T lymphocytes and altered keratinocytes express interferon-gamma and interleukin 6 in lichen planus

Arch Dermatol Res. 1999 Sep;291(9):485-90. doi: 10.1007/s004030050442.

Abstract

Lichen planus is assumed to represent a delayed hypersensitivity reaction, in the course of which cytokines control the proliferation and differentiation of cytotoxic T lymphocytes which attack the epidermis and cause apoptosis of undifferentiated keratinocytes. Since interferon-gamma and interleukin 6 are known to be markedly generated in lichen planus, we investigated the cellular localization of these cytokines in affected skin/oral mucosa biopsy specimens using in situ hybridization for interferon-gamma and in situ reverse transcription-polymerase chain reaction for interleukin 6 mRNA. In the upper subepithelial connective tissue interferon-gamma mRNA was noted within proliferating CD3+ T lymphocytes. In this tissue compartment interleukin 6 mRNA was detected in infiltrating CD4+ and CD8+ T lymphocytes. In the epithelium, expression of interferon-gamma mRNA and interleukin 6 mRNA was observed in the basal and suprabasal keratinocytes of altered skin/oral mucosa. In contrast, normal skin did not reveal any interferon-gamma or interleukin 6 expression, although a few CD4+ and CD8+ T lymphocytes were noted in the dermis as well as the epidermis. These findings indicate that in lichen planus the proinflammatory cytokines interferon-gamma and interleukin 6 are produced not only by activated T lymphocytes but also by altered keratinocytes, and suggest that stimulated keratinocytes may amplify the course of lichen planus.

MeSH terms

  • Biopsy
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • Interferon-gamma / genetics
  • Interferon-gamma / metabolism*
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism*
  • Keratinocytes / metabolism*
  • Lichen Planus / metabolism*
  • Lichen Planus / pathology
  • RNA, Messenger / metabolism
  • Reference Values
  • Reverse Transcriptase Polymerase Chain Reaction
  • Skin / metabolism
  • Skin / pathology
  • T-Lymphocytes / metabolism*

Substances

  • Interleukin-6
  • RNA, Messenger
  • Interferon-gamma