Increased expression of interleukin-16 in bronchial mucosa of subjects with atopic asthma

S Laberge, P Ernst, O Ghaffar… - American journal of …, 1997 - atsjournals.org
S Laberge, P Ernst, O Ghaffar, WW Cruikshank, H Kornfeld, DM Center, Q Hamid
American journal of respiratory cell and molecular biology, 1997atsjournals.org
Asthma is characterized by the presence of activated CD4+ cells in the airways. We
hypothesized that the newly characterized cytokine interleukin (IL)-16 is involved in the
pathogenesis of asthma through its ability to selectively induce CD4+ cell recruitment within
the inflamed bronchial wall. We investigated the expression of IL-16 in bronchial biopsies
obtained from subjects with mild asthma (n= 10), atopic nonasthmatic individuals (n= 6), and
normal control subjects (n= 10). Cryostat sections from 4% paraformaldehyde-fixed …
Asthma is characterized by the presence of activated CD4+ cells in the airways. We hypothesized that the newly characterized cytokine interleukin (IL)-16 is involved in the pathogenesis of asthma through its ability to selectively induce CD4+ cell recruitment within the inflamed bronchial wall. We investigated the expression of IL-16 in bronchial biopsies obtained from subjects with mild asthma (n = 10), atopic nonasthmatic individuals (n = 6), and normal control subjects (n = 10). Cryostat sections from 4% paraformaldehyde-fixed fiberoptic bronchial biopsies were immunostained using a specific antibody that recognizes human IL-16. IL-16 mRNA expression was determined by in situ hybridization. IL-16 immunoreactivity and mRNA were demonstrated mainly in bronchial epithelial cells in all subjects. IL-16 immunoreactivity and IL-16 mRNA expression within the epithelium were significantly higher in bronchial biopsies obtained from asthmatic subjects as compared to both atopic nonasthmatic and normal controls (P < 0.001). The numbers of subepithelial IL-16 immunoreactive cells and IL-16 mRNA-positive cells were also greater in the bronchial biopsies obtained from asthmatic subjects as compared to both atopic nonasthmatic and normal controls (P < 0.001). Epithelial expression of IL-16 immunoreactivity and mRNA correlated with the CD4+ cell infiltration (r2 = 0.70, P < 0.001). There were significant associations between epithelial and subepithelial IL-16 immunoreactivity and airway responsiveness to methacholine. This study demonstates that IL-16 is expressed in airway tissues, particularly in the epithelial cells, and that upregulation of its expression is a feature of allergic asthma. These results suggest an in vivo role for IL-16 in the pathogenesis of asthma, possibly through the recruitment of CD4+ cells, and support the increasing evidence for the participation of epithelial cells in regulating inflammatory responses.
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