吸入
肺
冠状病毒
2019年冠状病毒病(COVID-19)
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
病毒学
发病机制
大流行
病毒
医学
冠状病毒科
免疫学
病理
疾病
传染病(医学专业)
麻醉
内科学
作者
Zhenhua Li,Zhenzhen Wang,Phuong‐Uyen Dinh,Dashuai Zhu,Kristen D. Popowski,Halle Lutz,Shiqi Hu,Mark G. Lewis,Anthony Cook,Hanné Andersen,Jack Greenhouse,Laurent Pessaint,Leonard J. Lobo,Ke Cheng
标识
DOI:10.1038/s41565-021-00923-2
摘要
Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has grown into a global pandemic, and only a few antiviral treatments have been approved to date. Angiotensin-converting enzyme 2 (ACE2) plays a fundamental role in SARS-CoV-2 pathogenesis because it allows viral entry into host cells. Here we show that ACE2 nanodecoys derived from human lung spheroid cells (LSCs) can bind and neutralize SARS-CoV-2 and protect the host lung cells from infection. In mice, these LSC-nanodecoys were delivered via inhalation therapy and resided in the lungs for over 72 h post-delivery. Furthermore, inhalation of the LSC-nanodecoys accelerated clearance of SARS-CoV-2 mimics from the lungs, with no observed toxicity. In cynomolgus macaques challenged with live SARS-CoV-2, four doses of these nanodecoys delivered by inhalation promoted viral clearance and reduced lung injury. Our results suggest that LSC-nanodecoys can serve as a potential therapeutic agent for treating COVID-19.
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