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Local and systemic immunological parameters associated with remission of asthma symptoms in children

The immunological and clinical parameters that are associated with asthma remission are poorly understood. The cytokine and local mediator changes associated with the resolution of asthma symptoms were examined in three groups of subjects 12-18 years of age (n = 15 in each group): (a) continuing ast...

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Published in:Allergy, asthma, and clinical immunology asthma, and clinical immunology, 2012-10, Vol.8 (1), p.16-16, Article 16
Main Authors: Waserman, Susan, Nair, Parameswaran, Snider, Denis, Conway, Mary, Jayaram, Lata, McCleary, Lynn M, Dolovich, Jerry, Hargreave, Frederick E, Marshall, Jean S
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Language:English
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Summary:The immunological and clinical parameters that are associated with asthma remission are poorly understood. The cytokine and local mediator changes associated with the resolution of asthma symptoms were examined in three groups of subjects 12-18 years of age (n = 15 in each group): (a) continuing asthma group (CA) who had persistent symptoms since early childhood, (b) an age, sex and atopic status-matched group who had persistent symptoms in early childhood but in whom these had resolved (RA), and (c) a non-atopic, non-asthmatic control group. Clinical parameters, sputum cell counts, peripheral blood mononuclear cell (PBMC) cytokine production and activation marker expression were determined. All of the CA had methacholine airway hyperresponsiveness compared with only half of the RA subjects. The CA showed elevated numbers of eosinophils and increased ECP and IL-5 in sputum, which were not observed in the RA. PBMC cytokine studies revealed increased production of the type 1 cytokines IL-12, IFN-γ and TNF-α in the CA group compared with the RA group, under a range of activation conditions, however, the production of IL-4 and IL-5 were unchanged. These findings suggest that decreased type 1 cytokine expression as well as decreased eosinophilic inflammation is associated with the resolution of asthma symptoms.
ISSN:1710-1492
1710-1484
1710-1492
DOI:10.1186/1710-1492-8-16