Cutting edge: cross-regulation by TLR4 and T cell Ig mucin-3 determines sex differences in inflammatory heart disease

J Immunol. 2007 Jun 1;178(11):6710-4. doi: 10.4049/jimmunol.178.11.6710.

Abstract

Recent clinical studies have reinforced the importance of sex-related differences in the pathogenesis of cardiovascular diseases, with an increased incidence and mortality in men. Similar to humans, male BALB/c mice infected with coxsackievirus B3 (CVB3) develop more severe inflammation in the heart even though viral replication is no greater than in females. We show that TLR4 and IFN-gamma levels are significantly elevated and regulatory T cell (Treg) populations significantly reduced in the heart of males following CVB3 infection, whereas females have significantly increased T cell Ig mucin (Tim)-3, IL-4 and Treg. Blocking Tim-3 in males significantly increases inflammation and TLR4 expression while reducing Treg. In contrast, defective TLR4 signaling significantly reduces inflammation while increasing Tim-3 expression. Cross-regulation of TLR4 and Tim-3 occurs during the innate and adaptive immune response. This novel mechanism may help explain why inflammatory heart disease is more severe in males.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Coxsackievirus Infections / immunology
  • Coxsackievirus Infections / metabolism
  • Coxsackievirus Infections / physiopathology
  • Enterovirus B, Human / immunology
  • Female
  • Hepatitis A Virus Cellular Receptor 2
  • Macrophages / immunology
  • Macrophages / metabolism
  • Male
  • Mast Cells / immunology
  • Mast Cells / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • Mice, Transgenic
  • Myocarditis / immunology*
  • Myocarditis / metabolism
  • Myocarditis / physiopathology*
  • Myocarditis / virology
  • Receptor Cross-Talk / immunology*
  • Receptors, Virus / antagonists & inhibitors
  • Receptors, Virus / biosynthesis
  • Receptors, Virus / physiology*
  • Sex Characteristics*
  • Signal Transduction / immunology
  • Toll-Like Receptor 4 / antagonists & inhibitors
  • Toll-Like Receptor 4 / biosynthesis
  • Toll-Like Receptor 4 / physiology*
  • Up-Regulation / immunology

Substances

  • Havcr2 protein, mouse
  • Hepatitis A Virus Cellular Receptor 2
  • Receptors, Virus
  • Toll-Like Receptor 4