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Oral administration of Lactobacillus paracasei L9 attenuates PM2.5-induced enhancement of airway hyperresponsiveness and allergic airway response in murine model of asthma

机译:口服副干酪乳杆菌L9可减轻PM2.5诱导的哮喘小鼠模型中气道高反应性和过敏性气道反应的增强

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摘要

This study investigated allergy immunotherapy potential of Lactobacillus paracasei L9 to prevent or mitigate the particulate matter 2.5 (PM2.5) enhanced pre-existing asthma in mice. Firstly, we used a mouse model of asthma (a 21-day ovalbumin (OVA) sensitization and challenge model) followed by PM2.5 exposure twice on the same day of the last challenge. PM2.5 was collected from the urban area of Beijing and underwent analysis for metals and polycyclic aromatic hydrocarbon contents. The results showed that PM2.5 exposure enhanced airway hyper-responsiveness (AHR) and lead to a mixed Th2/ IL-17 response in asthmatic mice. Secondly, the PM2.5 exposed asthmatic mice were orally administered with L9 (4×107, 4×109 CFU/mouse, day) from the day of first sensitization to the endpoint, for 20 days, to investigate the potential mitigative effect of L9 on asthma. The results showed that L9 ameliorated PM2.5 exposure enhanced AHR with an approximate 50% decrease in total airway resistance response to methacholine (48 mg/ml). L9 also prevented the exacerbated eosinophil and neutrophil infiltration in bronchoalveolar lavage fluid (BALF), and decreased the serum level of total IgE and OVA-specific IgG1 by 0.44-fold and 0.3-fold, respectively. Additionally, cytokine production showed that L9 significantly decreased T-helper cell type 2 (Th2)–related cytokines (IL-4, -5, -13) and elevated levels of Th1 related IFN-γ in BALF. L9 also reduced the level of IL-17A and increased the level of TGF-β. Taken together, these results indicate that L9 may exert the anti-allergic benefit, possibly through rebalancing Th1/Th2 immune response and modulating IL-17 pro-inflammatory immune response. Thus, L9 is a promising candidate for preventing PM exposure enhanced pre-existing asthma.
机译:这项研究调查了Lasetobacillus paracasei L9预防或减轻小鼠体内微粒物质2.5(PM2.5)增强的已有哮喘的变态反应免疫治疗的潜力。首先,我们使用了哮喘小鼠模型(21天卵清蛋白(OVA)致敏和激发模型),然后在最后一次激发的同一天两次暴露于PM2.5。 PM2.5采集自北京市区,并进行了金属和多环芳烃含量的分析。结果显示,PM2.5暴露增强哮喘小鼠的气道高反应性(AHR),并导致混合的Th2 / IL-17反应。其次,从首次致敏之日起,对暴露于PM2.5的哮喘小鼠口服L9(每天4×10 7 ,4×10 9 CFU /小鼠)。到终点,持续20天,以研究L9对哮喘的潜在缓解作用。结果表明,L9改善了PM2.5暴露水平,从而提高了AHR,对乙酰甲胆碱(48 mg / ml)的总气道阻力响应降低了约50%。 L9还阻止了支气管肺泡灌洗液(BALF)中嗜酸性粒细胞和中性粒细胞浸润的加剧,并使总IgE和OVA特异性IgG1的血清水平分别降低了0.44倍和0.3倍。此外,细胞因子的产生表明L9显着降低了BALF中2型T辅助细胞(Th2)相关的细胞因子(IL-4,-5,-13)和Th1相关IFN-γ的水平。 L9还降低了IL-17A的水平,并提高了TGF-β的水平。综上所述,这些结果表明L9可能通过平衡Th1 / Th2免疫应答和调节IL-17促炎性免疫应答发挥抗过敏作用。因此,L9是预防PM暴露增强的既存哮喘的有希望的候选者。

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