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补体与肾移植:从供体到受体

Complement and renal transplantation: from donor to recipient.

作者信息

Damman Jeffrey, Schuurs Theo A, Ploeg Rutger J, Seelen Marc A

机构信息

Department of Surgery, University Medical Center Groningen, Groningen, The Netherlands.

出版信息

Transplantation. 2008 Apr 15;85(7):923-7. doi: 10.1097/TP.0b013e3181683cf5.

DOI:10.1097/TP.0b013e3181683cf5
PMID:18408568
Abstract

Long-term kidney graft survival is affected by different variables including donor condition, ischemia-reperfusion injury, and graft rejection during the transplantation process. The complement system is an important mediator of renal ischemia-reperfusion injury and in rejecting allografts. However, donor complement C3 seems to be crucial in renal transplantation-related injury as renal injury is attenuated in C3 deficient kidney grafts. Interestingly, before ischemia-reperfusion induced C3 expression, C3 is already induced in donors suffering from brain death. Therefore, strategies targeting complement activation in the brain-dead donor may increase graft viability and transplant outcome.

摘要

长期肾移植存活受多种因素影响,包括供体状况、缺血再灌注损伤以及移植过程中的移植物排斥反应。补体系统是肾缺血再灌注损伤和同种异体移植物排斥反应的重要介质。然而,供体补体C3似乎在肾移植相关损伤中起关键作用,因为在C3缺陷的肾移植中肾损伤会减轻。有趣的是,在缺血再灌注诱导C3表达之前,脑死亡供体中C3就已经被诱导表达。因此,针对脑死亡供体补体激活的策略可能会提高移植物的存活率和移植效果。

相似文献

1
Complement and renal transplantation: from donor to recipient.补体与肾移植:从供体到受体
Transplantation. 2008 Apr 15;85(7):923-7. doi: 10.1097/TP.0b013e3181683cf5.
2
Systemic complement activation in deceased donors is associated with acute rejection after renal transplantation in the recipient.供体系统补体激活与肾移植受者的急性排斥反应有关。
Transplantation. 2011 Jul 27;92(2):163-9. doi: 10.1097/TP.0b013e318222c9a0.
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Local renal complement C3 induction by donor brain death is associated with reduced renal allograft function after transplantation.供体脑死亡导致的局部肾脏补体 C3 诱导与移植后肾脏移植物功能降低有关。
Nephrol Dial Transplant. 2011 Jul;26(7):2345-54. doi: 10.1093/ndt/gfq717. Epub 2010 Dec 2.
4
Targeting complement activation in brain-dead donors improves renal function after transplantation.针对脑死亡供体中的补体激活可改善移植后的肾功能。
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5
Risk factors among donor characteristics which affect graft outcome in paired kidney transplantation.影响配对肾移植中移植物结局的供体特征中的危险因素。
Transplant Proc. 2008 Sep;40(7):2281-4. doi: 10.1016/j.transproceed.2008.07.105.
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Therapeutic interventions favorably influencing delayed and slow graft function in kidney transplantation: mission impossible?对肾移植中延迟和缓慢移植肾功能产生有利影响的治疗干预措施:不可能完成的任务?
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Acute but transient release of terminal complement complex after reperfusion in clinical kidney transplantation.临床肾移植再灌注后末端补体复合物的急性短暂释放。
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Contribution of renal secreted complement C3 to the circulating pool in humans.肾脏分泌的补体C3对人体循环池的贡献。
J Immunol. 1999 Apr 1;162(7):4336-41.
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Genomewide expression profiles of rat model renal isografts from brain dead donors.脑死亡供体大鼠模型肾移植的全基因组表达谱
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Impact of donor age on renal allograft function and survival.供体年龄对肾移植功能及存活的影响。
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Role of Complement System in Kidney Transplantation: Stepping From Animal Models to Clinical Application.补体系统在肾移植中的作用:从动物模型到临床应用的进展。
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Aberrant activation of the complement system in renal grafts is mediated by cold storage.
在肾脏移植物中,补体系统的异常激活是由冷储存介导的。
Am J Physiol Renal Physiol. 2021 Jun 1;320(6):F1174-F1190. doi: 10.1152/ajprenal.00670.2020. Epub 2021 May 17.
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Activation of final complement components after kidney transplantation as a marker of delayed graft function severity.肾移植后终末补体成分的激活作为移植肾功能延迟严重程度的标志物。
Clin Kidney J. 2020 Oct 10;14(4):1190-1196. doi: 10.1093/ckj/sfaa147. eCollection 2021 Apr.
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Characteristics, management and outcomes of atypical haemolytic uraemic syndrome in kidney transplant patients: a retrospective national study.肾移植患者非典型溶血尿毒综合征的特征、管理及结局:一项全国性回顾性研究
Clin Kidney J. 2020 Aug 13;14(4):1173-1180. doi: 10.1093/ckj/sfaa096. eCollection 2021 Apr.
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Role of C5aR1 and C5L2 Receptors in Ischemia-Reperfusion Injury.C5aR1和C5L2受体在缺血再灌注损伤中的作用。
J Clin Med. 2021 Mar 2;10(5):974. doi: 10.3390/jcm10050974.
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Comparative Analysis of Risk Factors in Declined Kidneys from Donation after Brain Death and Circulatory Death.脑死亡后捐献与循环死亡供肾衰竭的危险因素比较分析。
Medicina (Kaunas). 2020 Jun 26;56(6):317. doi: 10.3390/medicina56060317.
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