2025 Volume 13 Issue 1 Pages 56-60
Despite significant advances in immunosuppressive therapy, immune rejection and opportunistic infections remain major challenges in kidney transplantation. This review outlines the best practices of immunosuppressive management at Hiroshima University. A key feature is the application of CFSE-based mixed lymphocyte reaction (MLR) for individualized immune monitoring. This assay quantitatively assesses donor-reactive T-cell responses and guides optimization of immunosuppressive regimens. We also discuss the clinical utility of Everolimus (mTOR inhibitor) combined with low-dose cyclosporine, which maintains renal function while reducing CMV infections. For ABO-incompatible transplantation, our protocol incorporates rituximab-based desensitization and plasmapheresis, achieving favorable outcomes. In elderly recipients, we found that although cyclosporine doses were lower, donor-specific T-cell responses remained preserved, warranting caution in dose reduction. Additionally, analysis of patients with CMV antigenemia revealed that donor-specific T-cell immunity was unaffected despite a systemic immunosuppressive trend, challenging the routine reduction of immunosuppression during CMV infection. Overall, personalized immunosuppressive strategies using functional immune assays such as CFSE-MLR may enhance long-term graft survival in kidney transplantation.