人类脂多糖挑战作为慢性阻塞性肺疾病恶化的模型。

Sergei A Kharitonov, Ulf Sjöbring
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引用次数: 49

摘要

内毒素,或脂多糖(LPS),是革兰氏阴性菌外细胞膜的组成部分。脂多糖是一种强效的促炎物质,当吸入时,剂量依赖性地引起发烧、发冷和支气管收缩。这些症状伴随着痰液和支气管肺泡灌洗液的促炎反应,中性粒细胞、巨噬细胞和某些细胞因子/趋化因子升高。这种反应可以用某些药物部分改变。在慢性阻塞性肺疾病(COPD)的稳定状态和这种疾病的恶化期间,都观察到类似的炎症变化。香烟烟雾中含有生物活性脂多糖,是慢性阻塞性肺病最常见的原因,也可能导致病情恶化。此外,下气道中存在革兰氏阴性菌是稳定期和加重期COPD的显著特征。基于这些知识,我们认为健康志愿者的吸入LPS刺激可以作为慢性阻塞性肺病的模型,也可以作为慢性阻塞性肺病恶化的模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lipopolysaccharide challenge of humans as a model for chronic obstructive lung disease exacerbations.

Endotoxin, or lipopolysaccharide (LPS), is a constituent of the outer cell membrane of Gram-negative bacteria. LPS is a highly potent proinflammatory substance, that, when inhaled, dose-dependently causes fever, chills, and bronchoconstriction. These symptoms are accompanied by a proinflammatory response in sputum and bronchoalveolar lavage fluid with elevation of neutrophils, macrophages and certain cytokines/chemokines. This response can be partially modified with certain drugs. Similar inflammatory changes are observed both in the stable state of chronic obstructive lung disease (COPD) and during exacerbations of this disease. Cigarette smoke, which contains bioactive LPS, is the most common cause of COPD and may also precipitate exacerbations. In addition, the presence of Gram-negative bacteria in the lower airways is a distinguishing feature both of stable COPD and of exacerbations. Based on this knowledge we argue here that inhaled LPS provocation of healthy volunteers can be used as a model or COPD as well as for exacerbations of this disease.

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