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鼻腔内长双歧杆菌可预防致死性流感感染小鼠模型中病毒引起的肺部炎症和损伤。

Intranasal Bifidobacterium longum protects against viral-induced lung inflammation and injury in a murine model of lethal influenza infection.

机构信息

Alimentary Health Pharma Davos, Davos, Switzerland; PrecisionBiotics Group Ltd., Cork, Ireland; Lead contact.

Alimentary Health Pharma Davos, Davos, Switzerland; Swiss Institute of Allergy and Asthma Research (SIAF), University of Zurich, Davos, Switzerland.

出版信息

EBioMedicine. 2020 Oct;60:102981. doi: 10.1016/j.ebiom.2020.102981. Epub 2020 Sep 11.

Abstract

BACKGROUND

Prophylactic strategies are urgently needed for prevention of severe inflammatory responses to respiratory viral infections. Bacterial-host interactions may modify the immune response to viral infections.

METHODS

We examined the contribution of Intranasal administration of two different Bifidobacterium longum strains or its isolated cell wall in controlling viral induced inflammation using a murine model of influenza infection. We monitored mortality and morbidity over a 10-day period and viral load, differential broncho alveolar lavage (BAL) fluid inflammatory cell counts, Lung tissue histology, BAL and serum cytokines, markers of vascular damage and cell death were quantified.

FINDINGS

Intranasal administration of Bifidobacterium longum35624® or its isolated cell wall prior to virus inoculation significantly reduced viral load within the lungs and significantly improved survival. Reduced viral load was associated with reduced lung injury as suggested by cell death and vascular leakage markers, a shift from neutrophil to macrophage recruitment, reduced inflammatory cytokine levels (including IL-6), reduced type 1 and 2 interferon levels, but increased levels of interferon-λ and surfactant protein D. These protective effects were maintained when the bifidobacterial cell wall preparation was administered 24 h after viral inoculation. The protective effects were also observed for the Bifidobacterium longumPB-VIR™ strain.

INTERPRETATION

Exposure to these bifidobacterial strains protect against the inflammatory sequelae and damage associated with uncontrolled viral replication within the lung.

FUNDING

This work has been funded, in part, by a research grant from GlaxoSmithKline, PrecisionBiotics Group Ltd., Swiss National Science Foundation grants (project numbers CRSII3_154488, 310030_144219, 310030_127356 and 310030_144219) and Christine Kühne - Center for Allergy Research and Education (CK-CARE).

摘要

背景

迫切需要预防策略来预防呼吸道病毒感染引起的严重炎症反应。细菌-宿主相互作用可能会改变对病毒感染的免疫反应。

方法

我们使用流感感染的小鼠模型,研究了两种不同长双歧杆菌菌株或其分离的细胞壁经鼻腔给药在控制病毒诱导的炎症中的作用。我们在 10 天的时间内监测死亡率和发病率以及病毒载量、差异支气管肺泡灌洗液 (BAL) 炎症细胞计数、肺组织学、BAL 和血清细胞因子、血管损伤和细胞死亡标志物。

发现

在病毒接种前鼻内给予长双歧杆菌 35624®或其分离的细胞壁可显著降低肺部的病毒载量,并显著提高存活率。病毒载量的降低与肺损伤的减少有关,这表现在细胞死亡和血管渗漏标志物、从中性粒细胞向巨噬细胞募集的转变、炎症细胞因子水平(包括 IL-6)、1 型和 2 型干扰素水平的降低以及干扰素-λ和表面活性剂蛋白 D 水平的增加。当双歧杆菌细胞壁制剂在病毒接种后 24 小时给予时,这些保护作用得以维持。长双歧杆菌 PB-VIR™菌株也观察到了这种保护作用。

解释

接触这些双歧杆菌菌株可预防与肺部不受控制的病毒复制相关的炎症后遗症和损伤。

资金

这项工作得到了葛兰素史克公司部分研究资助、PrecisionBiotics Group Ltd. 资助、瑞士国家科学基金会项目(项目编号 CRSII3_154488、310030_144219、310030_127356 和 310030_144219)以及 Christine Kühne - 过敏研究与教育中心(CK-CARE)的资助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c3c/7495089/396c3d9612d4/gr1.jpg

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