Gamma interferon-independent effects of interleukin-12 on immunity to Salmonella enterica serovar typhimurium
- Author(s)
- Price, JD; Simpfendorfer, KR; Mantena, RR; Holden, J; Heath, WR; van Rooijen, N; Strugnell, RA; Wijburg, OLC;
- Details
- Publication Year 2007-12,Volume 75,Issue #12,Page 5753-5762
- Journal Title
- INFECTION AND IMMUNITY
- Publication Type
- Journal Article
- Abstract
- Interleukin-12 (IL-12) and IL-18 are both central to the induction of gamma interferon (IFN-gamma), and various roles for IL-12 and IL-18 in control of intracellular microbial infections have been demonstrated. We used IL-12p40(-/-) and IL-18(-/-) mice to further investigate the role of IL-12 and IL-18 in control of Salmonella enterica serovar Typhimurium. While C57BL/6 and IL-18-/- mice were able to resolve attenuated S. enterica serovar Typhimurium infections, the IL-12p40(-/-) mice succumbed to a high bacterial burden after 60 days. Using ovalbumin (OVA)-specific T-cell receptor transgenic T cells (OT-II cells), we demonstrated that following oral infection with recombinant S. enterica serovar Typhimurium expressing OVA, the OT-II cells proliferated in the mesenteric lymph nodes of C57BL/6 and IL-18(-/-) mice but not in IL-12p40(-/-) mice. In addition, we demonstrated by flow cytometry that equivalent or increased numbers of T cells produced IFN-gamma in IL-12p40(-/-) mice compared with the numbers of T cells that produced IFN-gamma in C57BL/6 and IL-18-/- mice. Finally, we demonstrated that removal of macrophages from S. enterica serovar Typhimurium-infected C57BL/6 and IL-12p40(-/-) mice did not affect the bacterial load, suggesting that impaired control of S. enterica serovar Typhimurium infection in the absence of IL-12p40 is not due to reduced macrophage bactericidal activities, while IL-18(-/-) mice did rely on the presence of macrophages for control of the infection. Our results suggest that IL-12p40, but not IL-18, is critical to resolution of infections with attenuated S. enterica serovar Typhimurium and that especially the effects of IL-12p40 on proliferative responses of CD4(+) T cells, but not the ability of these cells to produce IFN-gamma, are important in the resolution of infection by this intracellular bacterial pathogen.
- Publisher
- AMER SOC MICROBIOLOGY
- Keywords
- CD4(+) T-CELLS; NATURAL-KILLER-CELLS; IFN-GAMMA; IN-VIVO; ADAPTIVE IMMUNITY; ENDOGENOUS INTERLEUKIN-12; MURINE LEISHMANIASIS; STIMULATING FACTOR; HOST-RESISTANCE; CUTTING EDGE
- Publisher's Version
- https://doi.org/10.1128/IAI.00971-07
- Terms of Use/Rights Notice
- Refer to copyright notice on published article.
Creation Date: 2007-12-01 12:00:00