- Author:
Jiu Yao WANG
1
Author Information
- Publication Type:Review
- Keywords: House dust mites; innate immunity; toll-like receptors; C-type lectin receptors; dendritic cells
- MeSH: Adolescent; Allergens; Asthma; Child; Dendritic Cells; Dust; Humans; Hydrazines; Hypersensitivity; Immunity, Innate; Immunoglobulin E; Inflammation; Lectins, C-Type; Mites; Peptide Hydrolases; Pyroglyphidae; Risk Factors; Th2 Cells; Toll-Like Receptors
- From:Allergy, Asthma & Immunology Research 2013;5(2):68-74
- CountryRepublic of Korea
- Language:English
- Abstract: Hypersensitivity to house dust mite (HDM; Dermatophagoides sp.) allergens is one of the most common allergic responses, affecting up to 85% of asthmatics. Sensitization to indoor allergens is the strongest independent risk factor associated with asthma. Additionally, >50% of children and adolescents with asthma are sensitized to HDM. Although allergen-specific CD4+ Th2 cells orchestrate the HDM allergic response through induction of IgE directed toward mite allergens, activation of innate immunity also plays a critical role in HDM-induced allergic inflammation. This review highlights the HDM components that lead to activation of the innate immune response. Activation may due to HDM proteases. Proteases may be recognized by protease-activation receptors (PARs), Toll-like receptors (TLRs), or C-type lectin receptors (CTRs), or act as a molecular mimic for PAMP activation signaling pathways. Understanding the role of mite allergen-induced innate immunity will facilitate the development of therapeutic strategies that exploit innate immunity receptors and associated signaling pathways for the treatment of allergic asthma.