IL-12 or IL-15, unlike IL-2, does not interact with histamine in augmenting cytotoxicity of splenocytes against melanoma cells and YAC-1 cells

Oncol Rep. 2002 Mar-Apr;9(2):427-31.

Abstract

It has been suggested that histamine by its ability to downregulate the production of macrophage-derived reactive oxygen species might effectively potentiate the cytotoxic activity of cytokine-stimulated NK cells. Histamine thus reverses negative regulation of NK cells treated with IL-2 and IFN-alpha in the presence of macrophages. We confirm that histamine potently enhances cytotoxic activity of IL-2-stimulated NK cell-enriched splenocytes admixed with macrophages against B16F10 melanoma cells and YAC-1 cells. This stimulation results in production of high amounts of INF-gamma and TNF-alpha. Interestingly, IL-15 by itself promotes production of reactive oxygen species. Although histamine decreased reactive oxygen species production from the cultures of IL-15-stimulated NK cell-enriched splenocytes admixed with macrophages, it did not potentiate the cytotoxicity of IL-15. Further, we demonstrate that histamine-mediated potentiation of cytotoxicity is not applicable to IL-12, another potent activator of NK cell activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Survival
  • Cells, Cultured
  • Cytotoxicity, Immunologic / drug effects*
  • Drug Therapy, Combination
  • Histamine / pharmacology*
  • Humans
  • Interferon-gamma / metabolism
  • Interleukin-12 / pharmacology*
  • Interleukin-15 / pharmacology*
  • Interleukin-2 / pharmacology*
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / metabolism
  • Macrophages / metabolism
  • Melanoma, Experimental / immunology*
  • Melanoma, Experimental / metabolism
  • Melanoma, Experimental / therapy
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Peritoneum / pathology
  • Reactive Oxygen Species / metabolism
  • Spleen / cytology*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Interleukin-15
  • Interleukin-2
  • Reactive Oxygen Species
  • Tumor Necrosis Factor-alpha
  • Interleukin-12
  • Histamine
  • Interferon-gamma