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一种用于H1N1和SARS-CoV-2感染及抗病毒筛选的新型体外原代人肺泡模型(AlveolAir™)

A Novel In Vitro Primary Human Alveolar Model (AlveolAir™) for H1N1 and SARS-CoV-2 Infection and Antiviral Screening.

作者信息

Lopes Cindia Ferreira, Laurent Emilie, Caul-Futy Mireille, Dubois Julia, Mialon Chloé, Chojnacki Caroline, Sage Edouard, Boda Bernadett, Huang Song, Rosa-Calatrava Manuel, Constant Samuel

机构信息

Epithelix,1228 Geneva, Switzerland.

CIRI, Centre International de Recherche en Infectiologie, Team VirPath, Inserm, Université Claude Bernard Lyon 1, CNRS, UMR5308, ENS de Lyon, 69007 Lyon, France.

出版信息

Microorganisms. 2025 Mar 3;13(3):572. doi: 10.3390/microorganisms13030572.

DOI:10.3390/microorganisms13030572
PMID:40142465
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11944821/
Abstract

Lower respiratory infections, mostly caused by viral or bacterial pathogens, remain a leading global cause of mortality. The differences between animal models and humans contribute to inefficiencies in drug development, highlighting the need for more relevant and predictive, non-animal models. In this context, AlveolAir™, a fully primary in vitro 3D human alveolar model, was characterized and demonstrated the sustained presence of alveolar type I (ATI) and type II (ATII) cells. This model exhibited a functional barrier over a 30-day period, evidenced by high transepithelial electrical resistance (TEER). These findings were further validated by tight junctions' confocal microscopy and low permeability to Lucifer yellow, confirming AlveolAir™ as robust platform for drug transport assays. Additionally, successful infections with H1N1 and SARS-CoV-2 viruses were achieved, and antiviral treatments with Baloxavir and Remdesivir, respectively, effectively reduced viral replication. Interestingly, both viruses infected only the epithelial layer without replicating in endothelial cells. These findings indicate AlveolAir™ as a relevant model for assessing the toxicity and permeability of xenobiotics and evaluating the efficacy of novel antiviral therapies.

摘要

下呼吸道感染主要由病毒或细菌病原体引起,仍然是全球主要的死亡原因。动物模型与人类之间的差异导致药物开发效率低下,这凸显了对更相关、更具预测性的非动物模型的需求。在此背景下,对完全原代的体外3D人肺泡模型AlveolAir™进行了表征,并证明了肺泡I型(ATI)和II型(ATII)细胞的持续存在。该模型在30天内表现出功能性屏障,高跨上皮电阻(TEER)证明了这一点。这些发现通过紧密连接的共聚焦显微镜和对荧光素黄的低渗透性得到进一步验证,证实AlveolAir™是用于药物转运测定的强大平台。此外,成功实现了H1N1和SARS-CoV-2病毒感染,分别用巴洛沙韦和瑞德西韦进行抗病毒治疗有效降低了病毒复制。有趣的是,两种病毒都仅感染上皮层,而不在内皮细胞中复制。这些发现表明AlveolAir™是评估异种生物毒性和渗透性以及评估新型抗病毒疗法疗效的相关模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4f2/11944821/4c364e7ca5ff/microorganisms-13-00572-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4f2/11944821/6a6232626621/microorganisms-13-00572-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4f2/11944821/a808073317df/microorganisms-13-00572-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4f2/11944821/615af3ddcf66/microorganisms-13-00572-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4f2/11944821/1433e8672c12/microorganisms-13-00572-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4f2/11944821/4c364e7ca5ff/microorganisms-13-00572-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4f2/11944821/6a6232626621/microorganisms-13-00572-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4f2/11944821/a808073317df/microorganisms-13-00572-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4f2/11944821/615af3ddcf66/microorganisms-13-00572-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4f2/11944821/1433e8672c12/microorganisms-13-00572-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4f2/11944821/4c364e7ca5ff/microorganisms-13-00572-g005.jpg

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本文引用的文献

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Alveolar epithelial cells mitigate neutrophilic inflammation in lung injury through regulating mitochondrial fatty acid oxidation.肺泡上皮细胞通过调节线粒体脂肪酸氧化减轻肺损伤中的中性粒细胞炎症。
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精准切取肺切片:用于研究肺生理学、药理学、疾病发病机制和药物发现的一体化离体模型。
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