Phenotypic analysis of CD23+ peripheral blood mononuclear cells in atopic dermatitis

Br J Dermatol. 1991 Dec;125(6):543-7. doi: 10.1111/j.1365-2133.1991.tb14791.x.

Abstract

There is an increase in the number of CD23+ cells in peripheral blood mononuclear cells (PBMC) in atopic dermatitis (AD). We analysed the subpopulation of CD23+ PBMC in 11 patients with AD and in 10 healthy controls and found that B cells (CD20+) and non-T, non-B cells (CD3- CD20-) (mainly monocytes) were responsible for the elevation of CD23+ cells. CD23+ T cells (CD3+) comprised only 4.6% of total CD23+ cells in AD. The percentage of CD23+ cells did not correlate with the serum log IgE level nor with clinical severity of AD. Interleukin 4 (IL-4) induced the expression of CD23 antigen in PBMC both in AD and in healthy controls in a dose-dependent manner in vitro. This enhancing effect of IL-4 was completely abrogated by the addition of anti-IL-4 monoclonal antibody. Other cytokines such as IL-1, IL-2, IL-3, IFN-alpha, IFN-gamma and TNF-alpha had no significant effects on CD23 expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Antigens, CD / drug effects
  • Antigens, CD / immunology*
  • Antigens, Differentiation, B-Lymphocyte / biosynthesis
  • Antigens, Differentiation, B-Lymphocyte / drug effects
  • Antigens, Differentiation, B-Lymphocyte / immunology*
  • Cells, Cultured
  • Child
  • Cytokines / pharmacology
  • Dermatitis, Atopic / immunology*
  • Female
  • Humans
  • Immunoglobulin E / blood
  • Interleukin-4 / pharmacology
  • Leukocytes, Mononuclear / immunology*
  • Male
  • Middle Aged
  • Phenotype
  • Receptors, Fc / biosynthesis
  • Receptors, Fc / drug effects
  • Receptors, Fc / immunology*
  • Receptors, IgE

Substances

  • Antigens, CD
  • Antigens, Differentiation, B-Lymphocyte
  • Cytokines
  • Receptors, Fc
  • Receptors, IgE
  • Interleukin-4
  • Immunoglobulin E