IL-1 beta protein in human skin lymph does not discriminate allergic from irritant contact dermatitis

Contact Dermatitis. 1996 Sep;35(3):152-6. doi: 10.1111/j.1600-0536.1996.tb02333.x.

Abstract

Recent data suggest a key rôle for IL-1 beta in the induction phase of allergic contact dermatitis. In the present study, the protein levels of IL-1 beta were measured in skin lymph derived from normal untreated skin as well as from irritant and allergic (induction and elicitation phase) contact dermatitis. IL-1 beta increased in the course of both types of contact dermatitis, displaying the highest levels in irritant CD. Using a reverse transcriptase-polymerase chain reaction, low signal strength of IL-1 beta mRNA was demonstrated in lymph cells derived from normal skin and allergic CD. In lymph cells collected 2 x daily during the induction phase of allergic contact dermatitis, no upregulation of the IL-1 beta mRNA signal was found. Isolated CD1a+ lymph cells derived from normal skin as well as from the induction and elicitation phase of allergic contact dermatitis did not express IL-1 beta mRNA. Our results demonstrate that in human skin lymph, the IL-1 beta profiles do not discriminate between irritant and allergic contact dermatitis and that besides resident epidermal and dermal cells, circulating lymph cells may also contribute to IL-1 beta protein production.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Allergens
  • Cyclopropanes
  • Dermatitis, Allergic Contact / immunology*
  • Dermatitis, Irritant / immunology*
  • Dinitrochlorobenzene
  • Epidermis / immunology
  • Epidermis / pathology
  • Female
  • Humans
  • Interleukin-1 / analysis*
  • Interleukin-1 / genetics
  • Irritants
  • Langerhans Cells / immunology
  • Lymph / immunology*
  • Lymphocytes / immunology
  • Male
  • Polymerase Chain Reaction
  • RNA, Messenger / analysis
  • RNA, Messenger / genetics
  • RNA-Directed DNA Polymerase
  • Skin / immunology*
  • Skin / pathology
  • Sodium Dodecyl Sulfate
  • Transcription, Genetic
  • Up-Regulation

Substances

  • Allergens
  • Cyclopropanes
  • Dinitrochlorobenzene
  • Interleukin-1
  • Irritants
  • RNA, Messenger
  • Sodium Dodecyl Sulfate
  • RNA-Directed DNA Polymerase
  • diphenylcyclopropenone