Transcription Factor AhR, Cytokines IL-6 and IL-22 in Subjects with and without Peri-Implantitis: A Case Control-Study

Int J Environ Res Public Health. 2022 Jun 17;19(12):7434. doi: 10.3390/ijerph19127434.

Abstract

Peri-implantitis is a plaque-associated condition characterized by mucosal inflammation and subsequent progressive loss of supporting bone; it is caused by bacterial biofilm, but the host response triggered by bacterial stimulation promotes the release of cells and mediators that culminate in tissue destruction. The Aryl-hydrocarbon Receptor (AhR) is associated with IL-22 production by Th22 and Th17 CD4+ Th cells. The presence of IL-6 may promote the Th22 phenotype. The present case-control study evaluated the gene expression of AhR, IL-22, and IL-6 in the peri-implant tissues of healthy and peri-implantitis patients. Tissue biopsies were collected from thirty-five volunteers (15 healthy and 20 with peri-implantitis). A real-time PCR reaction was utilized to assess the AhR, IL-22, and IL-6 gene expression levels relative to the reference gene (GAPDH). The results were analyzed using the Mann-Whitney test with a significance level of 5%. Higher levels of gene expression of AhR and IL-6 were detected in peri-implantitis tissues. The IL-22 gene expression levels did not differ between groups. In conclusion, higher gene expression levels for AhR and IL-6 were detected in the soft tissues of peri-implantitis patients. IL-22 did not vary between conditions, which may indicate the loss of the immunomodulatory role of IL-22 in periimplantitis.

Keywords: Th22 lymphocytes; gene expression; interleukin-22; interleukin-6; peri-implantitis; transcription factor aryl-hydrocarbon receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Case-Control Studies
  • Cytokines / metabolism
  • Humans
  • Interleukin-22
  • Interleukin-6 / genetics
  • Interleukins
  • Peri-Implantitis* / genetics
  • Receptors, Aryl Hydrocarbon / metabolism

Substances

  • AHR protein, human
  • Basic Helix-Loop-Helix Transcription Factors
  • Cytokines
  • Interleukin-6
  • Interleukins
  • Receptors, Aryl Hydrocarbon

Grants and funding

J.A.S. was funded by CNPq # 301527/2006-7, # 504392/2010-7 and 311368/2019-0; FAPESP # 2008/07154-5.