Review: Ischemia Reperfusion Injury-A Translational Perspective in Organ Transplantation

被引:76
作者
Fernandez, Andre Renaldo [1 ]
Sanchez-Tarjuelo, Rodrigo [2 ,3 ]
Cravedi, Paolo [4 ]
Ochando, Jordi [2 ,3 ]
Lopez-Hoyos, Marcos [1 ,5 ]
机构
[1] Univ Hosp Marques Valdecilla, Res Inst IDIVAL Santander, Immunol, Santander 390008, Spain
[2] Icahn Sch Med Mt Sinai, Dept Oncol Sci, New York, NY 10029 USA
[3] Inst Salud Carlos III, Ctr Nacl Microbiol, Immunol Trasplantes, Majadahonda 28220, Madrid, Spain
[4] Icahn Sch Med Mt Sinai, Dept Med, Div Nephrol, New York, NY 10029 USA
[5] Red Invest Renal REDINREN, Madrid 28040, Spain
关键词
ischemia reperfusion injury; cell metabolism; innate immunity; hypoxia; cell death; RNA interference; COLONY-STIMULATING FACTOR; DELAYED GRAFT FUNCTION; HEMATOPOIETIC PROGENITOR CELLS; SMALL INTERFERING RNA; G-CSF; ISCHEMIA/REPERFUSION INJURY; ALLOGRAFT-REJECTION; RAPID MOBILIZATION; SUPPRESSOR-CELLS; LIVER ISCHEMIA;
D O I
10.3390/ijms21228549
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Thanks to the development of new, more potent and selective immunosuppressive drugs together with advances in surgical techniques, organ transplantation has emerged from an experimental surgery over fifty years ago to being the treatment of choice for many end-stage organ diseases, with over 139,000 organ transplants performed worldwide in 2019. Inherent to the transplantation procedure is the fact that the donor organ is subjected to blood flow cessation and ischemia during harvesting, which is followed by preservation and reperfusion of the organ once transplanted into the recipient. Consequently, ischemia/reperfusion induces a significant injury to the graft with activation of the immune response in the recipient and deleterious effect on the graft. The purpose of this review is to discuss and shed new light on the pathways involved in ischemia/reperfusion injury (IRI) that act at different stages during the donation process, surgery, and immediate post-transplant period. Here, we present strategies that combine various treatments targeted at different mechanistic pathways during several time points to prevent graft loss secondary to the inflammation caused by IRI.
引用
收藏
页码:1 / 21
页数:21
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