Interferon-gamma inhibits in vitro mobilization of eosinophils by interleukin-5

Int Arch Allergy Immunol. 2005 Mar;136(3):295-302. doi: 10.1159/000083957. Epub 2005 Feb 16.

Abstract

Background: Th2 cytokines play pivotal roles in allergic inflammation, including eosinophilia, and their actions are antagonized by Th1 cytokines, conferring them therapeutic potential.

Methods: In this study, we examined the ability of a number of cytokines to suppress the activation of eosinophils that function as effector cells for allergic airway diseases.

Results: Interleukin (IL)-5, IL-6, and tumor necrosis factor (TNF) induced an eosinophil shape change, whereas interferon (IFN)-gamma significantly inhibited the shape change. Other cytokines, including IL-1beta, IL-4, IL-10 and IL-13, had little or only slightly enhancing or reducing effects on the shape change. We further analyzed the IFN-gamma effect, showing that pretreatment with IFN-gamma strongly suppressed IL-5-induced eosinophil shape change, and cycloheximide (CHX) abrogated the suppression by IFN-gamma, suggesting that new protein synthesis is required for the inhibitory effect by this cytokine. In agreement with these results, IFN-gamma blocked the eosinophil migration and ERK phophorylation induced by IL-5, and the addition of CHX restored eosinophil chemotaxis.

Conclusions: Collectively, IFN-gamma may attenuate eosinophilic inflammation by directly negating eosinophil mobilization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Shape / drug effects*
  • Chemotaxis, Leukocyte / drug effects*
  • Chemotaxis, Leukocyte / immunology
  • Cytokines / immunology
  • Cytokines / pharmacology*
  • Eosinophils / drug effects*
  • Eosinophils / immunology
  • Eosinophils / pathology
  • Extracellular Signal-Regulated MAP Kinases / metabolism*
  • Humans
  • In Vitro Techniques
  • Inflammation / immunology
  • Phosphorylation / drug effects
  • Th1 Cells / immunology
  • Th2 Cells / immunology

Substances

  • Cytokines
  • Extracellular Signal-Regulated MAP Kinases