Granulocyte-macrophage colony-stimulating factor potentiates antitumor activity of interleukin-12 in melanoma model in mice

Tumour Biol. 1998;19(2):77-87. doi: 10.1159/000029978.

Abstract

To study the antitumor activity of the combination immunotherapy with interleukin-12 (IL-12) and granulocyte-macrophage colony-stimulating factor (GM-CSF), a murine MmB 16 melanoma tumor model was used. Seven days after inoculation of MmB 16 melanoma cells into the footpad of the right hind limb, mice were treated with IL-12 and/or GM-CSF administered intratumorally for 7 consecutive days. IL-12 used both at a high (1 microg) and at a low (0.01 microg) dose per day produced retardation of tumor growth, although neither treatment resulted in any significant prolongation of the survival of tumor-bearing mice. GM-CSF did not by itself exert antitumor activity in this model; however, it potentiated antitumor effects of IL-12. In particular, survival of tumor-bearing mice treated with IL-12 (0.01 microg per day) and GM-CSF was significantly prolonged compared with that in mice treated with either IL-12 or GM-CSF alone.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Division
  • Cell Survival
  • Drug Synergism
  • Erythrocyte Count / drug effects
  • Granulocyte-Macrophage Colony-Stimulating Factor / therapeutic use*
  • Hindlimb
  • Interleukin-12 / therapeutic use*
  • Leukocyte Count / drug effects
  • Macrophages, Peritoneal / drug effects
  • Macrophages, Peritoneal / physiology
  • Melanoma, Experimental / blood
  • Melanoma, Experimental / pathology
  • Melanoma, Experimental / therapy*
  • Mice
  • Nitric Oxide / biosynthesis
  • Organ Size / drug effects
  • Platelet Count / drug effects
  • Recombinant Proteins / therapeutic use
  • Spleen / drug effects
  • Time Factors

Substances

  • Recombinant Proteins
  • Interleukin-12
  • Nitric Oxide
  • Granulocyte-Macrophage Colony-Stimulating Factor