活和排斥之间的平衡。