Proinflammatory and regulatory mechanisms in allergic contact dermatitis caused by methylchloroisothiazolinone and methylisothiazolinone

Exp Dermatol. 2020 May;29(5):490-498. doi: 10.1111/exd.14086. Epub 2020 Apr 15.

Abstract

Background: Methylchloroisothiazolinone (MCI) and methylisothiazolinone (MI) are the cause of an increasing number of contact allergies. Understanding the mechanisms by which MCI/MI induces proinflammatory and regulatory factors production is necessary to understand the outcome of allergic contact dermatitis (ACD).

Objectives: To evaluate the dysfunction of proinflammatory cytokines and regulatory factors in the positive MCI/MI patch test at the transcriptional and protein expression levels. Moreover, to analyse the cytokines production induced by MI in peripheral blood mononuclear cells (PBMCs).

Materials and methods: The selected patients had positive MCI/MI patch test results. The expression of proinflammatory factors was evaluated by q-PCR and immunochemistry at 48 hours of positive MCI/MI patch test. The MCI/MI- or MI- induced secretion of IL-1β, TNF and IL-6 by PBMC was analysed by flow cytometry.

Results: The results showed a decreased TLR4 expression with upregulated IL6, FOXP3, IL10 and TGFβ mRNA expression as assessed by q-PCR at the site of the MCI/MI skin reaction. We detected increased protein levels of TLR4, FOXP3 and IL-10 in the dermis layer in the ACD reaction by immunocitochemistry. Moreover, MCI/MI induced proinflammatory cytokine production by PBMC through the NF-κB signalling pathway.

Conclusion: Considering the altered innate immune response triggered by MCI/MI sensitization, these findings indicate that the regulatory process at the induction phase of ACD is a crucial mechanism. Given the increase in occupational and domestic exposure to MCI/MI, the underlying immunological mechanisms should be understood.

Keywords: IL-10; TLR4; allergic contact dermatitis; cytokines; methylchloroisothiazolinone; methylisothiazolinone; regulatory T cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Cytokines / metabolism
  • Dermatitis, Allergic Contact / immunology*
  • Dermatitis, Allergic Contact / physiopathology*
  • Female
  • Forkhead Transcription Factors / biosynthesis
  • Humans
  • Inflammation
  • Interleukin-10 / biosynthesis
  • Interleukin-1beta / metabolism
  • Interleukin-6 / biosynthesis
  • Interleukin-6 / metabolism
  • Leukocytes, Mononuclear / cytology
  • Male
  • Mice
  • Middle Aged
  • Signal Transduction
  • Thiazoles / adverse effects*
  • Toll-Like Receptor 4 / biosynthesis
  • Transforming Growth Factor beta1 / biosynthesis
  • Tumor Necrosis Factor-alpha / metabolism
  • Young Adult

Substances

  • Cytokines
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • IL10 protein, human
  • IL6 protein, human
  • Interleukin-1beta
  • Interleukin-6
  • TGFB1 protein, human
  • TLR4 protein, human
  • Thiazoles
  • Toll-Like Receptor 4
  • Transforming Growth Factor beta1
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • 2-methyl-4-isothiazolin-3-one
  • 5-chloro-2-methyl-4-isothiazolin-3-one