IL‐5, IL‐8 and GM‐CSF immunostaining of sputum cells in bronchial asthma and chronic bronchitis
- 1 August 1995
- journal article
- Published by Wiley in Clinical and Experimental Allergy
- Vol. 25 (8) , 720-728
- https://doi.org/10.1111/j.1365-2222.1995.tb00009.x
Abstract
Background: Granulocyte‐macrophage colony stimulating factor (GM‐CSF) and inlerleukin (IL)‐5 or IL‐8 have been .suggested to play an important role in the pathogenesis of eosinophilic airway inflammation in bronchial asthma or neutrophilic airway inflammation in chronic bronchitis, respectively, However, GM‐CSF and IL‐8 have biological activities to either eosinophils or neutrophils. Objective: To investigate the contribution of these cytokines to airway inflammation, we compared the cellular differential and immunolocalization of GM‐CSF, IL‐5 and IL‐8 in sputum cells from patients with bronchial asthma and chronic bronchitis. Methods: Cytospins of sputum cells from 12 patients with bronchial asthma and 12 with chronic bronchitis were subjected to cellular differential counting and immunocytochemistry with antihuman GM‐CSF, IL‐5 and IL‐8 antibody. Results: The predominant cells in bronchial asthma were eosinophils and lymphocytes, while those in chronic bronchitis were neutrophils. All cytokines examined were detected in either bronchial asthma or chronic bronchitis, although the percentage of GM‐CSF and IL‐5 positive cells in bronchial asthma (53.4 ± 6.0 [mean±sfm]% and 9.7 ± 2.8%, respectively) was significantly higher than that in chronic bronchitis (11.4±2.5%; P < 0.001 and 1.7plusmn;0.3%; P < 0.007. respectively). In contrast, the percentage of IL‐8 positive cells in chronic bronchitis (23.8 ± 7.0%) was significantly higher than that in bronchial asthma (7.7 ± 1.9%; P < 0.04). The cells positive for IL‐5 were lymphocytes in bronchial asthma and chronic bronchitis. The cells positive for GM‐CSF in bronchial asthma were predominantly eosinophils. while those in chronic bronchitis were monocytes/macrophages and neutrophils. In contrast, neutrophils are mainly positive for IL‐8 in chronic bronchitis, while monocytes/macrophages and bronchial epithelial cells are positive for IL‐8 in bronchial asthma. Conclusion: The immunochcmical comparison of GM‐CSF and IL‐8 localization in sputum cells between bronchial asthma chronic bronchitis suggests the differential regulation and roles of these cytokines in eosinophilic vs neutrophilic airway inflammation, resulting in the development of different types of airway inflammation.Keywords
This publication has 31 references indexed in Scilit:
- Differential in situ cytokine gene expression in acute versus chronic atopic dermatitis.Journal of Clinical Investigation, 1994
- Eosinophilic and neutrophilic inflammation in asthma, chronic bronchitis, and chronic obstructive pulmonary diseaseJournal of Allergy and Clinical Immunology, 1993
- Upregulation of formyl-peptide and interleukin-8—induced eosinophil chemotaxis in patients with allergic asthmaJournal of Allergy and Clinical Immunology, 1993
- Predominant TH2-like Bronchoalveolar T-Lymphocyte Population in Atopic AsthmaNew England Journal of Medicine, 1992
- Use of induced sputum cell counts to investigate airway inflammation in asthma.Thorax, 1992
- Endobronchial allergen challenge in asthma. Demonstration of cellular source of granulocyte macrophage colony-stimulating factor by in situ hybridization.Journal of Clinical Investigation, 1991
- Highly purified murine interleukin 5 (IL-5) stimulates eosinophil function and prolongs in vitro survival. IL-5 as an eosinophil chemotactic factor.The Journal of Experimental Medicine, 1988
- Recombinant human interleukin 5 is a selective activator of human eosinophil function.The Journal of Experimental Medicine, 1988
- Recombinant human granulocyte-macrophage colony-stimulating factor stimulates in vitro mature human neutrophil and eosinophil function, surface receptor expression, and survival.Journal of Clinical Investigation, 1986
- Response of intrapulmonary chemoreceptors in the duck to changes in PCO2 and pHRespiration Physiology, 1978