IL-18 skews the invariant NKT-cell population via autoreactive activation in atopic eczema

Eur J Immunol. 2009 Aug;39(8):2293-301. doi: 10.1002/eji.200839195.

Abstract

Atopic eczema (AE) is a chronic relapsing inflammatory skin disease where the commensal yeast Malassezia can act as a microbial trigger factor. Malassezia activates human DC to produce IL-18, an innate cytokine that is elevated in serum of AE patients; however, the precise role of IL-18 in human AE etiology is unknown. Herein, we investigated the effect of IL-18 on the human invariant NKT (iNKT) cell compartment in AE. We found that IL-18 was a potent activator of human iNKT-cells and promoted a pro-inflammatory CD1d-dependent response, even in the absence of exogenous ligands. Chronic activation via IL-18 on the other hand was inhibitory and skewed the iNKT-cell pool by selectively suppressing CD4(+) iNKT-cells. This was mimicked in AE patients where the proportion of CD4(+) iNKT-cells was reduced in peripheral blood and coincided with elevated plasma levels of IL-18. Furthermore, a reduced CD4(+) iNKT-cell pool was associated with elevated IgE levels in plasma, and the plasma levels of IL-18 correlated with both total IgE and disease severity in the AE patients. Based on these findings, we propose that IL-18-mediated activation and subsequent dysregulation of the CD1d-restricted iNKT-cells plays a role in the pathogenesis of human AE.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Animals
  • Antibodies, Fungal / blood
  • Antigens, CD1d / genetics
  • Antigens, CD1d / metabolism
  • Cell Line
  • Cells, Cultured
  • Dermatitis, Atopic / blood
  • Dermatitis, Atopic / metabolism*
  • Dermatitis, Atopic / pathology
  • Female
  • Humans
  • Immunoglobulin E / blood
  • Interferon gamma Receptor
  • Interferon-gamma / metabolism
  • Interleukin-18 / blood
  • Interleukin-18 / metabolism*
  • Interleukin-18 / pharmacology
  • Malassezia / immunology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Middle Aged
  • NF-kappa B / metabolism*
  • Natural Killer T-Cells / cytology
  • Natural Killer T-Cells / drug effects
  • Natural Killer T-Cells / metabolism*
  • Receptors, Interferon / genetics
  • Receptors, Interferon / metabolism
  • Signal Transduction
  • Young Adult

Substances

  • Antibodies, Fungal
  • Antigens, CD1d
  • Interleukin-18
  • NF-kappa B
  • Receptors, Interferon
  • Immunoglobulin E
  • Interferon-gamma