No effect of remote ischaemic conditioning on inflammation in a porcine kidney transplantation model

作者:Secher Niels*; Soendergaard Peter; Ravlo Kristian; Soelling Christoffer; Granfeldt Asger; Wogensen Lise; Keller Anna K; Moeldrup Ulla; Ostraat Ernst O; Joergensen Troels M; Jespersen Bente; Toennesen Else
来源:Transplant Immunology, 2014, 31(2): 98-104.
DOI:10.1016/j.trim.2014.05.005

摘要

Main problem: Delayed graft function after kidney transplantation is associated with decreased graft survival and increased patient mortality but the pathogenesis is poorly understood. Remote ischaemic conditioning (rIC) may prevent delayed graft function by an anti-inflammatory effect. In a porcine model of transplantation from adults to children, we investigated the inflammatory response in the transplanted kidney and the effect of rIC. Methods: Kidneys were recovered from brain dead donor pigs(63 kg) and transplanted into two groups of recipient pigs(15 kg) after 22 h of cold ischaemia. Recipients were randomised to either: rIC (n = 8) performed before the 10-h reperfusion period or no-rIC (n = 8). Non-transplanted kidneys from eight brain dead pigs served as controls. Results: Compared to controls, transplantation increased the number of apoptotic cells, macrophages and neutrophils in the kidney. After transplantation, IL-10 levels increased and IL-6 levels decreased in the kidney, whereas levels of TNF-alpha and IL-8 were not affected. A significant rise in plasma IL-1 beta and IL-6 was observed in the recipients after transplantation. Plasma IL-10 was not affected by transplantation and TNF-alpha and IL-8 were below detection limit. No effect of rIC was found with regards to cell infiltration or cytokine production. Conclusion: Renal transplantation elicits an inflammatory response in the kidney manifested as apoptotic cell death, macrophage and neutrophil infiltration, and an anti-inflammatory cytokine response 10 h after transplantation. This response was not modified by rIC.

  • 出版日期2014-8