Expression of lymphocytes Fc epsilon RII/CD23 in allergic children undergoing hyposensitization

Int Arch Allergy Immunol. 1993;101(2):203-8. doi: 10.1159/000236520.

Abstract

Owing to the proposed role of Fc epsilon RII/CD23 in allergic diseases, we analyzed the expression of this receptor on peripheral blood lymphocytes (pan-B, pan-T and CD4+ or CD8+ T cells) and its autoproteolytic product sCD23 in serum. This was done in 10 asthmatic children allergic to Dermatophagoides pteronyssinus (Dpt) before and 6 weeks after hyposensitization. FACS analysis of double, direct immunofluorescence staining of the whole blood revealed an elevated percentage of Fc epsilon RII/CD23+ lymphocytes in allergic children (10.29 +/- 5.0), a significantly higher percentage than in nonallergic children (5.7 +/- 2.4, p < 0.05). The majority of Fc epsilon RII/CD23+ were on B cells. A significant positive correlation between the percentages of CD23+ lymphocytes and serum IgE levels was found (Spearman rank = 0.63, p < 0.05). The percentage of CD20+CD23+ lymphocytes significantly decreased after 6 weeks of hyposensitization (6.2 +/- 3.6, p < 0.05), while the percentage of CD20+ lymphocytes remained unchanged. Similarly, hyposensitization was followed by a reduction of total serum IgE levels, but Dpt-specific IgG4 and IgE remained unchanged.

MeSH terms

  • Allergens / immunology
  • Animals
  • Antigens, CD / blood
  • Antigens, CD20
  • Antigens, Dermatophagoides
  • Antigens, Differentiation, B-Lymphocyte / blood
  • Asthma / immunology*
  • Asthma / therapy
  • Child
  • Child, Preschool
  • Desensitization, Immunologic*
  • Female
  • Flow Cytometry
  • Humans
  • Hypersensitivity / immunology*
  • Hypersensitivity / therapy
  • Immunoglobulin E / blood
  • Immunoglobulin G / blood
  • Immunophenotyping
  • Lymphocyte Subsets / immunology*
  • Male
  • Mites / immunology
  • Receptors, IgE / analysis*
  • Receptors, IgE / immunology*

Substances

  • Allergens
  • Antigens, CD
  • Antigens, CD20
  • Antigens, Dermatophagoides
  • Antigens, Differentiation, B-Lymphocyte
  • Immunoglobulin G
  • Receptors, IgE
  • Immunoglobulin E