SRS301 - Subnormothermic machine perfusion of human kidneys using an acellular perfusion solution is non-inferior to red blood cell based perfusion

Harry Spiers(NHS Blood and Transplant), Sarah Hosgood(NHS Blood and Transplant), Sara Deffrennes(KU Leuven), Serena MacMillan(NHS Blood and Transplant), Miguel Larraz(NHS Blood and Transplant), Mia Freishem(NHS Blood and Transplant), Anna Paterson(Cambridge University Hospitals NHS Foundation Trust), Irina Mohorianu(University of Southampton), Michael Nicholson(NHS Blood and Transplant), Vasilis Kosmoliaptsis(NHS Blood and Transplant)
British journal of surgery
March 1, 2026
Cited by 0

Abstract

Abstract Background Normothermic machine perfusion (NMP) preserves kidneys in a near-physiological state, allowing viability assessment and intervention. NMP typically uses red blood cell (RBC)-based perfusates, with associated challenges, including blood type compatibility, haemolysis, and free haem–driven ferroptotic tubular injury. Acellular perfusates avoid these risks. Subnormothermic machine perfusion (SMP, 32°C) may reduce metabolic demands while preserving organ viability, but the effect of perfusate type under these conditions remains unclear. Methods In a paired experimental design, kidneys from eight deceased donors were randomized 1:1 to 6 h of SMP with RBC-based (RBC-SMP) or acellular perfusate (SNAP), followed by 4 h of RBC-based NMP (37°C) to simulate reperfusion. Bulk RNA sequencing, transcriptomic pathway scoring, urinary biomarkers, and histology were used to compare perfusion methods. Publicly available RBC-NMP transcriptomic data were integrated for comparison. Results Transcriptional comparison showed no difference in pathways related to ischaemia-reperfusion injury (IRI; TNFα via NFκB, Allograft Rejection, Inflammatory Response) and Oxidative Phosphorylation, at 6 h SMP and 4 h reperfusion between RBC-SMP and SNAP kidneys. Similarly, metabolism-associated transcriptional pathways, urinary tubular injury biomarkers (NGAL, L-FABP, TIMP2, IGFBP7), and histological injury were similar between groups. Compared to 6 h of RBC-NMP at 37°C, both subnormothermic groups showed less depletion of oxidative phosphorylation with similar IRI levels, suggesting preserved mitochondrial function. Conclusions Acellular subnormothermic kidney perfusion is equivalent to RBC-based SMP at the transcriptomic, metabolic, and tubular injury level. Our data support the clinical feasibility of SNAP as a safe, logistically simple alternative for kidney preservation.


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