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首页> 外文期刊>Cytokine >Effect of the fungal immunomodulatory protein FIP-fve on airway inflammation and cytokine production in mouse asthma model
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Effect of the fungal immunomodulatory protein FIP-fve on airway inflammation and cytokine production in mouse asthma model

机译:真菌免疫调节蛋白FIP-fve对小鼠哮喘模型气道炎症和细胞因子产生的影响

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摘要

The allergy is dependent on the balance between Th1 and Th2. The fungal immunodulatory protein (FIP-fve) was isolated from Flammulina velutipes. FIP-fve has been demonstrated to skew the response to Th1 cytokine production. We investigated whether oral administrations of FIP-fve inhibited allergen (OVA)-induced chronic airway inflammation in the mouse asthma model. After intranasal challenge with OVA, the airway inflammation and hyperresponsiveness were determined by bronchoalveolar lavage fluid (BALF) analysis and ELISA assay. Both pre-treated and post-treated with FIP-fve suppressed the airway hyperresponsiveness by methacholine challenge and significantly decreased the number of infiltrating inflammatory cells and Th2 cytokines in bronchoalveolar lavage fluid (BALF) and serum compared with the OVA sensitized mice. In addition, FIP-fve reduced OVA-specific IgE levels in serum. FIP-fve markedly alleviated the OVA-induced airway hyperresponsiveness (AHR) to inhaled methacholine. Based on lung histopathological studies using hematoxylin and Liu's staining, FIP-fve inhibited inflammatory cell infiltration compared with the OVA-sensitized mice. Oral FIP-fve had an anti-inflammatory effect on OVA-induced airway inflammations and might posses the potential for alternative therapy for allergic airway diseases.
机译:过敏取决于Th1和Th2之间的平衡。从金针菇分离出真菌免疫调节蛋白(FIP-fve)。已证明FIP-fve会使对Th1细胞因子产生的反应产生偏差。我们调查了FIP-fve的口服给药是否在小鼠哮喘模型中抑制了变应原(OVA)诱导的慢性气道炎症。用OVA鼻内攻击后,通过支气管肺泡灌洗液(BALF)分析和ELISA分析确定气道炎症和反应过度。与OVA致敏小鼠相比,FIP-fve预处理和后处理均通过甲酰胆碱攻击抑制了气道高反应性,并显着减少了支气管肺泡灌洗液(BALF)和血清中浸润性炎症细胞和Th2细胞因子的数量。另外,FIP-fve降低了血清中OVA特异性IgE水平。 FIP-fve显着减轻了OVA诱导的对吸入乙酰甲胆碱的气道高反应性(AHR)。根据使用苏木精和Liu染色的肺组织病理学研究,与OVA致敏小鼠相比,FIP-fve抑制了炎性细胞浸润。口服FIP-fve对OVA引起的气道炎症具有抗炎作用,并可能为过敏性气道疾病提供替代疗法的潜力。

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