Overview
Rationale: Despite improved patient and graft survival in renal transplant recipients, still 20% of the patients reaches end-stage renal disease within 5 years after transplantation. Antibody-mediated rejection (ABMR) is one of the major causes of early graft loss and perhaps even more important of late deterioration of graft function
Objective: Evaluate the occurrence of antibody mediated rejection (ABMR) and mixed ABMR and cellular/ T-cell mediated rejection (TCMR), in patients treated with the currently prevailing immunosuppressive regimens, and relate them to outcome (graft survival, function, proteinuria, histology)
Study design: Clinical cohort study.
Study population: patients of >18 years old, about to receive a post mortal of living donor renal transplant with an immunological high risk for ABMR.
Main study parameters/endpoints: main study endpoints are the occurrence of ABMR, mixed ABMR/TCMR and renal function after 1 year of follow-up.
The main study parameter will be mapping the immune system, including B-cells, (non-)HLA antibodies, interaction between B-cells and T follicular helper cells, and complete immune profiling.
Eligibility
Inclusion Criteria:
- Kidney transplant recipients ≥18 years old
- About to receive a post mortal or living donor renal transplant
- written informed consent (is able to read of understand in Dutch)
- Immunological high risk for rejection
- Luminex positive DSAs ; or
- Retransplantation with repeated mismatch ; or
- Husband to wife donation (after fathering children); or
- Offspring to mother donation
Exclusion Criteria:
- No immunological high risk