单位：[1]Department of Surgical Intensive Care Unit, Beijing An Zhen Hospital, Capital Medical University, Beijing, China首都医科大学附属安贞医院[2]Department of Pulmonary and Critical Care Medicine, Center for Respiratory Diseases, China-Japan Friendship Hospital, National Clinical Research Center for Respiratory Diseases, Beijing, China
Objectives Interleukin (IL)-25, IL-33, and thymic stromal lymphopoietin (TSLP) are the important drivers for excessive type-2 immunity. It has been well elucidated that IL-25/IL-33/TSLP plays an important role in allergic airway inflammation and remodeling, whereas their roles in idiopathic pulmonary fibrosis (IPF) still remained largely unclear. Herein, the aim of the review is to discuss the potential role and mechanism of IL-25/IL-33/TSLP on IPF by literature analysis and summary. Data source We have done a literature search using the following terms: ("idiopathic pulmonary fibrosis" OR "IPF" OR "lung fibrosis") and (TSLP or "thymic stromal lymphopoietin" or IL-25 OR IL-17E OR IL-33) from the database of PubMed published in English up to July 2018. Study selection We have totally found 58 articles by using the retrieval terms mentioned above. By careful title and abstract reading, 10 original research articles of high quality were enrolled for the full text reading and analysis. Two additional relevant studies were also included during the course of literature readings. Results IL-25/IL-33/TSLP and their corresponding receptors, that is, IL-17BR/ST2L/TSLPR, are shown to be up-regulated both in IPF patients and bleomycin (BLM)-induced lung fibrosis mice model. IL-25 may promote lung fibrosis by activating IL-17BR+fibroblast and IL-17BR+ILC2 (type 2 innate lymphoid cell). Full length (fl)-IL-33, as a transcription factor mainly in the cell nucleus, mediated non-atopic lung inflammation and fibrosis by modulating expressions of several pro-fibrotic mediators, including transforming growth factor (TGF)-b1. By contrast, mature (m)-IL-33 potentiates lung fibrosis by recruiting ST2L+M2 macrophages and ST2L+ILC2 to enlarge type 2 immunity. TSLP was shown to directly promote CCL2 expression in primary human lung fibroblasts (pHLFs). Conclusion IL-25/IL-33/TSLP contributes to non-allergic lung fibrosis by mediating persistent abnormal epithelial-mesenchymal crosstalk. IL-25/IL-33/TSLP may serve the promising novel target for the treatment of IPF.
基金：
Science Foundation initiated by Capital
Medical University (PYZ2017024).
第一作者单位：[1]Department of Surgical Intensive Care Unit, Beijing An Zhen Hospital, Capital Medical University, Beijing, China
通讯作者：
通讯机构：[1]Department of Surgical Intensive Care Unit, Beijing An Zhen Hospital, Capital Medical University, Beijing, China[2]Department of Pulmonary and Critical Care Medicine, Center for Respiratory Diseases, China-Japan Friendship Hospital, National Clinical Research Center for Respiratory Diseases, Beijing, China[*1]Department of Pulmonary and Critical Care Medicine, China-Japan Friendship Hospital, No. 2 YinghuaEast Road, Beijing 100029, China.[*2]Department of Surgical Intensive Care Unit, Beijing An Zhen Hospital, Capital Medical University, No. 2 Anzhen Rd., Chang- Yang District, Beijing 100029, China.
推荐引用方式(GB/T 7714)：
Xu Xuefeng,Dai Huaping,Zhang Jinglan.The potential role of interleukin (IL)-25/IL-33/thymic stromal lymphopoietin (TSLP) on the pathogenesis of idiopathic pulmonary fibrosis[J].CLINICAL RESPIRATORY JOURNAL.2022,doi:10.1111/crj.13541.
APA：
Xu, Xuefeng,Dai, Huaping&Zhang, Jinglan.(2022).The potential role of interleukin (IL)-25/IL-33/thymic stromal lymphopoietin (TSLP) on the pathogenesis of idiopathic pulmonary fibrosis.CLINICAL RESPIRATORY JOURNAL,,
MLA：
Xu, Xuefeng,et al."The potential role of interleukin (IL)-25/IL-33/thymic stromal lymphopoietin (TSLP) on the pathogenesis of idiopathic pulmonary fibrosis".CLINICAL RESPIRATORY JOURNAL .(2022)
