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Q J Med 2000; 93: 15-20
© 2000 Association of Physicians


Reviews

The evolving role of mycophenolate mofetil in renal transplantation

A.N. Warrens

From the Division of Medicine, Imperial College School of Medicine, London, UK

Dr A.N. Warrens, Renal Unit, Imperial College School of Medicine, Hammersmith Hospital, L Block, Du Cane Road, London W12 0HS. e-mail: a.warrens@ic.ac.uk


    Pharmacology
 
Mycophenolate mofetil (MMF) is an ester prodrug with higher bioavailability than the active agent, mycophenolic acid (MPA).1 MPA inhibits inosine monophosphate (IMP) dehydrogenase, an enzyme that facilitates the conversion of IMP to xanthosine monophosphate, a precursor of guanine nucleotides. This is an important step in the de novo pathway of purine nucleotide synthesis on which lymphocytes primarily depend, unlike neutrophils, for example.2 In addition, different isoforms of IMP dehydrogenase exist, and MPA is not only almost five times more potent in inhibiting the type II isoform, that is associated with stimulated rather than resting lymphocytes,3 but is also, to some extent, cell type specific.4 Thus, on theoretical grounds, MMF represents a significant improvement on the antimetabolite azathioprine the use of which is well-established in organ transplantation.


    In vitro and animal studies
 
MMF is effective in prolonging the survival of mouse and rat cardiac allografts,5,6 showing an additive effect with cyclosporin, brequinar or tacrolimus.6–9 It can . . . [Full Text of this Article]


    Clinical experience in renal transplantation
 
Prophylaxis
Rescue therapy
Maintenance therapy

    Significance of the effect of MMF on the incidence of acute rejection
 

    Adverse effects
 

    Conclusions
 

    References
 

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