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Immunization with live influenza viruses in an experimental model of allergic bronchial asthma: infection and vaccination

机译:过敏性支气管哮喘实验模型中的活流感病毒免疫:感染和疫苗接种

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Background Asthmatics in particular have a need for influenza vaccines because influenza infection is a frequent cause of hospitalization of patients with bronchial asthma. Currently, only inactivated influenza vaccines are recommended for influenza prevention in asthma sufferers. Objective The aim of our study was to analyze and compare the effects of influenza infection and vaccination with live attenuated influenza vaccine (LAIV) on different phases of experimental murine allergic bronchial asthma (acute asthma and remission phase) and on subsequent exposure to allergen in sensitized animals. Methods Ovalbumin (OVA)-specific serum IgE levels, IL-4 production by spleen and lung lymphocytes, and histological changes in the lungs of mice infected with pathogenic virus or LAIV were studied at two phases of OVA-induced bronchial asthma (acute asthma and remission). Results Infection with pathogenic virus both in acute asthma and remission led to asthma exacerbation associated with the production of OVA-specific IgE, IL-4 and significant inflammatory infiltration in airways. Infection, even after complete virus clearance, induced the aggravation of lung inflammation and IgE production in asthmatic mice additionally exposed to OVA. Immunization with LAIV at remission did not enhance allergic inflammatory changes in the lung, OVA-specific IgE or IL-4 production. Then after additional OVA exposure, histological and immunological changes in these mice were the same as in the control group. Conclusions Influenza infection provokes asthma exacerbation regardless of the disease phase. Immunization with LAIV during the remission phase of bronchial asthma is safe and does not interfere upon subsequent contact of asthma sufferers with allergen.
机译:背景技术哮喘患者尤其需要哮喘疫苗,因为流感感染是支气管哮喘患者住院的常见原因。当前,仅推荐灭活的流感疫苗用于哮喘患者的流感预防。目的本研究的目的是分析和比较流感病毒减毒活疫苗的接种和疫苗接种对实验性鼠过敏性支气管哮喘不同阶段(急性哮喘和缓解期)以及随后致敏的过敏原暴露的影响。动物。方法研究卵白蛋白(OVA)特异性血清IgE水平,脾脏和肺淋巴细胞IL-4的产生以及感染致病性病毒或LAIV的小鼠肺组织学变化的两个阶段,分别由OVA诱发的支气管哮喘(急性哮喘和缓解)。结果在急性哮喘和缓解期均感染致病病毒会导致哮喘加重,并伴有OVA特异性IgE,IL-4的产生以及气道中明显的炎症浸润。即使在完全清除病毒后,感染也会使另外暴露于OVA的哮喘小鼠的肺部炎症和IgE产生加剧。缓解时用LAIV免疫并未增强肺部过敏性炎症变化,OVA特异性IgE或IL-4产生。然后在额外的OVA暴露后,这些小鼠的组织学和免疫学变化与对照组相同。结论流感感染不论病发阶段如何,均会加剧哮喘发作。在支气管哮喘缓解期使用LAIV免疫是安全的,并且不会干扰哮喘患者随后与过敏原的接触。

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