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Eosinophils are a feature of upper and lower airway pathology in non-atopic asthma, irrespective of the presence of rhinitis
Background Asthma and rhinitis often co‐exist and there are data to suggest that they may be two ends of the same disease spectrum. Immunohistochemical studies have shown that eosinophilia in the airways is a feature of rhinitic patients without asthma. Objective The aim of our study was to examine...
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Published in: | Clinical and experimental allergy 2000-05, Vol.30 (5), p.663-669 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Background
Asthma and rhinitis often co‐exist and there are data to suggest that they may be two ends of the same disease spectrum. Immunohistochemical studies have shown that eosinophilia in the airways is a feature of rhinitic patients without asthma.
Objective
The aim of our study was to examine whether cellular infiltration exists in the nasal mucosa of asthmatics even in the absence of symptoms and signs of rhinitis.
Methods
Nasal mucosa biopsies were taken from 27 non‐atopic subjects and comprised nine asthmatic rhinitic patients (AR), eight asthmatic non‐rhinitic patients (ANR) and 10 healthy control subjects (N). Bronchial mucosa biopsies were also taken simultaneously from some of the patients (n = 10) to determine whether there was an association between cellular infiltration in the nose and the lungs. The alkaline phosphatase‐anti‐alkaline phosphatase (APAAP) method was used on 6 μm thick cryostat sections using monoclonal antibodies against T cells (CD4, CD8), eosinophils (EG2) and mast cells (mast cell tryptase). Slides were counted blind and results expressed as cells per field.
Results
The results showed that eosinophil counts were higher in both asthma groups compared with control nasal biopsies (median values AR 8.3, ANR 9.2, N 2.1 cells per field, P |
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ISSN: | 0954-7894 1365-2222 |
DOI: | 10.1046/j.1365-2222.2000.00804.x |