Staphylococcal α-toxin induces a higher T cell proliferation and interleukin-31 in atopic dermatitis

Int Arch Allergy Immunol. 2011;156(4):412-5. doi: 10.1159/000323905. Epub 2011 Aug 10.

Abstract

Background: Patients with atopic dermatitis (AD) are frequently colonized with α-toxin-producing Staphylococcus aureus which is in turn positively correlated with the severity of eczema.

Methods: IN this study we addressed T cell proliferation and T cell as well as monocyte cytokine secretion upon α-toxin stimulation in peripheral blood mononuclear cells (PBMCs) from AD patients compared to healthy controls.

Results: We found that α-toxin stimulation of PBMCs markedly enhanced T cell proliferation both in patients with AD and healthy controls and was significantly increased in AD patients compared to healthy controls. PBMCs of AD patients secreted significantly more IL-31 compared to those of healthy controls upon α-toxin and SEB stimulation. Moreover, α-toxin stimulation yielded an increase in T cell (IL-2, IL-9, IL-10 and IFN-γ) as well as monocyte (IL-1β and TNF-α) cytokine secretion.

Conclusion: Our results could partly explain how skin colonization and infection with S. aureus can contribute to chronic skin inflammation and pruritus in AD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Toxins / pharmacology*
  • Cells, Cultured
  • Cytokines / metabolism
  • Dermatitis, Atopic / immunology*
  • Hemolysin Proteins / pharmacology*
  • Humans
  • Interleukins / metabolism*
  • Leukocytes, Mononuclear / drug effects
  • Leukocytes, Mononuclear / immunology
  • Lymphocyte Activation / drug effects
  • Lymphocyte Activation / immunology*
  • T-Lymphocytes, Helper-Inducer / drug effects
  • T-Lymphocytes, Helper-Inducer / immunology*

Substances

  • Bacterial Toxins
  • Cytokines
  • Hemolysin Proteins
  • IL31 protein, human
  • Interleukins
  • staphylococcal alpha-toxin