Tumor necrosis factor is involved in the T cell-independent pathway of macrophage activation in scid mice

J Immunol. 1989 Jul 1;143(1):127-30.

Abstract

We analyzed the T cell-independent production of IFN-gamma in the severe combined immunodeficiency (scid) mutant mouse. Spleen cells from scid mice secreted high levels of IFN-gamma in response to heat-killed Listeria monocytogenes (HKLM), but not to the T cell stimulus ConA. This response was ablated by prior removal of adherent macrophages. IFN-gamma secretion in vitro was preceded by the rapid production of TNF and was inhibited by addition of neutralizing mAb to TNF. Moreover, injection of scid mice with anti-TNF mAb increased the severity of infection with live Listeria and inhibited macrophage activation for class II-MHC expression. Finally, IFN-gamma secretion and class II-MHC expression were also inhibited by an antibody to asialoGM1, a reagent known to impair host NK cell function. These results suggest that TNF is a critical cytokine in the T cell-independent pathway of macrophage activation in scid mice.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / physiology
  • Antigens, T-Independent / immunology*
  • Immunologic Deficiency Syndromes / immunology*
  • Interferon-gamma / biosynthesis
  • Killer Cells, Natural / immunology
  • Listeriosis / immunology
  • Macrophage Activation*
  • Mice
  • Mice, Mutant Strains
  • Spleen / metabolism
  • Tumor Necrosis Factor-alpha / immunology
  • Tumor Necrosis Factor-alpha / physiology*

Substances

  • Antibodies, Monoclonal
  • Antigens, T-Independent
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma