Triptolide alleviates allergic airway inflammation by inhibiting group 2 innate lymphoid cell function

IF 4.7 2区 医学 Q2 IMMUNOLOGY International immunopharmacology Pub Date : 2025-02-06 Epub Date: 2025-01-06 DOI:10.1016/j.intimp.2024.113989
Chenghua Yan , Wendong Kuang , Xinsheng Liu
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Abstract

Group 2 innate lymphoid cells (ILC2s) produce the type 2 cytokines IL-5 and IL-13 and contribute to type 2 immune responses, such as allergic airway inflammation. However, specific drugs, especially traditional Chinese medicines, that target lung ILC2s have rarely been reported. Here, we demonstrate that triptolide ameliorates allergic airway inflammation by suppressing ILC2 activation. IL-33, which is produced mainly by epithelial cells, is the most powerful cytokine for activating ILC2s. Triptolide-treated ILC2s were found to be functionally impaired in response to interleukin (IL)–33 challenge. RNA-seq analysis revealed that triptolide impaired ILC2 function through inflammation-related signalling pathways. ILC2-related genes were up- and down-regulated under the treatment with TPL such as Adrb2, Nmur1, tnfsf11, IL-5, IL-13, IL-9 and so on. Interestingly, we observed not only preventive but also therapeutic effects of triptolide on allergic airway inflammation, indicating that triptolide may serve as a promising traditional Chinese medicine for the treatment of allergic airway inflammation by targeting ILC2s.
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雷公藤甲素通过抑制2组先天淋巴样细胞功能减轻变应性气道炎症。
2组先天淋巴样细胞(ILC2s)产生2型细胞因子IL-5和IL-13,并参与2型免疫反应,如过敏性气道炎症。然而,针对肺部ILC2s的特异性药物,特别是中药,很少有报道。在这里,我们证明雷公藤甲素通过抑制ILC2激活来改善过敏性气道炎症。IL-33主要由上皮细胞产生,是激活ILC2s最有效的细胞因子。雷公藤甲素处理的ILC2s在响应白细胞介素(IL)-33攻击时功能受损。RNA-seq分析显示雷公藤甲素通过炎症相关信号通路损害ILC2功能。TPL处理下,ilc2相关基因Adrb2、Nmur1、tnfsf11、IL-5、IL-13、IL-9等均有上调和下调。有趣的是,我们观察到雷公藤甲素对变应性气道炎症不仅有预防作用,而且有治疗作用,这表明雷公藤甲素可能是一种很有希望通过靶向ILC2s治疗变应性气道炎症的中药。
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来源期刊
CiteScore
8.40
自引率
3.60%
发文量
935
审稿时长
53 days
期刊介绍: International Immunopharmacology is the primary vehicle for the publication of original research papers pertinent to the overlapping areas of immunology, pharmacology, cytokine biology, immunotherapy, immunopathology and immunotoxicology. Review articles that encompass these subjects are also welcome. The subject material appropriate for submission includes: • Clinical studies employing immunotherapy of any type including the use of: bacterial and chemical agents; thymic hormones, interferon, lymphokines, etc., in transplantation and diseases such as cancer, immunodeficiency, chronic infection and allergic, inflammatory or autoimmune disorders. • Studies on the mechanisms of action of these agents for specific parameters of immune competence as well as the overall clinical state. • Pre-clinical animal studies and in vitro studies on mechanisms of action with immunopotentiators, immunomodulators, immunoadjuvants and other pharmacological agents active on cells participating in immune or allergic responses. • Pharmacological compounds, microbial products and toxicological agents that affect the lymphoid system, and their mechanisms of action. • Agents that activate genes or modify transcription and translation within the immune response. • Substances activated, generated, or released through immunologic or related pathways that are pharmacologically active. • Production, function and regulation of cytokines and their receptors. • Classical pharmacological studies on the effects of chemokines and bioactive factors released during immunological reactions.
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