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Comparison of inflammatory cell counts in asthma: induced sputum vs bronchoalveolar lavage and bronchial biopsies
Author(s) -
GROOTENDORST D. C.,
SONT J. K.,
WILLEMS L. N. A.,
KLUINNELEMANS J. C.,
KRIEKEN J. H. J. M.,
VESELICCHARVAT M.,
STERK P. J.
Publication year - 1997
Publication title -
clinical and experimental allergy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 154
eISSN - 1365-2222
pISSN - 0954-7894
DOI - 10.1046/j.1365-2222.1997.890900.x
Subject(s) - bronchoalveolar lavage , sputum , medicine , hypertonic saline , asthma , methacholine , eosinophil , pathology , bronchus , respiratory disease , bronchoscopy , gastroenterology , immunology , lung , tuberculosis
Summary Background Induced sputum potentially allows monitoring of airway inflammation in patients with asthma in a non‐invasive way. However, the relationship between the cellular content in sputum and airway tissue has not been fully clarified. Objective We compared the cellular compositions of hypertonic saline‐induced sputum, bronchoalveolar lavage fluid (BAL) and bronchial biopsies in 18 clinically stable patients with mild to moderate atopic asthma (baseline FEV 1 : range 61–114%pred, PC 20 methacholine: 0.04–4.7 mg/mL). They were treated with inhaled short‐acting bronchodilators on demand, with ( n = 8) or without ( n = 10) regular inhaled steroids. Methods Each patient underwent sputum induction and fiberoptic bronchoscopy on separate days in random order. Differential cell counts of induced sputum, bronchoalveolar lavage and bronchial wash were determined on May‐Grünwald‐Giemsa stained cytospins. Flow cytometry was performed on sputum and BAL samples. Immunohistochemical techniques were used to stain inflammatory cells in 6 μm cryostat sections of bronchial biopsies. Results Sputum cell differentials were not different between the patients with and without inhaled steroids, and showed a median value of 19.4% squamous cells, with 1.0% eosinophils, 3.3% lymphocytes, 28.7% neutrophils, 49.4% macrophages and 6.9% cylindric epithelial cells (in percentage non‐squamous cells). The percentage eosinophils in sputum was significantly correlated with their percentage in bronchial wash( R s = 0.52, P = 0.03) and in BAL ( R s = 0.55, P = 0.02), whilst there was a trend towards such a correlation between the number of eosinophils/mL sputum and the number of EG2 + eosinophils/mm 2 lamina propria in bronchial biopsies ( R s = 0.44, P = 0.07). In addition, the percentage of CD4 + lymphocytes correlated between sputum and BAL ( R s = 0.55, P = 0.03). Conclusion We conclude that the eosinophil counts in hypertonic saline‐induced sputum from patients with asthma are related to those in bronchial wash and BAL and, to a lesser extent, with the counts in bronchial biopsies. This suggests that induced sputum can be used to monitor the presence and severity of airway inflammation in asthma.