Spleen tyrosine kinase inhibition attenuates airway hyperresponsiveness and pollution-induced enhanced airway response in a chronic mouse model of asthma

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

卷:131

Article

Penton, Patricia Castellanos¹  Wang, Xiaomin¹  Amatullah, Hajera^2,3  Cooper, Josephine⁴  Godri, Krystal⁴  North, Michelle L.^1,2,3  Khanna, Nivedita^1,2,3  Scott, Jeremy A.⁵  Chow, Chung-Wai^1,4,6 

[1] Univ Toronto, Fac Med, Dept Med, Div Respirol, Toronto, ON M5G 1L7, Canada

[2] Univ Toronto, Fac Med, Dalla Lana Sch Publ Hlth, Div Occupat & Environm Hlth, Toronto, ON M5G 1L7, Canada

[3] Univ Toronto, Gage Occupat & Environm Hlth Unit, Toronto, ON M5G 1L7, Canada

[4] Univ Toronto, Fac Sci Appl, So Ontario Ctr Atmospher Aerosol Res, Toronto, ON M5G 1L7, Canada

[5] Lakehead Univ, Dept Hlth Sci, Thunder Bay, ON P7B 5E1, Canada

[6] Univ Hlth Network, Multiorgan Transplant Programme, Toronto, ON, Canada

关键词: Airways hyperresponsiveness;    Syk;    asthma;    pollution;    mouse;   

DOI  :  10.1016/j.jaci.2012.07.039

来源: Elsevier

【 摘 要 】

Background: Asthma is a chronic inflammatory disease characterized by airways hyperresponsiveness (AHR), reversible airflow obstruction, airway remodeling, and episodic exacerbations caused by air pollutants, such as particulate matter (PM; PM <2.5 mu m in diameter [PM2.5]) and ozone (O-3). Spleen tyrosine kinase (Syk), an immunoregulatory kinase, has been implicated in the pathogenesis of asthma. Objective: We sought to evaluate the effect of Syk inhibition on AHR in a chronic mouse model of allergic airways inflammation and pollutant exposure. Methods: We used a 12-week chronic ovalbumin (OVA) sensitization and challenge mouse model of airways inflammation followed by exposure to PM2.5 plus O-3. Respiratory mechanics and methacholine (MCh) responsiveness were assessed by using the flexiVent system. The Syk inhibitor NVP-QAB-205 was nebulized intratracheally by using a treatment-based protocol 15 minutes before assessment of MCh responsiveness. Results: Syk expression increased significantly in the airway epithelia of OVA-sensitized and OVA-challenged (OVA/OVA) mice compared with OVA-sensitized but PBS-challenged (OVA/PBS) control mice. OVA/OVA mice exhibited AHR to MCh, which was attenuated by a single administration of NVP-QAB-205 (0.3 and 3 mg/kg). PM2.5 plus O-3 significantly augmented AHR to MCh in the OVA/OVA mice, which was abrogated by NVP-QAB-205. Total inflammatory cell counts were significantly higher in the bronchoalveolar lavage fluid from OVA/OVA than OVA/PBS mice and were unaffected by PM2.5 plus O-3 or NVP-QAB-205. Conclusion: NVP-QAB-205 reduced AHR and the enhanced response to PM2.5 plus O-3 to normal levels in an established model of chronic allergic airways inflammation, suggesting that Syk inhibitors have promise as a therapy for asthma. (J Allergy Clin Immunol 2013;131:512-20.)

【 授权许可】

Free