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缺血/再灌注损伤中的新型细胞与分子免疫途径

New cellular and molecular immune pathways in ischemia/reperfusion injury.

作者信息

Boros P, Bromberg J S

机构信息

Recanati/Miller Transplantation Institute, The Mount Sinai School of Medicine, New York, New York, USA.

出版信息

Am J Transplant. 2006 Apr;6(4):652-8. doi: 10.1111/j.1600-6143.2005.01228.x.

Abstract

Ischemia/reperfusion injury (IRI) is a multi-factorial antigen-independent inflammatory condition that profoundly affects both early and long-term function of the allograft as suggested by both clinical and experimental data. In recent years, the acute phase of IRI has been increasingly viewed as part of the innate immune response. Identification of novel molecular pathways and new insights into the mechanisms of known mediators of IRI have established links among innate immunity, adaptive immune responses and organ regeneration, and thus long-term graft function. This review approaches these novel aspects of IRI in the context of solid organ transplantation, presenting data on new observations with kidney, liver and heart allografts.

摘要

缺血/再灌注损伤(IRI)是一种多因素、非抗原依赖性的炎症状态,临床和实验数据均表明,它会对同种异体移植物的早期和长期功能产生深远影响。近年来,IRI的急性期越来越被视为固有免疫反应的一部分。对新分子途径的识别以及对IRI已知介质机制的新见解,已在固有免疫、适应性免疫反应和器官再生之间建立了联系,进而与移植物的长期功能建立了联系。本综述在实体器官移植的背景下探讨了IRI的这些新方面,展示了关于肾、肝和心脏同种异体移植物新观察结果的数据。

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