IFN-gamma but not IL-4 T cells of the asthmatic bronchial wall show increased incidence of apoptosis

Clin Exp Allergy. 2001 May;31(5):731-9. doi: 10.1046/j.1365-2222.2001.01099.x.


Background: Previous observations have established that IFN-gamma production is depressed in CD4+ T cells from atopic asthmatics compared with non-asthmatics.

Objective: The aim of this study was to determine if decreased IFN-gamma production could be due to a dissociation between levels of apoptosis within the T cell subsets of the asthmatic bronchial wall.

Methods: Twenty asthmatics (10 atopic and 10 non-atopic) and eight non-atopic non-asthmatics underwent bronchoscopy. Cryostat sections of these biopsies were investigated using immunohistological techniques to determine the relative number of CD4/FAS+ and CD4/Bcl-2+ cells. Detection of IFN-gamma+ and IL-4+ was combined with TUNEL staining to determine the proportions of the Th1 and Th2 cells undergoing apoptosis.

Results: Experiments revealed raised proportions of activated CD4+ T cells as assessed by expression of HLA-DR and CD25+ expression in the asthmatic samples. Expression of Bcl-2 by the CD4+ cell population was significantly reduced in the asthmatic compared with the control group (P = 0.002). There was no significant difference in the expression of CD4+ Fas-ligand or the number of CD4+ undergoing apoptosis in the asthmatic and non-asthmatic groups. However, the IFN-gamma+ (P = 0.04) but not IL-4+ T cells in the asthmatic biopsies had significantly higher proportions of apoptotic cells compared with the control group.

Conclusion: The evidence supports the hypothesis that Th1/Th2 imbalance in asthmatic inflammation may be a result of premature apoptosis within the Th1 subset.

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Apoptosis / physiology*
  • Asthma / metabolism*
  • Asthma / pathology*
  • Biopsy
  • Bronchi / pathology*
  • CD4-Positive T-Lymphocytes / physiology
  • CD8-Positive T-Lymphocytes / physiology
  • Gene Expression / physiology
  • Genes, bcl-2 / genetics
  • HLA-DR Antigens / biosynthesis
  • Humans
  • In Situ Nick-End Labeling / methods
  • Incidence
  • Interferon-gamma / metabolism*
  • Interleukin-4 / metabolism*
  • Middle Aged
  • T-Lymphocyte Subsets / metabolism
  • T-Lymphocytes / metabolism*


  • HLA-DR Antigens
  • Interleukin-4
  • Interferon-gamma