Interleukin-17A Expression Correlated with the Prognosis of Chronic Rhinosinusitis with Nasal Polyps and the Anti-Interleukin-17A Effect in a Murine Nasal Polyps Model

被引:5
|
作者
Huang, Jian-Cong [1 ]
Chen, Xiao-Hong [1 ]
Wang, Zhi-Yuan [1 ]
Li, Xia [1 ]
Chang, Li-Hong [1 ]
Zhang, Ge-Hua [1 ]
机构
[1] Sun Yat Sen Univ, Dept Otorhinolaryngol, Affiliated Hosp 3, 600 Tianhe Rd, Guangzhou 510080, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Interleukin-17A; Chronic rhinosinusitis with nasal polyps; Murine nasal polyps model; Matrix metalloproteinase-9; MATRIX METALLOPROTEINASES; INFLAMMATION; RECURRENCE; SUPERANTIGENS; EPIDEMIOLOGY; PATHOGENESIS; PROTEIN; IL-17;
D O I
10.1159/000507865
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective:To investigate the expression of interleukin-17A (IL-17A) in patients with chronic rhinosinusitis with nasal polyps (CRSwNP) and to analyze its effect on prognosis and to explore the role and mechanism of anti-IL-17A effect in vivo by establishing a murine nasal polyps (NP) model.Methods:Patients with CRSwNP who underwent endoscopic sinus surgery and matched control subjects were collected. We investigated IL-17A expression in human NP tissues using immunohistochemistry and analyzed their clinical features, including Lund-Mackay computed tomography scoring (LMCS) before surgery, Lund-Kennedy endoscopic scoring (LKES) before surgery (LKES B), LKES 6 months after surgery (LKES A), and reduction of LKES (LKES R). Then, after establishing the murine NP model to detect the expression and correlation of IL-17A and matrix metalloproteinase-9 (MMP-9) in nasal tissue, we studied nasal lavage fluid and serum by PCR and enzyme-linked immunosorbent assay in vivo. Anti-IL-17A treatment was administered in the murine NP model to confirm the function of IL-17A during the pathogenic processes.Results:IL-17A expression was upregulated in NP tissues from patients with CRSwNP compared with control subjects (p< 0.001). The number of IL-17A(+) cells was significantly negatively correlated with LKES R in patients with CRSwNP (p< 0.01). However, there was no significant correlation between IL-17A and LMCS or LKES B (allp< 0.05). Further, IL-17A and MMP-9 were more abundant in nasal mucosa of the murine NP model compared with that of control mice (allp< 0.05), and severe polypoid lesions were apparently observed in murine NP models. Anti-IL-17A treatment downregulated the mRNA and protein expression of MMP-9 in nasal mucosa and reduced the number of polypoid lesions in the murine NP model (allp< 0.05).Conclusion:Our results suggest that IL-17A plays a crucial role and may affect the prognosis of CRSwNP. Anti-IL-17A treatment may reduce the formation of polypoid lesions through inhibition of MMP-9 expression.
引用
收藏
页码:257 / 267
页数:11
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