嗜酸性粒细胞在哮喘和呼吸道病毒感染中的抗病毒作用。

IF 3.3 Q2 ALLERGY
Frontiers in allergy Pub Date : 2025-02-28 eCollection Date: 2025-01-01 DOI:10.3389/falgy.2025.1548338
Hisashi Sasaki, Jun Miyata, Akihiko Kawana, Koichi Fukunaga
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引用次数: 0

摘要

嗜酸性粒细胞是一种免疫细胞,对过敏性疾病(如哮喘)的发病机制至关重要。这些细胞在包括感染在内的各种情况下发挥着多功能作用。它们在病毒感染时被激活并发挥抗病毒活性。模式识别受体,toll样受体7和视黄酸诱导基因i对RNA病毒的识别和捕获至关重要。此外,细胞内颗粒蛋白(嗜酸性粒细胞阳离子蛋白和嗜酸性粒细胞衍生的神经毒素)和细胞内一氧化氮的产生灭活和/或降解RNA病毒。有趣的是,嗜酸性粒细胞合成的特殊促分解介质具有抑制病毒复制的抗病毒特性。因此,嗜酸性粒细胞可能在呼吸道病毒感染中起保护作用。值得注意的是,哮喘患者的抗病毒活性受损,嗜酸性粒细胞活性的紊乱与哮喘的严重程度成正比。嗜酸性粒细胞在RNA病毒(鼻病毒、呼吸道合胞病毒和流感病毒)诱导的2型炎症性哮喘加重中的确切作用尚不清楚。我们的研究表明干扰素(IFN-α和IFN-γ)刺激人类嗜酸性粒细胞上调抗病毒分子,包括鸟苷酸结合蛋白和三方基序。此外,IFN-γ特异性地增加IL5RA、ICAM-1和FCGR1A的表达,可能分别增强细胞对IL-5、ICAM-1介导的鼻病毒粘附和igg诱导的炎症反应的反应性。本文综述了病毒感染与哮喘之间的关系,以及人和小鼠嗜酸性粒细胞体内和体外抗病毒功能发展的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antiviral roles of eosinophils in asthma and respiratory viral infection.

Eosinophils are immune cells that are crucial for the pathogenesis of allergic diseases, such as asthma. These cells play multifunctional roles in various situations, including infection. They are activated during viral infections and exert antiviral activity. Pattern recognition receptors, toll-like receptor 7 and retinoic acid inducible gene-I, are important for the recognition and capture of RNA viruses. In addition, intracellular granule proteins (eosinophil cationic protein and eosinophil-derived neurotoxin) and intracellular nitric oxide production inactivate and/or degrade RNA viruses. Interestingly, eosinophil-synthesizing specialized pro-resolving mediators possess antiviral properties that inhibit viral replication. Thus, eosinophils may play a protective role during respiratory virus infections. Notably, antiviral activities are impaired in patients with asthma, and eosinophil activities are perturbed in proportion with the severity of asthma. The exact roles of eosinophils in RNA virus (rhinovirus, respiratory syncytial virus, and influenza virus)-induced type 2 inflammation-based asthma exacerbation remain unclear. Our research demonstrates that interferons (IFN-α and IFN-γ) stimulate human eosinophils to upregulate antiviral molecules, including guanylate-binding proteins and tripartite motifs. Furthermore, IFN-γ specifically increases the expression of IL5RA, ICAM-1, and FCGR1A, potentially enhancing cellular responsiveness to IL-5, ICAM-1-mediated adhesion to rhinoviruses, and IgG-induced inflammatory responses, respectively. In this review, we have summarized the relationship between viral infections and asthma and the mechanisms underlying the development of antiviral functions of human and mouse eosinophils in vivo and in vitro.

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CiteScore
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