Literature DB >> 11112154

Inflammation and structural changes in the airways of patients with atopic and nonatopic asthma. BHR Group.

K Amin1, D Lúdvíksdóttir, C Janson, O Nettelbladt, E Björnsson, G M Roomans, G Boman, L Sevéus, P Venge.   

Abstract

The aim of the present study was to compare the cellular pattern and structural changes in the airway walls of atopic and nonatopic patients with asthma. Bronchial biopsy specimens were obtained from 13 atopic subjects with asthma, nine nonatopic patients with asthma, and seven healthy control subjects and investigated using immunohistochemical methods. The number of eosinophils increased in both asthma groups, but significantly more in the atopic group. The number of mast cells increased similarly in the two asthma groups, whereas the number of neutrophils increased only in the nonatopic asthma group. The number of T-lymphocytes (CD3-, CD4-, CD8-, CD-25-positive cells) was higher in patients with atopic asthma compared with nonatopic asthma. Interleukin-4 (IL-4) and IL-5-positive cells were more frequently found in the atopic asthma group, whereas cells staining for IL-8 were more frequent in the nonatopic group. The degree of epithelial damage was significantly higher in the atopic asthma group compared with the control subjects and the nonatopic asthmatics. The tenascin and laminin layer was significantly thicker in the atopic group compared with the group of nonatopic asthmatics. In the atopic group, there was a significant negative correlation between epithelial integrity (defined as the relative length of intact epithelium) and the eosinophil count and also between the number of CD25-positive cells and epithelial integrity. The number of mast cells correlated positively with the thickness of tenascin- and laminin-positive layers. In conclusion, we provide evidence of different patterns of involvement of inflammatory cells in atopic and nonatopic patients with asthma. There were also structural differences in the bronchial mucous membrane between atopic asthma and nonatopic asthma. This suggests that there are differences in the extent of the immunopathologic response of these clinically distinct forms of asthma.

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Year:  2000        PMID: 11112154     DOI: 10.1164/ajrccm.162.6.9912001

Source DB:  PubMed          Journal:  Am J Respir Crit Care Med        ISSN: 1073-449X            Impact factor:   21.405


  68 in total

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Authors:  K Amin; A Ekberg-Jansson; C-G Löfdahl; P Venge
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Review 2.  Variability of inflammatory cell counts on bronchial biopsies of normal subjects.

Authors:  H Turcotte; M Laviolette; M Boutet; L-P Boulet
Journal:  Lung       Date:  2003       Impact factor: 2.584

Review 3.  Eosinophils: important players in humoral immunity.

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4.  Inflammation of bronchial smooth muscle in allergic asthma.

Authors:  H Begueret; P Berger; J M Vernejoux; L Dubuisson; R Marthan; J M Tunon-de-Lara
Journal:  Thorax       Date:  2007-01       Impact factor: 9.139

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Journal:  Blood       Date:  2006-12-29       Impact factor: 22.113

6.  Relationship between exposure to domestic allergens and bronchial hyperresponsiveness in non-sensitised, atopic asthmatic subjects.

Authors:  S J Langley; S Goldthorpe; M Craven; A Woodcock; A Custovic
Journal:  Thorax       Date:  2005-01       Impact factor: 9.139

7.  Quercetin blocks airway epithelial cell chemokine expression.

Authors:  Suparna Nanua; Suzanna M Zick; Juan E Andrade; Umadevi S Sajjan; John R Burgess; Nicholas W Lukacs; Marc B Hershenson
Journal:  Am J Respir Cell Mol Biol       Date:  2006-06-22       Impact factor: 6.914

Review 8.  Allergic Respiratory Inflammation and Remodeling.

Authors:  Kawa A M Amin
Journal:  Turk Thorac J       Date:  2015-07-01

Review 9.  The airway epithelium: soldier in the fight against respiratory viruses.

Authors:  Marjolaine Vareille; Elisabeth Kieninger; Michael R Edwards; Nicolas Regamey
Journal:  Clin Microbiol Rev       Date:  2011-01       Impact factor: 26.132

10.  The role of tenascin-C in tissue injury and tumorigenesis.

Authors:  Kim S Midwood; Gertraud Orend
Journal:  J Cell Commun Signal       Date:  2009-10-17       Impact factor: 5.782

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