Tim-3 signaling pathway as a novel negative mediator in lipopolysaccharide-induced endotoxic shock

Hum Immunol. 2014 May;75(5):470-8. doi: 10.1016/j.humimm.2014.02.001. Epub 2014 Feb 20.

Abstract

Sepsis is a complex clinical condition caused by a dysregulated immune response to an infection. However, the mechanism by which our immune system controls this amplified inflammation is largely unknown. In this study, we investigated whether Tim-3 pathway could serve as a negative mediator in lipopolysaccharide (LPS)-induced endotoxic shock. Our results showed that Tim-3 was expressed on CD4(+) T cells, CD8(+) T cells, and NK cells, and was significantly increased in the peritoneal cavity of septic mice. Tim-3 acted as a marker of immune exhaustion and Tim-3-positive T cells and NK cells had a lower interferon (IFN)-γ production. Furthermore, blockade of Tim-3 pathway significantly accelerated mortality in septic mice, while activation of this pathway prolonged survival time. In vitro administration of Tim-3 blocking antibody restored the release of IFN-γ from splenocytes and decreased splenocyte apoptosis, and increased levels of IFN-γ and tumor necrosis factor (TNF)-α were also detected in septic mice at 24h post in vivo administration of the antibody. In contrast, activation of Tim-3 pathway prevented cell proliferation. Thus, Tim-3 signaling pathway acts as a novel negative mediator in LPS-induced endotoxic shock and could be a potential therapeutic target for the treatment of sepsis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / pharmacology
  • Disease Models, Animal
  • Galectins / biosynthesis
  • Galectins / pharmacology
  • Hepatitis A Virus Cellular Receptor 2
  • Interferon-alpha / biosynthesis
  • Interferon-gamma / biosynthesis
  • Killer Cells, Natural / immunology
  • Killer Cells, Natural / metabolism
  • Lipopolysaccharides / immunology
  • Male
  • Mice
  • Receptors, Virus / antagonists & inhibitors
  • Receptors, Virus / metabolism*
  • Shock, Septic / immunology
  • Shock, Septic / metabolism*
  • Shock, Septic / mortality
  • Signal Transduction* / drug effects
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism

Substances

  • Antibodies, Monoclonal
  • Galectins
  • Havcr2 protein, mouse
  • Hepatitis A Virus Cellular Receptor 2
  • Interferon-alpha
  • Lipopolysaccharides
  • Receptors, Virus
  • galectin 9, mouse
  • Interferon-gamma