Histamine H(1) receptor signaling regulates effector T cell responses and susceptibility to coxsackievirus B3-induced myocarditis

Cell Immunol. 2012;272(2):269-74. doi: 10.1016/j.cellimm.2011.10.004. Epub 2011 Oct 15.

Abstract

Susceptibility to autoimmune myocarditis has been associated with histamine release by mast cells during the innate immune response to coxsackievirus B3 (CVB3) infection. To investigate the contribution of histamine H(1) receptor (H(1)R) signaling to CVB3-induced myocarditis, we assessed susceptibility to the disease in C57BL/6J (B6) H(1)R(-/-) mice. No difference was observed in mortality between CVB3-infected B6 and H(1)R(-/-) mice. However, analysis of their hearts revealed a significant increase in myocarditis in H(1)R(-/-) mice that is not attributed to increased virus replication. Enhanced myocarditis susceptibility correlated with a significant expansion in pathogenic Th1 and Vγ4(+) γδ T cells in the periphery of these animals. Furthermore, an increase in regulatory T cells was observed, yet these cells were incapable of controlling myocarditis in H(1)R(-/-) mice. These data establish a critical role for histamine and H(1)R signaling in regulating T cell responses and susceptibility to CVB3-induced myocarditis in B6 mice.

Publication types

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

MeSH terms

  • Animals
  • Coxsackievirus Infections / immunology*
  • Coxsackievirus Infections / metabolism
  • Disease Susceptibility
  • Enterovirus B, Human / immunology*
  • Histamine / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Myocarditis / immunology*
  • Myocarditis / metabolism
  • Receptors, Histamine H1 / deficiency
  • Receptors, Histamine H1 / immunology*
  • Receptors, Histamine H1 / metabolism
  • Signal Transduction
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / metabolism
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / metabolism
  • Th1 Cells / immunology
  • Th1 Cells / metabolism
  • Virus Replication / immunology

Substances

  • Receptors, Histamine H1
  • Histamine