IL-23 and T(H)17-mediated inflammation in human allergic contact dermatitis

J Allergy Clin Immunol. 2009 Feb;123(2):486-92. doi: 10.1016/j.jaci.2008.09.036. Epub 2008 Nov 4.

Abstract

Background: IL-17-producing T(H) (T(H)17) cells are key mediators of chronic inflammation in mice. Recent studies have implicated T(H)17-mediated inflammation in the pathogenesis of human autoimmune diseases; however, the involvement of T(H)17 cells in allergic disorders remains largely elusive.

Objective: To investigate T(H)17-mediated inflammation in human beings with allergic contact dermatitis; in particular, the innate response of keratinocytes to contact allergen, the induction of allergen-specific T(H)17 cells, and the presence of T(H)17-related effector cells in inflamed skin.

Methods: Human keratinocytes were stimulated with nickel in vitro followed by measurements of IL-23 and IL-12 production by quantitative PCR and ELISA. Allergen-specific memory T cells from the blood of individuals with nickel allergy and healthy controls were identified and characterized by using a short-term ex vivo assay. Nickel patch test lesions and normal skin were analyzed for the expression of T(H)17-related cells and molecules by using immunohistochemistry.

Results: Keratinocytes were found to produce IL-23, but no detectable IL-12, in a response to nickel stimulation. Memory T cells isolated from peripheral blood of individuals with nickel allergy, but not healthy controls, contained T(H)17 and T(H)1 cells proliferating in response to nickel-pulsed DCs. Inflamed skin of nickel-challenged allergic individuals contained infiltrating neutrophils and cells expressing IL-17, IL-22, CCR6, and IL-22R.

Conclusion: Our results demonstrate the involvement of T(H)17-mediated immunopathology in human allergic contact dermatitis, including both innate and adaptive immune responses to contact allergens.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allergens / immunology
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Dermatitis, Allergic Contact / immunology*
  • Dermatitis, Allergic Contact / metabolism
  • Humans
  • Inflammation / immunology*
  • Inflammation / metabolism
  • Interleukin-12 / immunology
  • Interleukin-12 / metabolism
  • Interleukin-17 / immunology*
  • Interleukin-17 / metabolism
  • Interleukin-22
  • Interleukin-23 / biosynthesis
  • Interleukin-23 / immunology*
  • Interleukin-23 / pharmacology
  • Interleukins / immunology
  • Interleukins / metabolism
  • Keratinocytes / immunology*
  • Keratinocytes / metabolism
  • Nickel / immunology
  • Receptors, CCR6 / immunology
  • Receptors, CCR6 / metabolism
  • Receptors, Interleukin / immunology
  • Receptors, Interleukin / metabolism
  • T-Lymphocytes, Helper-Inducer / drug effects
  • T-Lymphocytes, Helper-Inducer / immunology*
  • T-Lymphocytes, Helper-Inducer / metabolism

Substances

  • Allergens
  • CCR6 protein, human
  • Interleukin-17
  • Interleukin-23
  • Interleukins
  • Receptors, CCR6
  • Receptors, Interleukin
  • interleukin-22 receptor
  • Interleukin-12
  • Nickel