Modelling acute antibody-mediated rejection of human kidney transplants using ex-vivo warm machine perfusion

• Published in: EBioMedicine Vol. 86; p. 104365
• Main Authors: Chandak, Pankaj, Phillips, Benedict L., Bennett, Danothy, Uwechue, Raphael, Kessaris, Nicos, Shaw, Olivia, Maggs, Tim, Woodford, Luke, Veniard, David, Perera, Ranmith, Parmar, Kiran, Hunt, Beverley J., Callaghan, Chris, Dorling, Anthony, Mamode, Nizam
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.12.2022; Elsevier
• Subjects: ABO Blood-Group System; Antibodies; Antibody-mediated rejection; Ex-vivo normothermic perfusion; Graft Rejection; HLA Antigens; HLA/ABO incompatible transplantation; Human kidney transplant model; Humans; Kidney - pathology; Kidney Transplantation - adverse effects; Perfusion; Ex-vivo normothermic perfusion; Antibody-mediated rejection; Human kidney transplant model; HLA/ABO incompatible transplantation
• ISSN: 2352-3964; 2352-3964
• DOI: 10.1016/j.ebiom.2022.104365

Transplant rejection is a major cause of graft loss and morbidity. Currently, no human models of antibody-mediated rejection (AMR) exist, limiting mechanistic investigation and organ-specific targeted therapy. Here, using 12 human kidneys and ex-vivo normothermic machine perfusion, we demonstrate phenotypes of AMR after addition of antibodies against either human HLA class I or blood group antigens (A, B), thus modelling clinical AMR that can follow HLA incompatible (HLAi) or blood group incompatible (ABOi) transplantation. Discarded human kidneys with wide ranging demographics and cold ischaemia times (11–54 h) were perfused with red blood cells and fresh frozen plasma (FFP) as a source of complement/coagulation factors. For the HLAi model, 600 μg of W6/32 anti-class 1 HLA antibody was added to the circuit (time '0'). For the ABOi model, high titre FFP of the relevant blood group antibody was added. Renal blood flow index (RBFi, mL/min/100 g), C3 desArg, prothrombin fragments 1 + 2 and histology were determined. Our endpoints included haemodynamic changes, thrombosis, and biopsy proven complement deposition. Compared to control kidneys perfused without anti-donor antibodies, both models demonstrated haemodynamic collapse after antibody perfusion with only the HLAi model showing glomerular C4d deposition. We show that a clinically relevant human kidney model of AMR is feasible, and anticipate that these models, with refinements, could provide a basis to test different strategies to prevent AMR. The Rosetrees and Stonygate Trust, The Royal College of Surgeons of England Fellowship Grant, NIHR Biomedical Research Centre/KCL Early Career Grant, Kidney Research U.K.