Abstract

Abstract We tested here the effects of malononitrilamide (MNA) 279 and MNA 715 (derivatives of A771726, the active metabolite of leflunomide) in monotherapy and in combination with cyclosporine A (CSA) on heterotopically transplanted rat cardiac allografts (BN) [Brown Norway Lewis]. Both MNAs (5–20 mg/kg) displayed a dose-dependent increase of efficacy. The combination of CSA (5 mg/kg) with the MNAs (5 and 10 mg/kg) showed a synergistic effect in the prolongation of allograft survival and in the induction of long-term allograft survival. To investigate the immunological mechanism responsible for long-term allograft survival, we transplanted second set (BN) and third party (Dark Agouti) skin allografts on the tail of long-term surviving rats. The cause for long-term allograft survival turned out to be a donor-specific tolerance. We formulate a hypothesis for the mechanism of the synergism of the combination MNA + CSA in the induction of tolerance.

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