Enhancement of rat hepatic macrophages by treatment with interleukin-2 and streptococcal preparation OK432, with reference to antitumor activity, soluble factor production and Ia expression

Cancer Immunol Immunother. 1992;35(2):75-82. doi: 10.1007/BF01741853.

Abstract

The effect of biological response modifiers, such as interleukin-2 (IL-2) and streptococcal preparation OK432, on the functions of hepatic macrophages was investigated. The macrophages, even with no exogenous stimulation, produced superoxide anion (O2-) and tumor necrosis factor (TNF), displayed cytotoxicity against K562 cells and cytostasis against P815 cells and expressed immune-region-associated antigen (Ia). IL-2 administered in vitro or in vivo enhanced O2- production by hepatic macrophages and the intravenous injection of OK432 also enhanced O2 production. Furthermore, IL-2 added to the culture medium of hepatic macrophages isolated from OK432-injected rats augmented O2- production even more. The TNF production and Ia expression of the macrophages were also increased by the intravenous injection of OK432. As with O2- production, the cytotoxicity of the cells was enhanced by OK432 injection or by IL-2 added to the culture medium and the combination of OK432 and IL-2 augmented their cytotoxicity even more. Thus, the present study suggested that IL-2 and OK432 induce the augmentation of the antitumor activity of hepatic macrophages, partly as a result of the increase in production of O2- and TNF and Ia expression.

MeSH terms

  • Animals
  • Autoradiography
  • Carbon Radioisotopes
  • Cell Adhesion / physiology
  • Cytotoxicity, Immunologic
  • Histocompatibility Antigens Class II / physiology*
  • Humans
  • Immunologic Factors / pharmacology
  • Interleukin-2 / pharmacology*
  • Liver / cytology*
  • Liver / drug effects
  • Macrophages / drug effects*
  • Macrophages / immunology
  • Macrophages / physiology
  • Male
  • Neoplasms, Experimental / immunology
  • Neoplasms, Experimental / pathology
  • Neoplasms, Experimental / therapy*
  • Picibanil / pharmacokinetics
  • Picibanil / pharmacology*
  • Rats
  • Rats, Inbred Strains
  • Superoxides / metabolism
  • Tumor Cells, Cultured / drug effects
  • Tumor Necrosis Factor-alpha / biosynthesis

Substances

  • Carbon Radioisotopes
  • Histocompatibility Antigens Class II
  • Immunologic Factors
  • Interleukin-2
  • Tumor Necrosis Factor-alpha
  • Superoxides
  • Picibanil