Donor-reactive cytokine profiles after HLA-identical living-related kidney transplantation
Nephrology, Dialysis, Transplantation , Volume 23 - Issue 6 p. 2016- 2023
Background. After HLA-identical living-related (LR) kidney transplantation, only non-HLA antigen mismatches between donor and recipient may exist. We questioned whether donor-reactive responses against non-HLA antigens could be found after HLA-identical LR kidney transplantation, and wondered whether donor reactivity in the HLA-identical setting was different from the HLA-mismatched setting during immunological quiescence. Healthy individuals served as controls. Methods. Elispot assays were performed to determine the number of alloreactive IFN-γ-producing cells (pc), IL-10 pc, granzyme B (GrB) pc and IL-13 pc from peripheral blood mononuclear cells (PBMC) of HLA-identical, HLA-mismatched LR kidney transplant recipients and healthy individuals. Results. The frequency of alloreactive IFN-γ pc, IL-13 pc and GrB pc was higher in healthy individuals compared to both transplant patient groups. In the HLA-identical group, significantly higher numbers of donor-reactive IL-10 pc were found compared to their autologous control. These frequencies were also higher compared to the HLA-mismatched and healthy control group. The number of donor-reactive GrB pc was higher in the HLA-mismatched group than in the HLA-identical group. Donor-reactive IFN-γ pc and IL-13 pc were comparable in both transplant groups. Conclusions. In recipients of HLA-identical LR kidney transplant, high donor-reactive IL-10 pc, in combination with low donor-reactive IFN-γ pc, IL-13 pc and GrB pc, suggests active downregulation of reactivity against non-HLA molecules.
|, , , , , ,|
|Nephrology, Dialysis, Transplantation|
|Organisation||Erasmus MC: University Medical Center Rotterdam|
Gerrits, J.H, van de Wetering, J, Drabbels, J.J, Claas, F.H.J, Weimar, W, & van Besouw, N.M. (2008). Donor-reactive cytokine profiles after HLA-identical living-related kidney transplantation. Nephrology, Dialysis, Transplantation, 23(6), 2016–2023. doi:10.1093/ndt/gfm899