Department of Immunology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Department of Geriatrics, Second Medical Center, PLA General Hospital, Beijing, China.
Cell Immunol. 2022 Jun;376:104536. doi: 10.1016/j.cellimm.2022.104536. Epub 2022 May 14.
Respiratory tract infection early in life plays a significant role in the pathogenesis of asthma. In the present study we examine, using a murine surrogate, the effects of early life respiratory infection with Streptococcus pneumoniae (SP) on adult asthma induced by sensitisation and exposure to house dust mite (HDM) allergen. Mice (one week old) were infected with SP, then 3 weeks later sensitised to HDM emulsified with Al (OH)3 intraperitoneally and challenged intranasally with same allergen for up to a further 5 weeks to establish the asthma surrogate. Outcome measures were quantified using the FlexiVent apparatus, histology and immunohistology, ELISA and flow cytometry. The murine surrogates of asthma infected with SP early in life exhibited significantly more severe disease compared with the controls of mice without SP infection, as shown by airways responsiveness, inflammatory cellular infiltration of the airways, expression of markers of airways remodelling, serum concentrations of HDM-specific IgE and the concentrations of Th2-type cytokines and the numbers of activated Th2 and ILC2 cells in the lung tissues. These data are compatible with the hypothesis that early-life infection of the airways with SP exacerbates, at least in some individuals, subsequent HDM-induced allergic airways inflammation and associated asthma in adulthood in this murine surrogate.
生命早期的呼吸道感染在哮喘发病机制中起着重要作用。本研究通过一种小鼠替代模型,研究了生命早期呼吸道感染肺炎链球菌(SP)对尘螨(HDM)过敏原致敏和暴露引起的成年哮喘的影响。小鼠(1 周龄)用 SP 感染,然后 3 周后用 Al(OH)3 乳化的 HDM 进行腹膜内致敏,并进行多达 5 周的相同过敏原的鼻腔内攻击,以建立哮喘替代模型。使用 FlexiVent 仪器、组织学和免疫组织化学、ELISA 和流式细胞术来定量评估结果。与未感染 SP 的对照组相比,早期感染 SP 的哮喘小鼠的哮喘替代模型表现出明显更严重的疾病,表现在气道反应性、气道炎症细胞浸润、气道重塑标志物的表达、血清 HDM 特异性 IgE 浓度以及肺组织中 Th2 型细胞因子的浓度和活化 Th2 和 ILC2 细胞的数量。这些数据与以下假设一致,即生命早期 SP 对气道的感染至少在某些个体中加重了随后的 HDM 诱导的过敏性气道炎症和成年期相关哮喘。