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Cigarette smoke inhibits BAFF expression and mucosal immunoglobulin A responses in the lung during influenza virus infection

机译:香烟烟雾抑制流感病毒感染期间肺中BAFF表达和黏膜免疫球蛋白A反应

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BackgroundIt is incompletely understood how cigarette smoke (CS) exposure affects lung mucosal immune responses during viral respiratory infections. B cell activating factor belonging to the tumor necrosis factor family (BAFF) plays an important role in the induction of secretory immunoglobulin A (S-IgA) which is the main effector of the mucosal immune system. We therefore investigated the effects of CS exposure on BAFF expression and S-IgA responses in the lung during influenza virus infection.MethodsMice were exposed to CS and/or infected with influenza virus. Bronchoalveolar lavage fluid and lung compartments were analyzed for BAFF expression, influenza-specific S-IgA level and histological changes. Lung B cells were isolated and the activation-induced cytidine deaminase (Aicda) expression was determined. BEAS-2B cells were treated with CS extract (CSE), influenza virus, interferon beta or N-acetylcysteine and BAFF expression was measured.ResultsCS inhibited BAFF expression in the lung, particularly after long-term exposure. BAFF and S-IgA levels were increased during influenza virus infection. Three-month CS exposure prior to influenza virus infection resulted in reduced BAFF and S-IgA levels in the lung as well as augmented pulmonary inflammation on day 7 after infection. Prior CS exposure also caused decreased Aicda expression in lung B cells during infection. Neutralization of BAFF in the lung resulted in reduced S-IgA levels during influenza virus infection. CSE inhibited virus-mediated BAFF induction in a dose-dependent manner in BEAS-2B cells, while this inhibition of BAFF by CSE was prevented by pretreatment with the antioxidant N-acetylcysteine.ConclusionsOur findings indicate that CS may hinder early mucosal IgA responses in the lung during influenza virus infection through oxidative inhibition of BAFF, which might contribute to the increased incidence and severity of viral infections in smokers.Electronic supplementary materialThe online version of this article (doi:10.1186/s12931-015-0201-y) contains supplementary material, which is available to authorized users.
机译:背景技术尚未完全了解香烟烟雾(CS)暴露如何影响病毒性呼吸道感染期间的肺粘膜免疫反应。属于肿瘤坏死因子家族(BAFF)的B细胞活化因子在分泌性免疫球蛋白A(S-IgA)的诱导中起重要作用,所述分泌性免疫球蛋白A是粘膜免疫系统的主要效应子。因此,我们调查了CS暴露对流感病毒感染期间肺中BAFF表达和S-IgA反应的影响。方法将小鼠暴露于CS和/或感染流感病毒。分析支气管肺泡灌洗液和肺室的BAFF表达,流感特异性S-IgA水平和组织学变化。分离肺B细胞,并测定活化诱导的胞苷脱氨酶(Aicda)表达。用CS提取物(CSE),流感病毒,干扰素β或N-乙酰半胱氨酸处理BEAS-2B细胞并测量BAFF表达。结果CS抑制了肺中的BAFF表达,特别是长期暴露后。在流感病毒感染期间,BAFF和S-IgA水平升高。流感病毒感染前三个月的CS暴露导致感染后第7天,肺中BAFF和S-IgA水平降低,肺部炎症加剧。先前的CS暴露也导致感染期间肺B细胞中Aicda表达下降。肺中BAFF的中和导致流感病毒感染期间S-IgA水平降低。 CSE在BEAS-2B细胞中以剂量依赖性方式抑制病毒介导的BAFF诱导,而用抗氧化剂N-乙酰半胱氨酸预处理可阻止CSE对BAFF的抑制。通过BAFF的氧化抑制在流感病毒感染过程中导致肺部感染,这可能导致吸烟者病毒感染的发生率和严重性增加。电子补充材料本文的在线版本(doi:10.1186 / s12931-015-0201-y)包含补充材料,可供授权用户使用。

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