免疫学
蛋白酵素
过敏性炎症
炎症
免疫系统
细胞因子
过敏原
免疫
过敏
生物
酶
生物化学
作者
Corinne Cayrol,Anaïs Duval,Pauline Schmitt,Stéphane Roga,Mylène Camus,Alexandre Stella,Odile Burlet‐Schiltz,Anne Gonzalez de Peredo,Jean‐Philippe Girard
标识
DOI:10.1038/s41590-018-0067-5
摘要
Allergic inflammation has crucial roles in allergic diseases such as asthma. It is therefore important to understand why and how the immune system responds to allergens. Here we found that full-length interleukin 33 (IL-33FL), an alarmin cytokine with critical roles in type 2 immunity and asthma, functioned as a protease sensor that detected proteolytic activities associated with various environmental allergens across four kingdoms, including fungi, house dust mites, bacteria and pollens. When exposed to allergen proteases, IL-33FL was rapidly cleaved in its central 'sensor' domain, which led to activation of the production of type 2 cytokines in group 2 innate lymphoid cells. Preventing cleavage of IL-33FL reduced allergic airway inflammation. Our findings reveal a molecular mechanism for the rapid induction of allergic type 2 inflammation following allergen exposure, with important implications for allergic diseases.
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