Herpes virus entry mediator synergizes with Toll-like receptor mediated neutrophil inflammatory responses

Immunology. 2006 Nov;119(3):404-11. doi: 10.1111/j.1365-2567.2006.02449.x.

Abstract

In microbial infections polymorphnuclear neutrophils (PMN) constitute a major part of the innate host defence, based upon their ability to rapidly accumulate in inflamed tissues and clear the site of infection from microbial pathogens by their potent effector mechanisms. The recently described transmembrane receptor herpes virus entry mediator (HVEM) is a member of the tumour necrosis factor receptor super family and is expressed on many haematopoietic cells, including T cells, B cells, natural killer cells, monocytes and PMN. Interaction of HVEM with the natural ligand LIGHT on T cells has a costimulatory effect, and increases the bactericidal activity of PMN. To further characterize the function of HVEM on PMN, we evaluated the effect of receptor ligation on human PMN effector functions using an agonistic monoclonal antibody. Here we demonstrate that activation of HVEM causes activation of neutrophil effector functions, including respiratory burst, degranulation and release of interleukin-8 in synergy with ligands for Toll-like receptors or GM-CSF. In addition, stimulation via HVEM enhanced neutrophil phagocytic activity of complement opsonized, but not of non-opsonized, particles. In conclusion, these results indicate a new, as yet unknown, participation of HVEM in the innate immune response and points to a new link between innate and adaptive immunity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Degranulation / immunology
  • Cell Survival / immunology
  • Cells, Cultured
  • Humans
  • Inflammation Mediators / immunology
  • Interleukin-8 / metabolism
  • Ligands
  • Neutrophil Activation / immunology*
  • Neutrophils / immunology*
  • Phagocytosis / immunology
  • Receptors, Tumor Necrosis Factor, Member 14 / immunology*
  • Respiratory Burst / immunology
  • Toll-Like Receptors / immunology*

Substances

  • Inflammation Mediators
  • Interleukin-8
  • Ligands
  • Receptors, Tumor Necrosis Factor, Member 14
  • TNFRSF14 protein, human
  • Toll-Like Receptors