Echovirus infection causes rapid loss-of-function and cell death in human dendritic cells

Cell Microbiol. 2007 Jun;9(6):1507-18. doi: 10.1111/j.1462-5822.2007.00888.x. Epub 2007 Feb 9.

Abstract

Coxsackie B viruses (CVB) and Echoviruses (EV) form a single species; Human enterovirus B (HeV-B), within the genus Enterovirus. Although HeV-B infections are usually mild or asymptomatic, they can cause serious acute illnesses. In addition, HeV-B infections have been associated with chronic immune disorders, such as type 1 diabetes mellitus and chronic myocarditis/dilated cardiomyopathy. It has therefore been suggested that these viruses may trigger an autoimmune process. Here, we demonstrate that human dendritic cells (DCs), which play an essential role in orchestration of the immune response, are productively infected by EV, but not CVB strains, in vitro. Infection does not result in DC activation or the induction of antiviral immune responses. Instead, EV infection rapidly impedes Toll-like receptor-mediated production of cytokines and upregulation of maturation markers, and ultimately causes loss of DC viability. These results describe for the first time the effect of EV on the function and viability of human DCs and suggest that infection of DCs in vivo can impede regulation of immune responses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Adhesion Molecules / metabolism
  • Cell Death*
  • Coxsackievirus Infections / immunology
  • Dendritic Cells / cytology
  • Dendritic Cells / immunology
  • Dendritic Cells / virology*
  • Echovirus Infections / immunology*
  • Enterovirus B, Human / immunology*
  • Humans
  • Lectins, C-Type / metabolism
  • Monocytes / cytology
  • Monocytes / virology
  • Receptors, Cell Surface / metabolism
  • Toll-Like Receptors / immunology
  • Transfection

Substances

  • Cell Adhesion Molecules
  • DC-specific ICAM-3 grabbing nonintegrin
  • Lectins, C-Type
  • Receptors, Cell Surface
  • Toll-Like Receptors