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Pediatric severe asthma with fungal sensitization is mediated by steroid-resistant IL-33.
- Source :
-
The Journal of allergy and clinical immunology [J Allergy Clin Immunol] 2015 Aug; Vol. 136 (2), pp. 312-22.e7. Date of Electronic Publication: 2015 Mar 05. - Publication Year :
- 2015
-
Abstract
- Background: The mechanism underlying severe asthma with fungal sensitization (SAFS) is unknown. IL-33 is important in fungus-induced asthma exacerbations, but its role in fungal sensitization is unexplored.<br />Objective: We sought to determine whether fungal sensitization in children with severe therapy-resistant asthma is mediated by IL-33.<br />Methods: Eighty-two children (median age, 11.7 years; 63% male) with severe therapy-resistant asthma were included. SAFS (n = 38) was defined as specific IgE or skin prick test response positivity to Aspergillus fumigatus, Alternaria alternata, or Cladosporium herbarum. Clinical features and airway immunopathology were assessed. Chronic exposure to house dust mite and A alternata were compared in a neonatal mouse model.<br />Results: Children with SAFS had earlier symptom onset (0.5 vs 1.5 years, P = .006), higher total IgE levels (637 vs 177 IU/mL, P = .002), and nonfungal inhalant allergen-specific IgE. Significantly more children with SAFS were prescribed maintenance oral steroids (42% vs 14%, P = .02). SAFS was associated with higher airway IL-33 levels. In neonatal mice A alternata exposure induced higher serum IgE levels, pulmonary IL-33 levels, and IL-13(+) innate lymphoid cell (ILC) and TH2 cell numbers but similar airway hyperresponsiveness (AHR) compared with those after house dust mite exposure. Lung IL-33 levels, IL-13(+) ILC numbers, TH2 cell numbers, IL-13 levels, and AHR remained increased with inhaled budesonide during A alternata exposure, but all features were significantly reduced in ST2(-/-) mice lacking a functional receptor for IL-33.<br />Conclusion: Pediatric SAFS was associated with more oral steroid therapy and higher IL-33 levels. A alternata exposure resulted in increased IL-33-mediated ILC2 numbers, TH2 cell numbers, and steroid-resistant AHR. IL-33 might be a novel therapeutic target for SAFS.<br /> (Copyright © 2015 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Adolescent
Alternaria immunology
Animals
Animals, Newborn
Antibodies, Anti-Idiotypic therapeutic use
Antibodies, Monoclonal, Humanized therapeutic use
Aspergillus fumigatus immunology
Asthma complications
Asthma pathology
Child
Cladosporium immunology
Disease Models, Animal
Female
Humans
Immunoglobulin E genetics
Immunoglobulin E immunology
Interleukin-1 Receptor-Like 1 Protein
Interleukin-13 genetics
Interleukin-13 immunology
Interleukin-33
Interleukins genetics
Male
Mice
Mycoses complications
Mycoses pathology
Omalizumab
Pyroglyphidae chemistry
Pyroglyphidae immunology
Receptors, Interleukin deficiency
Receptors, Interleukin genetics
Receptors, Interleukin immunology
Severity of Illness Index
Skin Tests
Th2 Cells immunology
Th2 Cells pathology
Anti-Asthmatic Agents therapeutic use
Asthma drug therapy
Asthma immunology
Budesonide therapeutic use
Interleukins immunology
Mycoses drug therapy
Mycoses immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1097-6825
- Volume :
- 136
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- The Journal of allergy and clinical immunology
- Publication Type :
- Academic Journal
- Accession number :
- 25746970
- Full Text :
- https://doi.org/10.1016/j.jaci.2015.01.016