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三维组织平台用于研究甲型流感病毒和严重急性呼吸综合征冠状病毒 2 引起的呼吸道疾病的早期阶段。

3D tissue platforms to investigate the early phases of influenza a virus- and SARS-CoV-2-induced respiratory diseases.

机构信息

Institute-Associated Research Group "Regulatory Mechanisms of Inflammation", Institute of Medical Biochemistry, Center for Molecular Biology of Inflammation, and "Cells in Motion" Interfaculty Center, University of Münster, Münster, Germany.

Leibniz Institute of Virology, Hamburg, Germany.

出版信息

Emerg Microbes Infect. 2022 Dec;11(1):2160-2175. doi: 10.1080/22221751.2022.2117101.

Abstract

Pandemic outbreaks of viruses such as influenza virus or SARS-CoV-2 are associated with high morbidity and mortality and thus pose a massive threat to global health and economics. Physiologically relevant models are needed to study the viral life cycle, describe the pathophysiological consequences of viral infection, and explore possible drug targets and treatment options. While simple cell culture-based models do not reflect the tissue environment and systemic responses, animal models are linked with huge direct and indirect costs and ethical questions. platforms based on tissue explants have been introduced as suitable platforms to bridge the gap between cell culture and animal models. We established a murine lung tissue explant platform for two respiratory viruses, influenza A virus (IAV) and SARS-CoV-2. We observed efficient viral replication, associated with the release of inflammatory cytokines and the induction of an antiviral interferon response, comparable to infection in human lung explants. Endolysosomal entry could be confirmed as a potential host target for pharmacological intervention, and the potential repurposing potentials of fluoxetine and interferons for host-directed therapy previously seen could be recapitulated in the model.

摘要

病毒(如流感病毒或 SARS-CoV-2)引发的大流行疫情与高发病率和死亡率相关,因此对全球健康和经济构成了巨大威胁。需要生理相关的模型来研究病毒生命周期、描述病毒感染的病理生理后果,并探索可能的药物靶点和治疗方案。虽然基于简单细胞培养的模型不能反映组织环境和全身反应,但动物模型存在巨大的直接和间接成本以及伦理问题。基于组织外植体的平台已被引入作为细胞培养和动物模型之间的桥梁。我们建立了一个用于两种呼吸道病毒(流感病毒[IAV]和 SARS-CoV-2)的鼠肺组织外植体平台。我们观察到有效的病毒复制,伴随着炎症细胞因子的释放和抗病毒干扰素反应的诱导,与人类肺外植体感染相当。内体溶酶体进入可以被确认为潜在的宿主药物靶点,并且先前在 IAV 模型中观察到的氟西汀和干扰素的重新利用潜力可以在 SARS-CoV-2 模型中重现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3302/9518268/fa873ee14ba4/TEMI_A_2117101_F0001_OC.jpg

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