Possible mechanisms of neutrophil activation in Behçet's disease

Int Immunopharmacol. 2013 Dec;17(4):1206-10. doi: 10.1016/j.intimp.2013.07.017. Epub 2013 Aug 23.

Abstract

Behçet's disease (BD) is a systemic inflammatory disorder characterized by recurrent episodes of acute inflammation consisting mainly of neutrophil infiltration around blood vessels in affected tissues. BD probably occurs due to neutrophil-based innate immune responses orchestrated by a complex interplay among gamma-delta T lymphocytes, natural killer T cells, monocytes and Th17 lymphocytes in which type-I interferon is possibly a key element for inflammatory downregulation. However, strong evidence is still scarce. This article compiles the literature in an attempt to summarize the possible mechanisms by which neutrophils are activated in BD and suggests directions for future research.

Keywords: Behçet's disease; Inflammation; Neutrophils.

Publication types

  • Review

MeSH terms

  • Animals
  • Behcet Syndrome / immunology*
  • Granulocyte Colony-Stimulating Factor / immunology
  • Granulocyte-Macrophage Colony-Stimulating Factor / immunology
  • Humans
  • Interferon Type I / immunology
  • Interleukin-8 / immunology
  • Neutrophil Activation*
  • Neutrophils / immunology*
  • Th17 Cells / immunology
  • Toll-Like Receptors / immunology

Substances

  • Interferon Type I
  • Interleukin-8
  • Toll-Like Receptors
  • Granulocyte Colony-Stimulating Factor
  • Granulocyte-Macrophage Colony-Stimulating Factor