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Published on: August 7, 2017
Local and systemic immunological parameters associated with remission of asthma symptoms in children
Susan Waserman1, Parameswaran Nair, Denis Snider
1Departments of Medicine, McMaster University, Hamilton, ON, Canada. waserman@mcmaster.ca.
Insights
Asthma remission is linked to reduced eosinophilic inflammation and lower type 1 cytokine production. These changes in immunological and clinical markers may explain why some children outgrow their asthma symptoms.
Area of Science:
- Immunology
- Pulmonology
- Allergy
Background:
- Asthma remission triggers are not well understood.
- Investigating immunological and clinical factors in childhood asthma resolution is crucial.
Purpose of the Study:
- To examine cytokine and mediator changes in resolving asthma (RA) versus persistent asthma (CA) and controls.
- To identify immunological markers associated with asthma symptom resolution in adolescents.
Main Methods:
- Compared clinical parameters, sputum eosinophils, and peripheral blood mononuclear cell (PBMC) cytokine production in three adolescent groups: CA, RA, and controls.
- Assessed methacholine airway hyperresponsiveness, sputum eosinophilic cationic protein (ECP), and Interleukin-5 (IL-5).
Main Results:
- Continuing asthma (CA) subjects exhibited higher airway hyperresponsiveness, sputum eosinophils, ECP, and IL-5 compared to resolving asthma (RA) subjects.
- CA group showed increased production of type 1 cytokines (IL-12, IFN-γ, TNF-α) from PBMCs, while IL-4 and IL-5 levels were similar between CA and RA groups.
- Resolving asthma (RA) was associated with reduced eosinophilic inflammation and lower type 1 cytokine expression.
Conclusions:
- Decreased type 1 cytokine expression and reduced eosinophilic inflammation are associated with asthma symptom resolution.
- These findings offer insights into the immunological mechanisms underlying asthma remission in adolescents.
Abstract:
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.
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