过敏原诱导过敏性哮喘患者血液 Th2 和 Th17 细胞中 IL-18 和 IL-18Rα 表达上调

Junling Wang, Mengmeng Zhan, Yaping Zhai, Siqin Wang, Fangqiu Gu, Zhuo Zhao, Zhaolong Zhang, Yifei Li, Xin Dong, Yijie Zhang, Bingyu Qin
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摘要

过敏性哮喘(AA)与T辅助细胞(Th)2和Th17细胞的极化密切相关。白细胞介素(IL)-18 是 Th2 和 Th17 细胞反应的诱导因子。然而,IL-18和IL-18受体α(IL-18Rα)在AA患者血液Th2和Th17细胞中的表达仍不清楚。因此,我们利用流式细胞分析、定量实时 PCR(qPCR)和小鼠 AA 模型研究了它们在 Th2 和 Th17 细胞中的表达。我们在 AA 患者的血液 CD4+ T 细胞中观察到 Th2、Th17、IL-18+、IL-18+ Th2 和 IL-18+ Th17 细胞的比例增加。此外,屋尘螨似乎还能进一步上调 Th2 和 Th17 细胞中 IL-18 的表达,并上调 AA 患者 CD4+ T、Th2 和 Th17 细胞中 IL-18Rα 的表达。研究还发现,AA 患者血浆中的 IL-4、IL-17A 和 IL-18 水平升高,且三者之间存在相关性。在卵清蛋白(OVA)诱导的哮喘小鼠(AM)中,我们观察到血液中 CD4+ T、Th2 和 Th17 细胞的百分比增加。此外,OVA诱导的哮喘小鼠血液Th2细胞中IL-18Rα表达水平较高,而IL-18可对其进行下调。在 OVA 诱导的 FcεRIα-/- 小鼠血液 Th2 细胞中也观察到 IL-18Rα 表达增加。总之,我们的研究结果表明,Th2细胞在对过敏原做出反应时表达过量的IL-18和IL-18Rα,从而参与了AA,表达IL-18和IL-18Rα的Th2细胞可能是AA治疗的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Allergens induce upregulated IL-18 and IL-18Rα expression in blood Th2 and Th17 cells of patients with allergic asthma
Allergic asthma (AA) is closely associated with the polarization of T helper (Th)2 and Th17 cells. Interleukin (IL)-18 acts as an inducer of Th2 and Th17 cell responses. However, expressions of IL-18 and IL-18 receptor alpha (IL-18Rα) in blood Th2 and Th17 cells of patients with AA remain unclear. We therefore investigated their expressions in Th2 and Th17 cells using flow cytometric analysis, quantitative real-time PCR (qPCR), and murine AA model. We observed increased proportions of Th2, Th17, IL-18+, IL-18+ Th2, and IL-18+ Th17 cells in blood CD4+ T cells of patients with AA. Additionally, house dust mite seemed to upregulate further IL-18 expression in Th2 and Th17, and upregulate IL-18Rα expression in CD4+ T, Th2, and Th17 cells of AA patients. It was also found that the plasma levels of IL-4, IL-17A, and IL-18 in AA patients were elevated, and they were correlated between each other. In ovalbumin (OVA)-induced asthma mouse (AM), we observed that the percentages of blood CD4+ T, Th2, and Th17 cells were increased. Moreover, OVA-induced AM expressed higher level of IL-18Rα in blood Th2 cells, which was downregulated by IL-18. Increased IL-18Rα expression was also observed in blood Th2 cells of OVA-induced FcεRIα−/− mice. Collectively, our findings suggest the involvement of Th2 cells in AA by expressing excessive IL-18 and IL-18Rα in response to allergen, and that IL-18 and IL-18Rα expressing Th2 cells are likely to be the potential targets for AA therapy.
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