Nephrol Dial Transplant (2001) 16: 1752-1756
© 2001 European Renal Association-European Dialysis and Transplant Association
Editorial Comments
Mycophenolate mofetil: implications for the treatment of glomerular disease
1 Département de Néphrologie et EA645, Université Claude Bernard, Hopital Edouard Herriot, Lyon and 2 GREF, Université Victor Segalen Bordeaux 2, Bordeaux, France
Keywords: inflammatory glomerular disease; mycophenolate mofetil
Introduction
Mycophenolate mofetil (MMF) is a specific inhibitor of inosine monophosphate dehydrogenase, which is involved in de novo purine synthesis. MMF is a suppressor of both T and B cell lymphocyte proliferation [1,2] and has been used successfully for the prevention of acute and chronic rejection of renal allografts [3,4]. MMF is more effective than azathioprine in preventing acute rejection. Interestingly, although MMF has been introduced as an immunosuppressive drug, it has also effects on non-immune cells. In particular it has an antiproliferative action on vascular smooth muscle cells [5,6] and this may be responsible, at least in part, for the beneficial effect of MMF on chronic graft dysfunction [7].
Only limited information is available with respect to the use of MMF for the treatment of autoimmune diseases. There are experimental studies documenting that MMF inhibits the
Mechanisms of action and pharmacokinetics
Action of mycophenolate on specific cell functions
Selective inhibition of lymphocyte functions
Deoxyguanosine nucleotide depletion
Effects on non-immune cells
Mycophenolate mofetil and experimental models of glomerular disease
Mycophenolate mofetil in human glomerular disease
MMF and recurrent glomerulonephritis in allografts
Mycophenolate mofetil and primary glomerular diseases
Mycophenolate mofetil and lupus nephritis
Mycophenolate mofetil and vasculitis
Nephrotic syndrome
IgA nephropathy
Conclusions
Acknowledgments
Notes
References
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