NDT Advance Access published online on November 23, 2006
Nephrology Dialysis Transplantation, doi:10.1093/ndt/gfl678
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Stable T-cell reactivity after successful tapering of azathioprine in HLA-identical living-related kidney transplant recipients despite minor histocompatibility antigen mismatches
1Department of Internal MedicineTransplantation, 2Department of Surgery, Erasmus MC, University Medical Center Rotterdam, Rotterdam and 3Department of Immunohaematology and Bloodtransfusion, Leiden University Medical Center, Leiden, The Netherlands
Correspondence and offprint requests to: Correspondence and offprint requests to: Jeroen H. Gerrits, MSc, Erasmus MC, University Medical Center Rotterdam, Department of Internal Medicine Transplantation, Room Ee-563a, P.O. Box 2040, NL-3000 CA Rotterdam, The Netherlands. Email: j.gerrits{at}erasmusmc.nl
| Abstract |
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Background. Human leukocyte antigen (HLA)-identical living-related (LR) kidney transplant recipients often receive the standard regimen of immunosuppression. We wondered whether these patients should be exposed to the side effects of these drugs any longer. Safe tapering of immunosuppression should not result in rejection and high donor-directed T-cell responses. In the present study, we investigated the effect of tapering azathioprine (AZA) on T-cell reactivity.
Methods. Fifteen HLA-identical LR kidney transplant recipients receiving a median of 150 mg/day AZA and 510 mg/day prednisone were tapered to a median of 50 mg/day AZA. Donor-, third-party reflect and tetanus toxoid (TET)-reactivity were determined in interferon (IFN)-
and interleukin (IL)-13 Elispot assays, which reflect the T-helper (Th)1 and T-helper (Th)2 response.
Results. After the tapering of AZA, none of the patients developed acute rejection and the renal function remained stable, even at 1-year follow-up. The frequency of donor-specific IFN-
and IL-13 producing cells (pc) was low. Tapering of AZA did not influence the frequency of both IFN-
and IL-13 pc. Also, the reactivity against third-party cells and TET remained unchanged.
Conclusions. The AZA-dose can be safely reduced in recipients of an HLA-identical LR kidney transplant without affecting kidney function and without increasing T-cell responses directed against donor or other antigens.
Keywords: azathioprine; interferon-
; kidney transplantation; minor histocompatibilitiy antigens; monitoring; T-cell reactivity