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鼠李糖乳杆菌抑制 Th17 促炎反应并减轻变应原诱导的过敏性哮喘小鼠模型中的气道炎症。

Lactobacillus gasseri suppresses Th17 pro-inflammatory response and attenuates allergen-induced airway inflammation in a mouse model of allergic asthma.

机构信息

Department of Pediatrics, Chi-Mei Medical Center, Liou-Yin, Tainan, Taiwan, ROC.

出版信息

Br J Nutr. 2012 Jul 14;108(1):130-9. doi: 10.1017/S0007114511005265.

DOI:10.1017/S0007114511005265
PMID:21996276
Abstract

Probiotics are normal inhabitants of the gastrointestinal tract of man and are widely considered to exert a number of beneficial effects in many diseases. But the mechanism by which they modulate the immune system is poorly understood. The present study was planned to explore the anti-allergic effect of Lactobacillus gasseri on a mouse model of allergic asthma. Dermatophoides pteronyssinus (Der p) sensitised and challenged BALB/c mice were orally administered via oral administration with three different doses of L. gasseri (low, 1 × 10(6) colony-forming units (CFU); medium, 2 × 10(6) CFU; high, 4 × 10(6) CFU), in 700 μl of PBS daily, starting from 2 weeks before Der p sensitisation for 4 weeks. After the allergen challenge, airway responsiveness to methacholine, influx of inflammatory cells to the lung, and cytokine levels in bronchoalveolar lavage (BAL) fluids and splenocytes culture were assessed. Our results showed that oral administration of a high dose of L. gasseri (4 × 10(6) CFU) decreased airway responsiveness to methacholine, attenuated the influx of inflammatory cells to the airways and reduced the levels of TNF-α, thymus and activation-regulated chemokine (TARC) and IL-17A in BAL fluids of Der p-sensitised and -challenged mice. Moreover, L. gasseri decreased IL-17A production in transforming growth factor-α and IL-6 stimulated splenocytes and cell numbers of IL-17 producing alveolar macrophages in L. gasseri-treated mice as compared to non-treated, Der p-sensitised and -challenged mice. In conclusion, oral administration with L. gasseri can attenuate major characteristics of allergen-induced airway inflammation and IL-17 pro-inflammatory immune response in a mouse model of allergic asthma, which may have clinical implication in the preventive or therapeutic potential in allergic asthma.

摘要

益生菌是人类胃肠道的正常居民,被广泛认为在许多疾病中发挥多种有益作用。但它们调节免疫系统的机制尚不清楚。本研究旨在探索干酪乳杆菌对变应性哮喘小鼠模型的抗过敏作用。用变应原皮氏肺孢子菌(Der p)致敏和攻击 BALB/c 小鼠,用三种不同剂量的干酪乳杆菌(低剂量 1×10^6 个菌落形成单位(CFU);中剂量 2×10^6 CFU;高剂量 4×10^6 CFU)通过口服灌胃,每日 700μl PBS,从 Der p 致敏前 2 周开始持续 4 周。在过敏原攻击后,评估气道对乙酰甲胆碱的反应性、炎症细胞向肺内的浸润以及支气管肺泡灌洗液(BAL)和脾细胞培养物中的细胞因子水平。我们的结果表明,高剂量干酪乳杆菌(4×10^6 CFU)口服给药可降低气道对乙酰甲胆碱的反应性,减弱炎症细胞向气道的浸润,并降低 Der p 致敏和攻击小鼠 BAL 液中 TNF-α、胸腺和激活调节趋化因子(TARC)和 IL-17A 的水平。此外,与未经处理、Der p 致敏和攻击的小鼠相比,干酪乳杆菌降低了转化生长因子-α和 IL-6 刺激的脾细胞中 IL-17A 的产生,以及干酪乳杆菌处理小鼠中 IL-17 产生的肺泡巨噬细胞的数量。总之,口服干酪乳杆菌可减轻变应原诱导的气道炎症和 IL-17 促炎免疫反应的主要特征,这可能对预防或治疗变应性哮喘具有临床意义。

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