Leflunomide is a selective inhibitor of de novo
pyrimidine synthesis. In phase II and III clinical trials of active
rheumatoid arthritis,
leflunomide was shown to improve primary and secondary outcome measures with a satisfactory safety profile. The active metabolite of
leflunomide,
A77 1726, at low, therapeutically applicable doses, reversibly inhibits
dihydroorotate dehydrogenase (DHODH), the rate limiting step in the de novo synthesis of
pyrimidines. Unlike other cells, activated lymphocytes expand their
pyrimidine pool by approximately eightfold during proliferation;
purine pools are increased only twofold. To meet this demand, lymphocytes must use both salvage and de novo synthesis pathways. Thus the inhibition of DHODH by
A77 1726 prevents lymphocytes from accumulating sufficient
pyrimidines to support
DNA synthesis. At higher doses,
A77 1726 inhibits
tyrosine kinases responsible for early T cell and B cell signalling in the G(0)/G(1) phase of the cell cycle. Because the immunoregulatory effects of
A77 1726 occur at doses that inhibit DHODH but not
tyrosine kinases, the interruption of de novo
pyrimidine synthesis may be the primary mode of action. Recent evidence suggests that the observed anti-inflammatory effects of
A77 1726 may relate to its ability to suppress
interleukin 1 and tumour
necrosis factor alpha selectively over their inhibitors in T lymphocyte/monocyte contact activation.
A77 1726 has also been shown to suppress the activation of nuclear factor kappaB, a potent mediator of
inflammation when stimulated by inflammatory agents. Continuing research indicates that
A77 1726 may downregulate the glycosylation of adhesion molecules, effectively reducing cell-cell contact activation during
inflammation.