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Inactivated influenza virus vaccine is efficient and reduces IL‐4 and IL‐6 in allergic asthma mice

机译:灭活流感病毒疫苗有效,可降低过敏性哮喘小鼠的IL-4和IL-6

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AbstractBackgroundAllergic asthma is a globally respiratory inflammatory disease. Influenza virus is a respiratory pathogen that causes yearly epidemics and results in high rates of morbidity and mortality. Patients with allergic asthma had a more severe symptom and a higher mortality when they were infected with influenza virus. Hence, influenza vaccination is recommended for patients with asthma.ObjectivesWe evaluated the efficacy and effects of influenza vaccination on allergic asthma in a mouse model.MethodsOvalbumin-immunized mice were inoculated with inactivated influenza virus A/Puerto Rico/8/34 (PR8) as vaccines and morbidity or mortality and allergic asthma features of these mice were analyzed.ResultsMice inoculated with inactivated PR8 induced high levels of anti-PR8 IgG2a and upregulation of Toll-like receptor (TLR) 7. Vaccinated allergic mice were healthy when they were challenged with live influenza virus while none of non-vaccinated allergic mice survived. Furthermore, inactivated influenza virus vaccine induced neither extra airway inflammation nor asthma features such as IgE, airway hyper-reactivity, and eosinophilia in allergic mice. Particularly, decreased frequency of immune cell infiltrated airways and Th2 cytokines IL-4 and IL-6 production in the bronchoalveolar lavage fluid were noted in vaccinated allergic mice. These results suggested that inactivated influenza virus vaccine is efficient to protect allergic mice from further influenza infection, and it does not exacerbate but reduces IL-4 and IL-6 of allergic asthma.ConclusionInfluenza vaccination is essential and efficient for allergic subjects to protect influenza virus infection.
机译:摘要背景过敏性哮喘是一种全球性呼吸道炎性疾病。流感病毒是一种呼吸道病原体,每年引起流行病,并导致高发病率和死亡率。过敏性哮喘患者感染流感病毒后,症状更严重,死亡率更高。因此,建议对哮喘患者进行流感疫苗接种。结果对接种灭活PR8的小鼠诱导了高水平的抗PR8 IgG2a以及Toll样受体(TLR)的上调。7接种疫苗的变态小鼠在受到挑战后是健康的。活流感病毒,而未接种疫苗的过敏小鼠均未存活。此外,灭活的流感病毒疫苗在变应性小鼠中既不引起额外的气道炎症也不引起哮喘特征,例如IgE,气道高反应性和嗜酸性粒细胞增多。尤其是,在接种疫苗的过敏性小鼠中,免疫细胞浸润气道的频率降低,支气管肺泡灌洗液中Th2细胞因子IL-4和IL-6的产生减少。这些结果表明灭活的流感病毒疫苗可以有效保护变态反应小鼠免受进一步的流感病毒感染,并且不会加剧变应性哮喘的IL-4和IL-6降低。结论流感疫苗对于变应性受试者保护流感病毒是必不可少且有效的感染。

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