CNTO 530: molecular pharmacology in human UT-7EPO cells and pharmacokinetics and pharmacodynamics in mice

J Biotechnol. 2008 Mar 20;134(1-2):171-80. doi: 10.1016/j.jbiotec.2007.12.005. Epub 2007 Dec 27.

Abstract

CNTO 530 is a 58 kD antibody Fc domain fusion protein, created using Centocor's MIMETIBODY platform, that contains two EMP1 sequences as a pharmacophore. CNTO 530 has no sequence homology with EPO but acts as a novel erythropoietin receptor agonist. In UT-7(EPO) cells, CNTO 530 caused protein phosporylation of the erythropoietin receptor associated signaling pathway (Jak2, STAT5, AKT and ERK1/2). CNTO 530 also rescued these cells from apoptosis and mediated proliferation. In mice, pharmacokinetic analysis showed that CNTO 530 was slowly cleared from circulation with a t(1/2) approximately 40 h. Pharmacodynamic analysis in mice showed that a single sc dose of CNTO 530 caused a long-lived stimulation of erythropoiesis that translated into increases in red blood cell counts and hemoglobin values that were maintained for at least 28 d. In conclusion, CNTO 530 is a long-lived EPO-R agonist that stimulates erythropoiesis in a manner similar to epoetin-alpha. These data suggest that CNTO 530 may be an effective treatment of anemia in humans.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / pharmacokinetics*
  • Antibodies, Monoclonal / pharmacology*
  • Apoptosis / drug effects
  • Biological Availability
  • Bone Marrow / metabolism
  • Cell Line
  • Cell Survival / drug effects
  • Female
  • Flow Cytometry
  • Humans
  • Immunophenotyping
  • Janus Kinase 2 / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3 / metabolism
  • Models, Biological
  • Phosphorylation / drug effects
  • Receptors, Erythropoietin / agonists
  • STAT5 Transcription Factor / metabolism
  • Signal Transduction / drug effects

Substances

  • Antibodies, Monoclonal
  • Receptors, Erythropoietin
  • STAT5 Transcription Factor
  • Janus Kinase 2
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3