Dendritic cell number is related to IL-4 expression in the airways of atopic asthmatic subjects

Allergy. 2000 May;55(5):449-54. doi: 10.1034/j.1398-9995.2000.055005449.x.

Abstract

Background: Airway dendritic cells are essential for stimulating naive T cells in response to inhaled antigen and for the development of allergic sensitization. IL-4 in vitro can distinguish dendritic cell lines from peripheral blood mononuclear cells. Our study had the following aims: 1) to compare the distribution of CD1a+ dendritic cells and IL-4+ cells, in the bronchial mucosa of asthmatics and controls 2) to determine the relationship between the numbers of CD1a+ dendritic cells and IL-4+ cells in the bronchial mucosa of asthmatics 3) to determine whether CD1a+ cells express the IL-4 receptor.

Methods: Twenty atopic asthmatic and eight normal subjects were studied. In each subject, bronchoscopy with bronchial biopsies was performed. CD1a, IL-4, and IL-4 receptor expressions were evaluated by immunohistochemistry.

Results: The number of CD1a+ and IL-4+ cells was significantly higher in asthmatics than controls. The number of CD1a+ cells was positively correlated to the number of IL-4 + cells. Bronchial biopsy serial section studies showed that CD1a+ cells express the receptor for IL-4.

Conclusions: These results suggest that an increased amount of IL-4 may play a physiopathologic role in maintaining the dendritic cell pool in vivo. Therefore, because of possible IL-4 activity on antigen-presenting cells in T-cell immune responses to allergens, an important new role of IL-4 in asthma inflammation can be envisaged.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Antigens, CD1 / analysis
  • Asthma / immunology*
  • Asthma / pathology
  • Biopsy
  • Bronchi / pathology
  • Cell Count
  • Dendritic Cells / immunology*
  • Female
  • Humans
  • Immunohistochemistry
  • Interleukin-4 / analysis*
  • Male
  • Middle Aged
  • Receptors, Interleukin-4 / analysis
  • Respiratory Mucosa / pathology

Substances

  • Antigens, CD1
  • Receptors, Interleukin-4
  • Interleukin-4