Measle virus-infected dendritic cells develop immunosuppressive and cytotoxic activities

Immunobiology. 2001 Dec;204(5):629-38. doi: 10.1078/0171-2985-00102.

Abstract

Measle virus (MV) infection induces a transient but profound immunosuppression characterized by a panlymphopenia which occasionally results in opportunistic infections responsible for a high rate of mortality in malnourished children. MV can encounter human dendritic cells (DC) in the respiratory mucosa or in the secondary lymphoid organs. After a brief presentation of DCs, we review progress in understanding the immunobiology of MV-infected DCs that could account for MV-induced immunosuppression. In addition, we develop the newly described TRAIL-mediated cytotoxic function of DCs that is turned on by MV infection, but also by interferons or double-stranded RNA (poly (I:C)). Finally, we propose a model where the measles-associated lymphopenia could be mediated by TRAIL and the measles-induced immunosuppression could be transiently prolonged by Fas-mediated destruction of DCs.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adaptation, Physiological / immunology
  • Animals
  • Apoptosis Regulatory Proteins
  • Cytotoxicity, Immunologic / immunology*
  • Dendritic Cells / immunology*
  • Dendritic Cells / virology
  • Humans
  • Immune Tolerance / immunology*
  • Immunity, Active / immunology
  • Ligands
  • Measles / immunology*
  • Measles virus / immunology
  • Membrane Glycoproteins / immunology*
  • TNF-Related Apoptosis-Inducing Ligand
  • Tumor Necrosis Factor-alpha / immunology*

Substances

  • Apoptosis Regulatory Proteins
  • Ligands
  • Membrane Glycoproteins
  • TNF-Related Apoptosis-Inducing Ligand
  • TNFSF10 protein, human
  • Tumor Necrosis Factor-alpha