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Journal Article | Research Support, U.S. Gov't, P.H.S.

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

T Kincy-Cain, J D Clements, K L Bost
T Kincy-Cain
Department of Microbiology and Immunology, Tulane University Medical Center, New Orleans, Louisiana 70112-2699, USA.
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J D Clements
Department of Microbiology and Immunology, Tulane University Medical Center, New Orleans, Louisiana 70112-2699, USA.
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K L Bost
Department of Microbiology and Immunology, Tulane University Medical Center, New Orleans, Louisiana 70112-2699, USA.
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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.

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Endogenous and exogenous interleukin-12 augment the protective immune response in mice orally challenged with Salmonella dublin.
T Kincy-Cain, J D Clements, K L Bost
Infection and Immunity Apr 1996, 64 (4) 1437-1440; DOI:

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Endogenous and exogenous interleukin-12 augment the protective immune response in mice orally challenged with Salmonella dublin.
T Kincy-Cain, J D Clements, K L Bost
Infection and Immunity Apr 1996, 64 (4) 1437-1440; DOI:
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