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Vaccination against IL-33 Inhibits Airway Hyperresponsiveness and Inflammation in a House Dust Mite Model of Asthma
Uppsala University, Disciplinary Domain of Science and Technology, Biology, Department of Cell and Molecular Biology.
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2015 (English)In: PLoS ONE, ISSN 1932-6203, Vol. 10, no 7, e0133774Article in journal (Refereed) Published
Abstract [en]

In several clinical and experimental studies IL-33 and its receptor have been found to play important roles in the development of asthma and allergic airway inflammation. We evaluated the effects of vaccination against IL-33 in a mouse model of airway inflammation induced by house dust mite (HDM) allergen. Balb/c mice received the IL-33 vaccine subcutaneously, followed by intranasal administration of HDM for up to six weeks. Vaccination against IL-33 induced high titers of specific anti-IL-33 IgG antibodies that inhibited HDM-induced airway hyperresponsiveness (AHR) in the conducting airways and tissue damping. The vaccination also attenuated the HDM-induced elevation in the numbers of eosinophils in bronchoalveolar lavage fluid (BALF) and suppressed the accumulation of inflammatory cells in the airways. Furthermore, the levels of IL-17A, IL-25, IL-33 and TSLP in lung tissue homogenates were reduced by vaccination against IL-33. These observations demonstrate that vaccination against IL-33 inhibits HDM-induced development of AHR, airway inflammation and production of inflammatory cytokines. The results also indicate an important role of IL-33 in the regulation of AHR of the distal lung compartments. Thus, administration of such a vaccine is potentially an effective therapeutic tool for treating allergic asthma.

Place, publisher, year, edition, pages
2015. Vol. 10, no 7, e0133774
National Category
Clinical Medicine
URN: urn:nbn:se:uu:diva-260840DOI: 10.1371/journal.pone.0133774ISI: 000358594300032PubMedID: 26214807OAI: diva2:848627
Swedish Research Council, 521-2011-3286 521-2011-2517
Available from: 2015-08-25 Created: 2015-08-25 Last updated: 2015-08-25Bibliographically approved

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