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辅助性 T 细胞 9 激活参与变应性鼻炎的小鼠模型。

Involvement of T-Helper 9 Activation in a Mouse Model of Allergic Rhinitis.

机构信息

Department of Otorhinolaryngology Head and Neck Surgery, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China (mainland).

Department of Otorhinolaryngology Head and Neck Surgery, The Third Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China (mainland).

出版信息

Med Sci Monit. 2018 Jul 8;24:4704-4710. doi: 10.12659/MSM.908302.

Abstract

BACKGROUND We aimed to investigate the role of T-Helper (TH) 9 cells in the pathogenesis of allergic rhinitis (AR) in mice. MATERIAL AND METHODS An AR model was produced in BALB/c mice, and the viral encoding interleukin (IL)-9 silencing sequence was used to reduce IL-9 expression. The experiment was divided into a control group, an AR group, an IL-9 shRNA+AR group, and a vector+AR group. Hematoxylin and eosin (H&E) staining was used to detect pathological changes. The cytokine expression was detected by ELISA method. Cellular typing was detected by flow cytometry. RESULTS Cells in the control group were regularly arranged, with clear layers and no congestion, edema, or necrosis observable. By contrast, in the AR model group and the vector treatment group, nasal mucosa showed clear hyperemia and edema in upper tissues and infiltration of inflammatory cells, which were ameliorated by IL-9 silencing. Compared with the control group, interferon-γ (IFN-γ) was significantly down-regulated, while IL-4, IL-17, and IL-9 were significantly elevated in the AR model group. TH1 cells in nasal mucosa, lymph, nasal lavage, spleen, and peripheral blood were significantly reduced, while TH2, TH9, TH17, and Treg cells were significantly elevated in the AR group compared with the control group. Importantly, all these changes in AR model were ameliorated by IL-9 silencing. CONCLUSIONS AR is related to the changes of cytokines in TH1, TH2, TH9, TH17, and Treg, which are improved by IL-9 silencing. Activation of TH9 cells is involved in the pathogenesis of AR.

摘要

背景

本研究旨在探讨辅助性 T 细胞(TH)9 细胞在变应性鼻炎(AR)发病机制中的作用。

材料和方法

采用 BALB/c 小鼠建立 AR 模型,应用病毒编码的白细胞介素(IL)-9 沉默序列降低 IL-9 的表达。实验分为对照组、AR 组、IL-9 shRNA+AR 组和载体+AR 组。采用苏木精和伊红(H&E)染色观察病理变化,酶联免疫吸附试验(ELISA)检测细胞因子表达,流式细胞术检测细胞分型。

结果

对照组细胞排列规则,层次清晰,未见充血、水肿和坏死。相比之下,在 AR 模型组和载体治疗组,鼻黏膜上组织明显出现充血和水肿,以及炎性细胞浸润,而这些改变在 IL-9 沉默后得到改善。与对照组相比,AR 模型组中干扰素-γ(IFN-γ)明显下调,而 IL-4、IL-17 和 IL-9 明显升高。与对照组相比,鼻黏膜、淋巴结、鼻腔灌洗液、脾脏和外周血中的 TH1 细胞明显减少,而 TH2、TH9、TH17 和 Treg 细胞明显增加。重要的是,IL-9 沉默可改善 AR 模型中的所有这些变化。

结论

AR 与 TH1、TH2、TH9、TH17 和 Treg 细胞中细胞因子的变化有关,而 IL-9 沉默可改善这些变化。TH9 细胞的激活参与了 AR 的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7af/6069443/49bbf7f1b013/medscimonit-24-4704-g001.jpg

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