FOXP3+ and CD25+ cells are reduced in patients with stage IV, grade C periodontitis: A comparative clinical study

J Periodontal Res. 2020 Jun;55(3):374-380. doi: 10.1111/jre.12721. Epub 2019 Dec 26.

Abstract

Background and objective: Some studies suggest that regulatory T cells (Tregs) have suppressive effects on inflammatory osteolysis. The aim of this study was to evaluate Treg immunomarkers in periodontitis-affected tissues from patients with periodontitis and clinically healthy gingiva (control).

Material and methods: The presence and distribution of positive cells for CD4, CD25 and FOXP3 (Treg immunomarkers) in periodontitis-affected tissues (epithelium and lamina propria) of 30 patients (ten per group) with a diagnosis of stage IV, grade C periodontitis (IV-C), stage III, grade B periodontitis (III-B) and the control were evaluated. A two-way ANOVA followed by Fisher's LSD test was used to demonstrate differences between the groups and immunomarkers; Student's t test was used to demonstrate differences between the epithelium and the lamina propria.

Results: Both IV-C and III-B periodontitis presented a significantly high proportion of immune-stained cells for all immunomarkers when compared to the control group. Notably, CD25+ and FOXP3+ cells were detected in a significantly higher number in III-B than IV-C periodontitis (P < .05).

Conclusion: Our results suggest the participation of Tregs on the osteoimmunological mechanisms in IV-C and III-B periodontitis patients, notably contributing to strategies for alveolar bone regeneration in clinical treatment decisions.

Keywords: Tregs; immunohistochemistry; immunology; periodontitis.

MeSH terms

  • Biomarkers
  • Case-Control Studies
  • Forkhead Transcription Factors
  • Gingiva
  • Humans
  • Interleukin-2 Receptor alpha Subunit
  • Periodontitis / classification
  • Periodontitis / immunology*
  • T-Lymphocytes, Regulatory / cytology*

Substances

  • Biomarkers
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • IL2RA protein, human
  • Interleukin-2 Receptor alpha Subunit