Immunopharmacology of recombinant human interleukin-18 in non-human primates

Cytokine. 2002 Oct 7;20(1):38-48. doi: 10.1006/cyto.2002.1978.

Abstract

Recombinant human interleukin (IL)-18 (rHuIL-18) has a potential as a therapeutic agent in cancer and is currently in drug development. Since human IL-18 displays 96% and 100% amino acid sequence homology with cynomolgus monkey and chimpanzee IL-18, respectively, the biological responses to rHuIL-18 were evaluated in these species. A single intravenous dose of rHuIL-18 at 1 or 10mg/kg in cymonolgus monkeys caused a transient reduction in lymphocyte counts, induction of IL-1alpha and tumour necrosis factor alpha (TNF-alpha) mRNA in whole blood cells and a marked increase in plasma neopterin. rHuIL-18 administered to cynomolgus monkeys at doses of 0.3 or 3mg/kg for two 5-day cycles (Days 1-5 and 15-19) resulted in increased monocyte counts, induction of NK cells and concomitant increases in plasma IL-12 and neopterin. Administration of repeat doses of rHuIL-18 at 10mg/kg to chimpanzees was associated with increased monocyte counts, upregulation of FcgammaRI surface expression on monocytes, and increased IL-8, IL-12 and neopterin in plasma. These studies demonstrate, for the first time, the immunostimulatory activity of rHuIL-18 in vivo. The described pharmacological profile of rHuIL-18 in both cynomolgus monkeys and chimpanzees is indicative of the immunotherapeutic potential of rHuIL-18 in the treatment of cancer.

MeSH terms

  • Animals
  • Cytokines / metabolism
  • Humans
  • Interleukin-18 / administration & dosage
  • Interleukin-18 / pharmacology*
  • Macaca fascicularis
  • Monocytes / drug effects
  • Monocytes / immunology
  • Neopterin / biosynthesis
  • Pan troglodytes
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / pharmacology
  • T-Lymphocyte Subsets
  • Tachyphylaxis

Substances

  • Cytokines
  • Interleukin-18
  • Recombinant Proteins
  • Neopterin