Endogenous and exogenous interleukin-12 augment the protective immune response in mice orally challenged with Salmonella dublin

Infect Immun. 1996 Apr;64(4):1437-40. doi: 10.1128/iai.64.4.1437-1440.1996.

Abstract

Following oral challenge with Salmonella dublin, we observed significant increases in interleukin-12 (IL-12) protein expression in the mesenteric lymph nodes. The importance of this endogenous cytokine production in the immune response against S. dublin was demonstrated by in vivo depletion of IL-12 with an anti-IL-12 monoclonal antibody prior to oral S. dublin challenge. Mice pretreated with anti-IL-12 antibody had increased salmonellosis and reduced survival times compared with mice receiving control antibody. Furthermore, administration of exogenous murine recombinant IL-12 dramatically increased survival times of mice challenged orally with S. dublin. Together, these results demonstrate that endogenous and exogenous IL-12 significantly augment the mucosal immune response against the intracellular pathogen S. dublin.

Publication types

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

MeSH terms

  • Administration, Oral
  • Animals
  • Female
  • Interferon-gamma / biosynthesis
  • Interleukin-12 / pharmacology
  • Interleukin-12 / physiology*
  • Lipopolysaccharides / toxicity
  • Mice
  • Mice, Inbred BALB C
  • Recombinant Proteins / pharmacology
  • Salmonella Infections, Animal / immunology*

Substances

  • Lipopolysaccharides
  • Recombinant Proteins
  • Interleukin-12
  • Interferon-gamma