Th1 cytokines in oral lichen planus

J Oral Pathol Med. 2003 Feb;32(2):77-83. doi: 10.1034/j.1600-0714.2003.00077.x.

Abstract

Background: Cell-mediated immune responses in oral lichen planus (OLP) may be regulated by cytokines and their receptors.

Methods: In situ cytokine expression and in vitro cytokine secretion in OLP were determined by immunohistochemistry and ELISA.

Results: The majority of subepithelial and intraepithelial mononuclear cells in OLP were CD8+. In some cases, intraepithelial CD8+ cells were adjacent to degenerating keratinocytes. CD4+ cells were observed mainly in the deep lamina propria with occasional CD4+ cells close to basal keratinocytes. Mononuclear cells expressed IFN-gamma in the superficial lamina propria and TNF-alpha adjacent to basal keratinocytes. Basal keratinocytes expressed TNF-alpha as a continuous band. TNF R1 was expressed by mononuclear cells and basal and suprabasal keratinocytes. There was variable expression of TGF-beta1 in the subepithelial infiltrate while all intraepithelial mononuclear cells were TGF-beta1-. Keratinocytes in OLP stained weakly for TGF-beta1. Unstimulated OLP lesional T cells secreted IFN-gamma in vitro. TNF-alpha stimulation down-regulated IFN-gamma secretion and up-regulated TNF-alpha secretion. IL-4, IL-10 and TGF-beta1 secretion were not detected.

Conclusions: These data suggest the development of a T helper 1 immune response that may promote CD8+ cytotoxic T-cell activity in OLP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Aged
  • CD8-Positive T-Lymphocytes
  • Cell Count
  • Cells, Cultured
  • Cytokines / biosynthesis
  • Cytokines / immunology*
  • Humans
  • Immunohistochemistry
  • Interferon-gamma / biosynthesis
  • Interferon-gamma / immunology
  • Keratinocytes / pathology
  • Lichen Planus, Oral / immunology*
  • Male
  • Middle Aged
  • Receptors, Immunologic / immunology
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / metabolism
  • T-Lymphocytes, Cytotoxic / physiology
  • Th1 Cells / immunology*
  • Th1 Cells / metabolism
  • Transforming Growth Factor beta / biosynthesis
  • Transforming Growth Factor beta / immunology
  • Transforming Growth Factor beta1
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • Cytokines
  • Receptors, Immunologic
  • TGFB1 protein, human
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta1
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma