Highly biased type 1 immune responses in mice deficient in LFA-1 in Listeria monocytogenes infection are caused by elevated IL-12 production by granulocytes

J Immunol. 2003 Oct 15;171(8):3970-6. doi: 10.4049/jimmunol.171.8.3970.

Abstract

LFA-1 (CD11a/CD18) plays a key role in various inflammatory responses. Here we show that the acquired immune response to Listeria monocytogenes is highly biased toward type 1 in the absence of LFA-1. At the early stage of listeriosis, numbers of IFN-gamma producers in the liver and spleen of LFA-1(-/-) mice were markedly increased compared with heterozygous littermates and Valpha14(+)NKT cell-deficient mice, and NK cells were major IFN-gamma producers. Numbers of IL-12 producers were also markedly elevated in LFA-1(-/-) mice compared with heterozygous littermates, and endogenous IL-12 neutralization impaired IFN-gamma production by NK cells. Granulocyte depletion diminished numbers of IL-12 producers and IFN-gamma-secreting NK cells in the liver of LFA-1(-/-) mice. Granulocytes from the liver of L. monocytogenes-infected LFA-1(-/-) mice were potent IL-12 producers. Thus, in the absence of LFA-1, granulocytes are a major source of IL-12 at the early stage of listeriosis. We assume that highly biased type 1 immune responses in LFA-1(-/-) mice are caused by increased levels of IL-12 from granulocytes and that granulocytes play a major role in IFN-gamma secretion by NK cells. In conclusion, LFA-1 regulates type 1 immune responses by controlling prompt infiltration of IL-12-producing granulocytes into sites of inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / administration & dosage
  • Cell Movement / genetics
  • Cell Movement / immunology
  • Granulocytes / immunology*
  • Granulocytes / metabolism
  • Granulocytes / pathology
  • Immunity, Active / genetics
  • Immunity, Innate / genetics
  • Injections, Intraperitoneal
  • Interferon-gamma / antagonists & inhibitors
  • Interferon-gamma / biosynthesis
  • Interferon-gamma / metabolism
  • Interleukin-12 / antagonists & inhibitors
  • Interleukin-12 / biosynthesis*
  • Interleukin-12 / immunology
  • Interleukin-12 / physiology
  • Killer Cells, Natural / immunology
  • Killer Cells, Natural / metabolism
  • Listeria monocytogenes / immunology
  • Listeriosis / genetics*
  • Listeriosis / immunology*
  • Listeriosis / metabolism
  • Liver / immunology
  • Liver / metabolism
  • Liver / pathology
  • Lymphocyte Function-Associated Antigen-1 / biosynthesis
  • Lymphocyte Function-Associated Antigen-1 / genetics*
  • Lymphocyte Function-Associated Antigen-1 / physiology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Up-Regulation / genetics
  • Up-Regulation / immunology*

Substances

  • Antibodies, Monoclonal
  • Lymphocyte Function-Associated Antigen-1
  • Interleukin-12
  • Interferon-gamma