Neutralization of IL-18 reduces neutrophil tissue accumulation and protects mice against lethal Escherichia coli and Salmonella typhimurium endotoxemia

J Immunol. 2000 Mar 1;164(5):2644-9. doi: 10.4049/jimmunol.164.5.2644.

Abstract

In addition to stimulating IFN-gamma synthesis, IL-18 also possesses inflammatory effects by inducing synthesis of the proinflammatory cytokines TNF and IL-1beta and the chemokines IL-8 and macrophage inflammatory protein-1alpha. We hypothesized that neutralization of IL-18 would have a beneficial effect in lethal endotoxemia in mice. IL-1beta converting enzyme (ICE)-deficient mice, lacking the ability to process mature IL-18 and IL-1beta, were completely resistant to lethal endotoxemia induced by LPS derived from either Escherichia coli or Salmonella typhimurium. In contrast, both wild-type and IL-1beta-/- mice were equally susceptible to the lethal effects of LPS, implicating that absence of mature IL-18 or IFN-gamma but not IL-1beta in ICE-/- mice is responsible for this resistance. However, IFN-gamma-deficient mice were not resistant to S. typhimurium LPS, suggesting an IFN-gamma-independent role for IL-18. Anti-IL-18 Abs protected mice against a lethal injection of either LPS. Anti-IL-18 treatment also reduced neutrophil accumulation in liver and lungs. The increased survival was accompanied by decreased levels of IFN-gamma and macrophage inflammatory protein-2 in anti-IL-18-treated animals challenged with E. coli LPS, whereas IFN-gamma and TNF concentrations were decreased in treated mice challenged with S. typhimurium. In conclusion, neutralization of IL-18 during lethal endotoxemia protects mice against lethal effects of LPS. This protection is partly mediated through inhibition of IFN-gamma production, but mechanisms involving decreased neutrophil-mediated tissue damage due to the reduction of either chemokines (E. coli LPS) or TNF (S. typhimurium LPS) synthesis by anti-IL-18 treatment may also be involved.

Publication types

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

MeSH terms

  • Animals
  • Cell Movement / immunology*
  • Chemokines / biosynthesis
  • Endotoxemia / immunology*
  • Endotoxemia / mortality
  • Endotoxemia / pathology
  • Endotoxemia / prevention & control
  • Escherichia coli Infections / immunology*
  • Escherichia coli Infections / mortality
  • Escherichia coli Infections / pathology
  • Escherichia coli Infections / prevention & control
  • Immune Sera / pharmacology*
  • Injections, Intraperitoneal
  • Interferon-gamma / antagonists & inhibitors
  • Interferon-gamma / biosynthesis
  • Interleukin-18 / antagonists & inhibitors
  • Interleukin-18 / biosynthesis
  • Interleukin-18 / immunology*
  • Lipopolysaccharides / administration & dosage
  • Liver / enzymology
  • Liver / immunology
  • Liver / metabolism
  • Lung / enzymology
  • Lung / immunology
  • Lung / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Neutrophils / immunology*
  • Neutrophils / pathology
  • Peroxidase / metabolism
  • Salmonella Infections, Animal / immunology*
  • Salmonella Infections, Animal / mortality
  • Salmonella Infections, Animal / pathology
  • Salmonella Infections, Animal / prevention & control
  • Salmonella typhimurium / immunology*
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / biosynthesis

Substances

  • Chemokines
  • Immune Sera
  • Interleukin-18
  • Lipopolysaccharides
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma
  • Peroxidase