The chemokine receptor CXCR2 and coronavirus-induced neurologic disease

Virology. 2013 Jan 5;435(1):110-7. doi: 10.1016/j.virol.2012.08.049.

Abstract

Inoculation with the neurotropic JHM strain of mouse hepatitis virus (MHV) into the central nervous system (CNS) of susceptible strains of mice results in an acute encephalomyelitis in which virus preferentially replicates within glial cells while excluding neurons. Control of viral replication during acute disease is mediated by infiltrating virus-specific T cells via cytokine secretion and cytolytic activity, however sterile immunity is not achieved and virus persists resulting in chronic neuroinflammation associated with demyelination. CXCR2 is a chemokine receptor that upon binding to specific ligands promotes host defense through recruitment of myeloid cells to the CNS as well as protecting oligodendroglia from cytokine-mediated death in response to MHV infection. These findings highlight growing evidence of the diverse and important role of CXCR2 in regulating neuroinflammatory diseases.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Acute Disease
  • Animals
  • Cell Movement
  • Central Nervous System / immunology
  • Central Nervous System / pathology
  • Central Nervous System / virology*
  • Coronavirus Infections / immunology
  • Coronavirus Infections / pathology
  • Coronavirus Infections / virology*
  • Cytokines / biosynthesis
  • Demyelinating Diseases / immunology
  • Demyelinating Diseases / pathology
  • Demyelinating Diseases / virology*
  • Encephalomyelitis / immunology
  • Encephalomyelitis / pathology
  • Encephalomyelitis / virology*
  • Mice
  • Murine hepatitis virus / pathogenicity
  • Murine hepatitis virus / physiology*
  • Myeloid Cells / immunology
  • Myeloid Cells / virology
  • Oligodendroglia / immunology
  • Oligodendroglia / pathology
  • Oligodendroglia / virology*
  • Receptors, Interleukin-8B / genetics
  • Receptors, Interleukin-8B / immunology*
  • T-Lymphocytes / immunology
  • T-Lymphocytes / virology
  • Virus Replication

Substances

  • Cytokines
  • Receptors, Interleukin-8B