The Dumont-UCLA Transplant Center, Division of Liver and Pancreas Transplantation, Department of Surgery, David Geffen School of Medicine at UCLA, 77-120 CHS, 10833 Le Conte Avenue, Los Angeles, CA 90095, USA.
Nat Rev Gastroenterol Hepatol. 2013 Feb;10(2):79-89. doi: 10.1038/nrgastro.2012.225. Epub 2012 Dec 11.
Ischaemia-reperfusion injury (IRI) in the liver, a major complication of haemorrhagic shock, resection and transplantation, is a dynamic process that involves the two interrelated phases of local ischaemic insult and inflammation-mediated reperfusion injury. This Review highlights the latest mechanistic insights into innate-adaptive immune crosstalk and cell activation cascades that lead to inflammation-mediated injury in livers stressed by ischaemia-reperfusion, discusses progress in large animal experiments and examines efforts to minimize liver IRI in patients who have received a liver transplant. The interlinked signalling pathways in multiple hepatic cell types, the IRI kinetics and positive versus negative regulatory loops at the innate-adaptive immune interface are discussed. The current gaps in our knowledge and the pathophysiology aspects of IRI in which basic and translational research is still required are stressed. An improved appreciation of cellular immune events that trigger and sustain local inflammatory responses, which are ultimately responsible for organ injury, is fundamental to developing innovative strategies for treating patients who have received a liver transplant and developed ischaemia-reperfusion inflammation and organ dysfunction.
肝脏的缺血再灌注损伤 (IRI) 是出血性休克、肝切除和肝移植的主要并发症,是一个涉及局部缺血损伤和炎症介导的再灌注损伤两个相关阶段的动态过程。本综述强调了固有免疫与适应性免疫相互作用以及导致缺血再灌注应激肝脏发生炎症介导损伤的细胞激活级联的最新机制见解,讨论了大动物实验的进展,并研究了如何减少接受肝移植患者的肝 IRI。本文讨论了多种肝实质细胞类型中的相互关联的信号通路、IRI 动力学以及固有免疫与适应性免疫界面的正、负调节环。强调了我们目前在知识上的差距以及需要进行基础和转化研究的 IRI 病理生理学方面。改善对触发和维持局部炎症反应的细胞免疫事件的认识,这些反应最终导致器官损伤,对于开发治疗接受肝移植并发生缺血再灌注炎症和器官功能障碍的患者的创新策略至关重要。