[Allergic contact dermatitis: how to re-induce tolerance?]

Med Sci (Paris). 2006 Feb;22(2):158-63. doi: 10.1051/medsci/2006222158.
[Article in French]

Abstract

Allergic contact dermatitis (ACD) is a skin inflammatory disease mediated by activation of CD8+ cytotoxic T cells specific for haptens in contact with the skin. CD4+ T cells behave as both regulatory and tolerogenic cells since they down-regulate the skin inflammation in patients with ACD (regulation) and prevent the development of eczema (tolerance) in normal individuals. Thus, ACD corresponds to a breakdown of immune tolerance to haptens in contact with the skin. Several regulatory CD4+ T cell subsets (Treg), especially CD4+CD25+ natural Treg cells, are involved in immunological tolerance and regulation to haptens through the production of the immunosuppressive cytokines IL-10 and TGF-beta. Ongoing strategies to re-induce immune tolerance to haptens in patients with eczema include improvement of existing methods of tolerance induction (oral tolerance, low dose tolerance, allergen-specific immunotherapy, UV-induced tolerance) as well as development of new drugs able to activate IL-10 producing Treg cells in vivo. Ongoing and future progress in this area will open up new avenues for treatment of eczema and more generally autoimmune and allergic diseases resulting from a breakdown of tolerance to autoantigens and allergens, respectively.

Publication types

  • Review

MeSH terms

  • Allergens / adverse effects
  • Allergens / therapeutic use
  • Animals
  • Cytokines / physiology
  • Dermatitis, Allergic Contact / immunology
  • Dermatitis, Allergic Contact / physiopathology
  • Dermatitis, Allergic Contact / therapy*
  • Desensitization, Immunologic
  • Haptens / immunology
  • Haptens / therapeutic use
  • Humans
  • Immune Tolerance*
  • Immunosuppression Therapy / methods*
  • Interleukin-10 / physiology
  • Interleukin-2 / therapeutic use
  • Models, Animal
  • Models, Biological
  • PUVA Therapy
  • T-Lymphocyte Subsets / immunology
  • Transforming Growth Factor beta / physiology

Substances

  • Allergens
  • Cytokines
  • Haptens
  • Interleukin-2
  • Transforming Growth Factor beta
  • Interleukin-10