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- Title
Annexin-A1-Derived Peptide Ac2-26 Suppresses Allergic Airway Inflammation and Remodelling in Mice.
- Authors
Ferreira, Tatiana Paula Teixeira; Guimarães, Fernanda Verdini; Sá, Yago Amigo Pinho Jannini; da Silva Ribeiro, Natalia Barreto; de Arantes, Ana Carolina Santos; de Frias Carvalho, Vinicius; Sousa, Lirlândia Pires; Perretti, Mauro; Martins, Marco Aurélio; e Silva, Patrícia Machado Rodrigues
- Abstract
Annexin-A1 (AnxA1) and its N-terminal derived peptide Ac2-26 regulate the inflammatory response in several experimental models of disorders. This study evaluated the effect of endogenous AnxA1 and its N-terminal peptide Acetyl 2-26 (Ac2-26) on allergic asthma triggered by house dust mite (HDM) extract in mice. ANXA1−/− and wildtype (WT) mice were exposed to intranasal instillation of HDM every other day for 3 weeks, with analyses performed 24 h following the last exposure. Intranasal administration of peptide Ac2-26 was performed 1 h before HDM, beginning 1 week after the initial antigen application. ANXA1−/− mice stimulated with HDM showed marked exacerbations of airway hyperreactivity (AHR), eosinophil accumulation, subepithelial fibrosis, and mucus hypersecretion, all parameters correlating with overexpression of cytokines (IL-4, IL-13, TNF-α, and TGF-β) and chemokines (CCL11/eotaxin-1 and CCL2/MCP-1). Intranasal treatment with peptide Ac2-26 decreased eosinophil infiltration, peribronchiolar fibrosis, and mucus exacerbation caused by the allergen challenge. Ac2-26 also inhibited AHR and mediator production. Collectively, our findings show that the AnxA1-derived peptide Ac2-26 protects against several pathological changes associated with HDM allergic reaction, suggesting that this peptide or related AnxA1-mimetic Ac2-26 may represent promising therapeutic candidates for the treatment of allergic asthma.
- Subjects
PEPTIDES; HOUSE dust mites; PATHOLOGICAL physiology; INTRANASAL administration; AIRWAY (Anatomy)
- Publication
Cells (2073-4409), 2022, Vol 11, Issue 5, p759
- ISSN
2073-4409
- Publication type
Article
- DOI
10.3390/cells11050759