Preliminary in vivo pharmacokinetic and pharmacodynamic evaluation of a novel calcineurin-independent inhibitor of NFAT

Transpl Int. 2004 Mar;17(3):145-50. doi: 10.1007/s00147-003-0676-1. Epub 2004 Jan 21.

Abstract

A-285222 (A-285) is a bis-trifluoromethyl-pyrazole (BTP), a novel class of immunosuppressive agents that inhibit NFAT activity in vitro in human and non-human primate cells through a calcineurin-independent mechanism. In this preliminary study, we treated cynomolgus monkeys with different doses of A-285 for several days. Blood was collected from all animals at different times during the study. From these samples, plasma concentrations of A-285 were measured by liquid chromatography/mass spectrometry (LC/MS), and intracellular T-cell production of the cytokines IL-2, IFN-gamma, and TNF-alpha was quantified by flow cytometry using a mitogen-stimulated whole blood assay. Marked inhibition of cytokine production occurred after administration of the first dose of A-285, and this effect was comparable to that of cyclosporine. While neurological toxic side effects were seen when the plasma concentration of A-285 exceeded 4 microg/ml, at lower plasma levels the drug was well tolerated over 2 weeks and its pharmacodynamic effects were sustained throughout this time.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Animals
  • Calcineurin / physiology
  • Cytokines / biosynthesis
  • DNA-Binding Proteins
  • Macaca fascicularis
  • Male
  • NFATC Transcription Factors
  • Nuclear Proteins
  • Pyrazoles / administration & dosage
  • Pyrazoles / pharmacokinetics*
  • Pyrazoles / pharmacology
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology
  • Transcription Factors
  • Trimethylsilyl Compounds / administration & dosage
  • Trimethylsilyl Compounds / pharmacokinetics*
  • Trimethylsilyl Compounds / pharmacology

Substances

  • A 285222
  • Cytokines
  • DNA-Binding Proteins
  • NFATC Transcription Factors
  • Nuclear Proteins
  • Pyrazoles
  • Transcription Factors
  • Trimethylsilyl Compounds
  • Calcineurin