Department of Experimental Medicine, University of Perugia, 06132 Perugia, Italy.
European Institute for Research in Cystic Fibrosis, San Raffaele Scientific Institute, Milan, Italy.
Cell Rep. 2017 Aug 15;20(7):1667-1680. doi: 10.1016/j.celrep.2017.07.063.
The interleukin 17 (IL-17) cytokine and receptor family is central to antimicrobial resistance and inflammation in the lung. Mice lacking IL-17A, IL-17F, or the IL-17RA subunit were compared with wild-type mice for susceptibility to airway inflammation in models of infection and allergy. Signaling through IL-17RA was required for efficient microbial clearance and prevention of allergy; in the absence of IL-17RA, signaling through IL-17RC on epithelial cells, predominantly by IL-17F, significantly exacerbated lower airway Aspergillus or Pseudomonas infection and allergic airway inflammation. In contrast, following infection with the upper respiratory pathogen Staphylococcus aureus, the IL-17F/IL-17RC axis mediated protection. Thus, IL-17A and IL-17F exert distinct biological effects during pulmonary infection; the IL-17F/IL-17RC signaling axis has the potential to significantly worsen pathogen-associated inflammation of the lower respiratory tract in particular, and should be investigated further as a therapeutic target for treating pathological inflammation in the lung.
白细胞介素 17(IL-17)细胞因子和受体家族是肺部抗微生物和炎症反应的核心。为了研究气道炎症易感性,我们将缺乏白细胞介素 17A(IL-17A)、白细胞介素 17F(IL-17F)或白细胞介素 17RA 亚单位的小鼠与野生型小鼠进行了比较,这些小鼠存在感染和过敏模型。通过 IL-17RA 的信号传递对于有效的微生物清除和预防过敏是必需的;在缺乏 IL-17RA 的情况下,上皮细胞通过 IL-17F 主要通过 IL-17RC 进行信号传递,显著加重了气道曲霉菌或铜绿假单胞菌感染和过敏气道炎症。相比之下,在上呼吸道病原体金黄色葡萄球菌感染后,IL-17F/IL-17RC 轴介导了保护作用。因此,IL-17A 和 IL-17F 在肺部感染期间发挥了不同的生物学作用;IL-17F/IL-17RC 信号轴有可能特别显著地加重下呼吸道与病原体相关的炎症,应进一步作为治疗肺部病理性炎症的治疗靶点进行研究。