Mold elicits atopic dermatitis by reactive oxygen species: Epidemiology and mechanism studies

Clin Immunol. 2015 Dec;161(2):384-90. doi: 10.1016/j.clim.2015.07.007. Epub 2015 Jul 21.

Abstract

Mold has been implicated in the development of atopic dermatitis (AD); however, the underlying mechanisms remain unknown. The aim of the study was to investigate the effects of mold exposure in early life through epidemiologic and mechanistic studies in vivo and in vitro. Exposure to visible mold inside the home during the first year of life was associated with an increased risk for current AD by two population-based cross-sectional human studies. Children with the AG+GG genotype of GSTP1 showed increased risk for current AD when exposed to mold. In the mouse model, treatment with patulin induced and aggravated clinically significant AD and Th2-related inflammation of the affected mouse skin. Additionally, reactive oxygen species (ROS) were released in the mouse skin as well by human keratinocytes. In conclusions, mold exposure increases the risk for AD related to ROS generation mediated by Th2-promoting inflammatory cytokines.

Keywords: Atopic dermatitis; Mold; Reactive oxygen species; Thymic stromal lymphopoietin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Animals
  • Child
  • Child, Preschool
  • Cohort Studies
  • Cross-Sectional Studies
  • Cytokines / immunology
  • Cytokines / metabolism
  • Dermatitis, Atopic / genetics
  • Dermatitis, Atopic / immunology*
  • Dermatitis, Atopic / metabolism
  • Disease Models, Animal
  • Female
  • Fungi / immunology*
  • Genetic Predisposition to Disease / epidemiology
  • Genetic Predisposition to Disease / genetics
  • Genotype
  • Glutathione S-Transferase pi / genetics
  • Glutathione S-Transferase pi / immunology
  • Humans
  • Infant
  • Infant, Newborn
  • Keratinocytes / immunology
  • Keratinocytes / metabolism
  • Male
  • Mice, Hairless
  • Reactive Oxygen Species / immunology*
  • Reactive Oxygen Species / metabolism
  • Republic of Korea / epidemiology
  • Risk Factors
  • Skin / immunology*
  • Skin / metabolism
  • Skin / pathology
  • Th2 Cells / immunology
  • Th2 Cells / metabolism

Substances

  • Cytokines
  • Reactive Oxygen Species
  • GSTP1 protein, human
  • Glutathione S-Transferase pi