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经气管内接种肺炎链球菌诱导的中风后肺炎小鼠模型

A Mouse Model of Post-Stroke Pneumonia Induced by Intra-Tracheal Inoculation with Streptococcus pneumoniae.

作者信息

Mracsko Eva, Stegemann-Koniszewski Sabine, Na Shin-Young, Dalpke Alexander, Bruder Dunja, Lasitschka Felix, Veltkamp Roland

机构信息

Department of Neurology, University Heidelberg, Heidelberg, Germany.

出版信息

Cerebrovasc Dis. 2017;43(3-4):99-109. doi: 10.1159/000452136. Epub 2017 Jan 4.

Abstract

BACKGROUND

Stroke-induced immunodeficiency increases the risk of infectious complications, which adversely affects neurological outcome. Among those, pneumonia affects as many as one third of stroke patients and is the main contributor to mortality in the post-acute phase of stroke. Experimental findings on post-stroke susceptibility to spontaneous pneumonia in mice are contradictory. Here, we established a mouse model inducing standardized bacterial pneumonia and characterized the impaired pulmonary cellular and humoral immune responses after experimental stroke.

METHODS

Bacterial pneumonia was induced by intra-tracheal inoculation with Streptococcus pneumoniae at different time points after transient middle cerebral artery occlusion (MCAO). Bacterial counts in lungs and blood, histological changes, and cytokine production in the lungs were assessed. Furthermore, we investigated the effect of pneumonia on stroke outcome.

RESULTS

Intra-tracheal inoculation resulted in reproducible pneumonia and bacteraemia, and demonstrated post-stroke susceptibility to streptococcal pneumonia developing with a delay of at least 24 h after MCAO. Higher bacterial counts in mice infected 3 days after stroke induction correlated with reduced neutrophil and macrophage infiltration in the lungs and lower levels of pro-inflammatory cytokines in the broncho-alveolar lavage compared to sham-operated animals. Pneumonia increased mortality without affecting brain-infiltrating leukocytes.

CONCLUSIONS

In this standardized mouse model of post-stroke pneumonia, we describe attenuated leukocyte infiltration and cytokine production in response to bacterial infection in the lungs that has a profound effect on outcome.

摘要

背景

中风诱发的免疫缺陷会增加感染性并发症的风险,对神经功能结局产生不利影响。其中,肺炎影响多达三分之一的中风患者,是中风急性期后死亡的主要原因。关于小鼠中风后对自发性肺炎易感性的实验结果相互矛盾。在此,我们建立了一种诱导标准化细菌性肺炎的小鼠模型,并对实验性中风后受损的肺细胞免疫和体液免疫反应进行了表征。

方法

在短暂性大脑中动脉闭塞(MCAO)后的不同时间点,通过气管内接种肺炎链球菌诱导细菌性肺炎。评估肺和血液中的细菌计数、组织学变化以及肺中的细胞因子产生。此外,我们研究了肺炎对中风结局的影响。

结果

气管内接种导致可重复性肺炎和菌血症,并证明中风后对链球菌性肺炎易感,在MCAO后至少延迟24小时出现。与假手术动物相比,中风诱导后3天感染的小鼠中较高的细菌计数与肺中中性粒细胞和巨噬细胞浸润减少以及支气管肺泡灌洗中促炎细胞因子水平降低相关。肺炎增加了死亡率,但不影响脑内浸润白细胞。

结论

在这个标准化的中风后肺炎小鼠模型中,我们描述了肺部对细菌感染的白细胞浸润和细胞因子产生减弱,这对结局有深远影响。

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