细胞外小泡
诱饵
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)
肝素
2019-20冠状病毒爆发
共轭体系
病毒学
化学
医学
细胞生物学
生物
生物化学
传染病(医学专业)
爆发
病理
受体
聚合物
疾病
有机化学
作者
Bin Tu,Zhenzhen Pan,Huiyuan Wang,Jingkun Qu,Sun Fei-fei,Mingjie Shi,Yingyan Zhang,Han Wu,Bahtiyor Muhitdinov,Yongzhuo Huang
标识
DOI:10.1021/acsmaterialslett.3c01442
摘要
The very highly contagious Omicron variant of SARS-CoV-2, repeated infection, and long COVID symptoms continue to be a health threat with few convenient preventive or therapeutic methods suitable for common use. Spike-glycan interactions play an essential role in SARS-CoV-2 infections, and heparan sulfate acts as a coreceptor for mediating the cell entry of the virus. In response to this challenge, we proposed a dual-decoy strategy using both heparin (an analogue of heparan sulfate) and ACE2 to neutralize SARS-CoV-2. We developed a heparin-conjugated ACE2-bearing extracellular vesicle system (haEVs), serving as nano dual bait, with high efficiency in neutralizing the Omicron variant through interactions with the viral Spike protein. In vitro experiments showed that haEVs bound to the pseudovirus of SARS-CoV-2 and effectively prevented the pseudovirus infection of host cells. In vivo experiments further demonstrated that inhalable haEVs effectively blocked the pseudovirus infection of lung tissue of the Omicron variant with good biosafety. This dual-decoy approach presents a promising avenue for combating SARS-CoV-2, especially the Omicron variant, with the advantage of self-administration for preventive and therapeutic applications.
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