Conversion of stable ABO‐incompatible kidney transplant recipients from mycophenolate mofetil with standard exposure calcineurin inhibitors (CNIs) to everolimus with very low exposure CNIs–a short‐term pilot study
Graft Rejection
Male
Dose-Response Relationship, Drug
Calcineurin Inhibitors
Graft Survival
Pilot Projects
Middle Aged
Mycophenolic Acid
Kidney Function Tests
Prognosis
Kidney Transplantation
ABO Blood-Group System
3. Good health
03 medical and health sciences
0302 clinical medicine
Blood Group Incompatibility
Humans
Kidney Failure, Chronic
Female
Everolimus
Immunosuppressive Agents
Follow-Up Studies
Glomerular Filtration Rate
DOI:
10.1111/ctr.12281
Publication Date:
2013-12-12T05:04:52Z
AUTHORS (9)
ABSTRACT
AbstractBackgroundA recent report has demonstrated that as with mycophenolate mofetil (MMF), everolimus is capable of inhibiting human B‐lymphocyte function and activation including B‐lymphocyte proliferation, apoptosis, and immunoglobulin production in vitro. Everolimus may therefore be used as an immunosuppressant in ABO‐incompatible kidney transplantation.MethodsA three‐month pilot study was performed to examine the efficacy and safety of conversion of stable ABO‐incompatible kidney transplant recipients from MMF with standard exposure calcineurin inhibitors (CNIs) to everolimus with very low exposure CNIs. Sixteen recipients were enrolled in the study. The patients without acute rejection by graft biopsy were switched from MMF to everolimus with CNI minimization. At three months after conversion, graft biopsies were performed to check for acute rejection and C4d deposition.ResultsConversion to everolimus with CNI minimization for three months did not induce acute rejection and C4d deposition in all of the ABO‐incompatible kidney transplant recipients. A slight elevation of anti‐A/B antibody titer occurred in our present study. Everolimus was associated with hyperlipidemia and edema.ConclusionsThese results demonstrated that short‐term conversion from MMF to everolimus after one yr post‐transplant may be a safe and effective alternate for ABO‐incompatible kidney transplant recipients requiring temporary discontinuation of MMF.
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