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Effects of,Interleukin-9 Blockade on Chronic Airway Inflammation in Murine Asthma Models

Authors
Kim, Myung ShinCho, Kyung-AhCho, Young JooWoo, So-Youn
Issue Date
Jul-2013
Publisher
대한천식알레르기학회
Keywords
Interleukin-9; allergic asthma; T helper 17; anti-interleukin-9 antibody
Citation
Allergy, Asthma & Immunology Research, v.5, no.4, pp 197 - 206
Pages
10
Journal Title
Allergy, Asthma & Immunology Research
Volume
5
Number
4
Start Page
197
End Page
206
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/13556
DOI
10.4168/aair.2013.5.4.197
ISSN
2092-7355
2092-7363
Abstract
Purpose: Asthma is a chronic inflammatory disease of the airways associated with structural changes and airway remodeling. Interleukin (IL)-9 has pleiotropic effects on both inflammatory cells and airway structural cells, which are involved in asthma pathogenesis. We evaluated the effects of IL-9 blockade on chronic airway inflammation. Methods: Acute airway inflammation was induced in Balb/c mice using aerosolized ovalbumin (OVA), whereas chronic asthma was induced by OVA exposure for 5 weeks with anti-IL-9 or isotype-matched antibody (Ab) treatment during the OVA challenge. Inflammatory cells in bronchoalveolar lavage fluid (BALE) were counted and lung tissues were stained to detect cellular infiltration, mucus deposition, and collagen accumulation. The levels of interferon (IFN)-gamma, IL-4, IL-5, IL-9, IL-17, and immunoglobulin E (IgE) in BALE were measured using enzyme linked immunosorbent assays, and profiles of inflammatory cells and subsets of T helper (Th) cells were analyzed using flow cytometry. Results: IL-9, IL-17, and IFN-gamma levels were significantly increased in the chronic group compared to the acute asthma group. However, the number of IL-9-positive cells was not affected, with a decrease in Th17 cells in OVA-challenged caspase-1 knockout mice. Numbers of eosinophils, neutrophils, B cells, mast cells, and Th17 cells decreased after administration of anti-IL-9 Ab. Total IgE, IL-5, IL-9, and IL-17 levels were also lower in the anti-IL-9 group. Conclusions: Our results suggest that anti-IL-9 Ab treatment inhibits pulmonary infiltration of inflammatory cells and cytokine production, especially IL-17. These results provide a basis for the use of an anti-IL-9 Ab to combat IL-17-mediated airway inflammation.
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