Chronic-active antibody-mediated rejection with or without donor-specific antibodies has similar histomorphology and clinical outcome
A retrospective study
Chronic-active antibody-mediated rejection (c-aABMR) is defined as histological evidence of chronic endothelial injury (cg), also known as transplant glomerulopathy, and either microvascular inflammation (MVI) or positivity for C4d. Importantly, the presence of donor-specific antibodies (DSA) is currently still mandatory for the diagnosis of c-aABMR. This retrospective study of 41 c-aABMR patients investigates whether cases suspicious for c-aABMR (DSA negative, n = 24) differ from cases of c-aABMR (DSA positive, n = 17) with respect to renal histology, allograft function and long-term graft survival. All included patients had progressive loss of allograft function and were diagnosed by for cause biopsy and scored according to the Banff '15 criteria. In all DSApos cases, DSA were de novo and the majority was directed against HLA-II being mostly anti-HLA-DQ antibodies. There were no statistically significant differences in clinical characteristics, decline in allograft function and renal allograft survival in cases with or without DSAs. All cases showed chronic histomorphological damage and inflammation, irrespective of the presence of DSA. Renal histology and clinical outcome of patients suspicious for c-aABMR (DSAneg) do not significantly differ from patients with a diagnosis of c-aABMR (DSApos). We believe that our study adds to the ongoing debate regarding the need for DSAs to be present for the diagnosis of c-aABMR.
|Keywords||Histocompatibility and immunogenetics, HLA-antibody posttransplantation, Kidney clinical, Rejection|
|Persistent URL||dx.doi.org/10.1111/tri.13154, hdl.handle.net/1765/105814|
Sablik, K.A, Clahsen-van Groningen, M.C, Looman, C.W.N, Damman, J, Roelen, D.L, Agteren, M, & Betjes, M.G.H. (2018). Chronic-active antibody-mediated rejection with or without donor-specific antibodies has similar histomorphology and clinical outcome. Transplant International. doi:10.1111/tri.13154