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Attenuating immune pathology using a microbial-based intervention in a mouse model of cigarette smoke-induced lung inflammation

机译:在香烟烟雾诱发的肺部炎症小鼠模型中使用微生物干预减轻免疫病理

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摘要

BackgroundCigarette smoke exposure is the major risk factor for developing COPD. Presently, available COPD treatments focus on suppressing inflammation and providing bronchodilation. However, these options have varying efficacy in controlling symptoms and do not reverse or limit the progression of COPD. Treatments strategies using bacterial-derived products have shown promise in diseases characterized by inflammation and immune dysfunction. This study investigated for the first time whether a novel immunotherapy produced from inactivated Klebsiella (hereafter referred to as KB) containing all the major Klebsiella macromolecules, could attenuate cigarette smoke exposure-induced immune responses. We hypothesized that KB, by re-directing damaging immune responses, would attenuate cigarette smoke-induced lung inflammation and bronchoalveolar (BAL) cytokine and chemokine production.
机译:背景吸烟是发展COPD的主要危险因素。目前,可用的COPD治疗集中在抑制炎症和提供支气管扩张上。然而,这些选择在控制症状方面具有不同的功效,并且不会逆转或限制COPD的进展。使用细菌衍生产品的治疗策略在以炎症和免疫功能障碍为特征的疾病中显示出了希望。这项研究首次调查了由灭活的克雷伯菌(包含所有主要克雷伯菌)大分子产生的新型免疫疗法是否可以减弱卷烟烟雾暴露诱导的免疫反应。我们假设KB通过重新定向破坏性的免疫反应,可以减轻香烟烟雾引起的肺部炎症以及支气管肺泡(BAL)细胞因子和趋化因子的产生。

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