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ASTHMA |
1 Department of Paediatrics, Imperial College London at the Royal Brompton Hospital, London SW3 6NP, UK
2 Department of Gene Therapy, Imperial College London at the Royal Brompton Hospital, London SW3 6NP, UK
3 Department of Anaesthetics, Imperial College London at the Royal Brompton Hospital, London SW3 6NP, UK
Correspondence to:
Correspondence to:
Professor P K Jeffery
Lung Pathology, Royal Brompton Hospital, Sydney Street, London SW3 6NP, UK; p.jeffery{at}imperial.ac.uk
Background: The effective management and development of new treatments for children with difficult asthma requires investigation of the underlying airway pathology and its relationships with persistent symptoms and airflow limitation.
Methods: The density of immunologically distinct inflammatory cells and cells expressing interleukin (IL)-4, IL-5, and RANTES was determined in paraffin-embedded endobronchial biopsy specimens from 27 children with difficult asthma (616 years) following treatment with systemic corticosteroids. Eleven non-asthmatic children (716 years) acted as controls. Reticular basement membrane (RBM) thickness was also recorded and forced expiratory volume in 1 second (FEV1) and exhaled nitric oxide (FENO) measured, the latter in asthmatic children only.
Results: RBM thickness was greater in the asthmatic than the control group (median (range) 7.4 (3.111.1) v 5.1 (3.57.5) µm, p = 0.02). No other significant tissue difference was seen, nor was there a difference between asthmatic subjects with daily symptoms after systemic corticosteroids and those who became asymptomatic. CD4+ T lymphocyte density was higher in asthmatic subjects with persistent airflow limitation (post-bronchodilator FEV1<80% predicted) than in those without (9.1 (5.513.6) v 3.5 (0.634.9)%, p = 0.027). Analysing all asthmatic subjects together, there were negative correlations between CD4+ T lymphocytes and both pre-bronchodilator FEV1 (r = 0.57 (95% CI 0.79 to 0.23), p = 0.002) and post-bronchodilator FEV1 (r = 0.61 (95% CI 0.81 to 0.29), p<0.001). There were no significant correlations between FENO and inflammatory cells of any type.
Conclusion: In children with difficult asthma treated with systemic corticosteroids, persistent airflow limitation is associated with a greater density of CD4+ T lymphocytes in endobronchial biopsy specimens.
Abbreviations: FENO, exhaled nitric oxide; FEV1, forced expiratory volume in 1 second; PAL, persistent airflow limitation; RBM, reticular basement membrane
Keywords: bronchoscopy; endobronchial biopsy; T lymphocytes; immunopathology; asthma; children
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Thorax 2004 59: 821a.
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