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利用细菌提取物进行固有免疫训练可增强肺部巨噬细胞募集,以预防β冠状病毒感染。

Innate Immune Training with Bacterial Extracts Enhances Lung Macrophage Recruitment to Protect from Betacoronavirus Infection.

机构信息

Department of Internal Medicine II/Cardiology, Medical University of Vienna, Vienna, Austria.

Ludwig Boltzmann Cluster for Cardiovascular Research, Vienna, Austria.

出版信息

J Innate Immun. 2022;14(4):293-305. doi: 10.1159/000519699. Epub 2021 Nov 12.

Abstract

Training of the innate immune system with orally ingested bacterial extracts was demonstrated to have beneficial effects on infection clearance and disease outcome. The aim of our study was to identify cellular and molecular processes responsible for these immunological benefits. We used a murine coronavirus (MCoV) A59 mouse model treated with the immune activating bacterial extract Broncho-Vaxom (BV) OM-85. Tissue samples were analysed with qPCR, RNA sequencing, histology, and flow cytometry. After BV OM-85 treatment, interstitial macrophages accumulated in lung tissue leading to a faster response of type I interferon (IFN) signalling after MCoV infection resulting in overall lung tissue protection. Moreover, RNA sequencing showed that lung tissue from mice receiving BV OM-85 resembled an intermediate stage between healthy and viral infected lung tissue at day 4, indicating a faster return to normal tissue homoeostasis. The pharmacologic effect was mimicked by adoptively transferring naive lung macrophages into lungs from recipient mice before virus infection. The beneficial effect of BV OM-85 was abolished when inhibiting initial type I IFN signalling. Overall, our data suggest that BV OM-85 enhances lung macrophages allowing for a faster IFN response towards a viral challenge as part of the oral-induced innate immune system training.

摘要

经口服摄入细菌提取物训练先天免疫系统已被证明对清除感染和改善疾病预后具有有益效果。我们研究的目的是确定负责这些免疫益处的细胞和分子过程。我们使用了一种感染鼠冠状病毒(MCoV)A59 的小鼠模型,并用免疫激活细菌提取物 Broncho-Vaxom(BV)OM-85 进行处理。使用 qPCR、RNA 测序、组织学和流式细胞术分析组织样本。在接受 BV OM-85 治疗后,间质性巨噬细胞在肺部组织中积聚,导致在 MCoV 感染后更快地响应 I 型干扰素(IFN)信号,从而对肺部组织整体起到保护作用。此外,RNA 测序显示,接受 BV OM-85 治疗的小鼠肺部组织在第 4 天与健康和病毒感染肺部组织之间呈现中间阶段,表明更快地恢复到正常组织稳态。在病毒感染前将幼稚肺巨噬细胞过继转移到受体小鼠的肺部,可以模拟这种药理作用。当抑制初始 I 型 IFN 信号时,BV OM-85 的有益作用被消除。总的来说,我们的数据表明,BV OM-85 增强了肺巨噬细胞,使其能够更快地对病毒挑战产生 IFN 反应,这是口服诱导的先天免疫系统训练的一部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/696a/9274953/9b2a517df5d9/jin-0014-0293-g01.jpg

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