Xiao-qing-long-tang ameliorates OVA-induced allergic rhinitis by inhibiting ILC2s through the IL-33/ST2 and JAK/STAT pathways

被引:6
作者
Zhang, Jia-jun [1 ,3 ]
He, Xue-cheng [1 ]
Zhou, Min [2 ]
Liu, Qin-dong [1 ]
Xu, Wei-zhen [1 ]
Yan, Ya-jie [2 ,4 ,5 ]
Ruan, Yan [2 ,4 ,5 ]
机构
[1] Guangzhou Univ Chinese Med, Clin Med Coll 1, Guangzhou 510405, Peoples R China
[2] Guangzhou Univ Chinese Med, Affiliated Hosp 1, Otorhinolaryngol Dept, Guangzhou 510405, Peoples R China
[3] Southern Med Univ, Affiliated Foshan Hosp, Peoples Hosp Foshan 2, Dept Pathol, Foshan 528099, Guangdong Provi, Peoples R China
[4] Guangdong Clin Res Acad Chinese Med, Guangzhou 510405, Peoples R China
[5] Guangzhou Univ Chinese Med, Otorhinolaryngol Dept, Affiliated Hosp 1, 16 Jichang Rd, Guangzhou 510405, Guangdong Provi, Peoples R China
基金
中国国家自然科学基金;
关键词
Xiao-qing-long-tang; Allergic rhinitis; ILC2s; IL-33/ST2; signaling; JAK/STAT pathway; INNATE LYMPHOID-CELLS;
D O I
10.1016/j.phymed.2023.155012
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Allergic rhinitis (AR) is a chronic inflammatory disease of the nasal mucosa that is mediated by immunoglobulin E (IgE). Xiao-qing-long-tang (XQLT) is a traditional Chinese medicine compound that is widely used to treat respiratory diseases such as AR. However, the underlying mechanism of the effect of XQLT on AR remains unclear. Purpose: To elucidate the effect of XQLT on ovalbumin (OVA)-induced AR and the mechanisms of action. Methods: The therapeutic efficacy of XQLT was evaluated in a well-established OVA-induced AR mouse model. Nasal symptoms were analyzed, type 2 cytokines and OVA-sIgE levels were measured, nasal mucosa tissues were collected for histological analysis, and the changes of Group 2 innate lymphoid cells (ILC2s) and the IL-33/ST2 and JAK/STAT signaling pathways in the nasal mucosa were observed. Results: XQLT significantly alleviated the nasal symptoms and histological damage to the nasal mucosa in AR mice, and reduced the levels of type 2 cytokines and OVA-sIgE. In addition, after XQLT treatment, the numbers of ILC2s in the nasal mucosa of AR mice were reduced, and the mRNA levels of the transcription factors GATA3 and ROR-alpha were decreased. Moreover, IL-33/ST2 signaling pathway was inhibited. The costimulatory cytokine associated JAK/STAT signaling pathway was also inhibited in ILC2s. Conclusion: Our study demonstrated that XQLT regulated ILC2s through the IL-33/ST2 and JAK/STAT pathways to ameliorate type 2 inflammation in OVA-induced AR. These findings suggest that XQLT might be used to treat AR.
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页数:12
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