In:
Allergy, Wiley, Vol. 55, No. 12 ( 2000-12), p. 1134-1141
Abstract:
Background: The cytokine network is thought to be essential in orchestrating airway inflammation in asthma. Although evidence has accumulated to suggest that atopic asthma is a Th2 disease, much less is known about nonatopic asthma. Methods: We have compared the production of IL‐4, IL‐6, IFN‐γ, and TNF‐α from peripheral blood leukocytes between atopic ( n =21) and nonatopic ( n =22) asthmatics and healthy nonatopic subjects ( n =20). Peripheral blood was incubated for 24 h either without stimulus or with LPS or PHA. Cytokines were measured by the immunotrapping technique (Dynamic Immunoassay). Results: When compared to healthy nonatopic subjects, both atopic and nonatopic asthmatics showed increased blood and sputum eosinophilia associated with raised total serum IgE levels. Similarly, both asthma groups displayed spontaneous, endotoxin‐induced overproduction of IL‐6. Enhanced spontaneous, endotoxin‐induced release of IL‐4 combined with reduced spontaneous IFN‐γ production was seen only in atopic asthma. In this group of patients, the production of IL‐4 was related to the extent of blood and sputum eosinophilia. In nonatopic asthmatics, serum levels of IgE were inversely related to the production of IFN‐γ. Conclusions: Both atopic and intrinsic asthma display raised blood and airway eosinophilia, raised total serum IgE, and overproduction of IL‐6 from peripheral blood. Atopic asthma is also characterized by impaired spontaneous release of IFN‐γ and increased production of IL‐4 that correlates with the magnitude of eosinophilic inflammation.
Type of Medium:
Online Resource
ISSN:
0105-4538
,
1398-9995
DOI:
10.1034/j.1398-9995.2000.00711.x
Language:
English
Publisher:
Wiley
Publication Date:
2000
detail.hit.zdb_id:
2003114-2
detail.hit.zdb_id:
391933-X
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