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IL-17F/IL-17RC 轴促进近端气道的呼吸性过敏。

The IL-17F/IL-17RC Axis Promotes Respiratory Allergy in the Proximal Airways.

机构信息

Department of Experimental Medicine, University of Perugia, 06132 Perugia, Italy.

European Institute for Research in Cystic Fibrosis, San Raffaele Scientific Institute, Milan, Italy.

出版信息

Cell Rep. 2017 Aug 15;20(7):1667-1680. doi: 10.1016/j.celrep.2017.07.063.

Abstract

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.

摘要

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。

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