Department of Polymer Science and Engineering, Hefei National Research Center for Physical Sciences at the Microscale, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), University of Science and Technology of China, Hefei 230026, China
hjliang@ustc.edu.cn
收稿:2022-06-21,
修回:2022-7-17,
录用:2022-7-18,
网络首发:2022-09-21,
纸质出版:2023-03-01
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Zhou, J. X.; Yin, X.; Liang, H. J. An effective platform for SARS-CoV-2 prevention by combining neutralization and RNAi technology. Chinese J. Polym. Sci. 2023, 41, 327–333
Jun-Xiang Zhou, Xue Yin, Hao-Jun Liang. An Effective Platform for SARS-CoV-2 Prevention by Combining Neutralization and RNAi Technology[J]. Chinese Journal of Polymer Science, 2023, 41(3): 327-333.
Zhou, J. X.; Yin, X.; Liang, H. J. An effective platform for SARS-CoV-2 prevention by combining neutralization and RNAi technology. Chinese J. Polym. Sci. 2023, 41, 327–333 DOI: 10.1007/s10118-022-2846-6.
Jun-Xiang Zhou, Xue Yin, Hao-Jun Liang. An Effective Platform for SARS-CoV-2 Prevention by Combining Neutralization and RNAi Technology[J]. Chinese Journal of Polymer Science, 2023, 41(3): 327-333. DOI: 10.1007/s10118-022-2846-6.
A novel platform was established for prevention against the SARS-CoV-2 by utilizing a customized cell line. The pseudotyped SARS-CoV-2 was efficienly captured by the overexpressed ACE2 on the cell membrane. The subsequent viral replication and transcription processes could be blocked by the intracellular shRNAs designed as comlement to the viral genome fragments.
At present
the coronavirus disease 2019 (COVID-19) pandemic is a global health crisis. Scientists all over the globe are urgently looking forward to an effective solution to prevent the spread of the epidemic and avoid more casualties at an early date. In this study
we establish an effective platform for the prevention of SARS-CoV-2 by combining the neutralization strategy and RNAi technology. To protect normal cells from infection
the customized cells are constructed to stably express viral antigenic receptor ACE2 on the cell membrane. These modified cells are used as bait for inducing the viral entry. The transcription and replication activities of viral genome are intercepted subsequently by the intracellular shRNAs
which are complementary to the viral gene fragments. A pseudotyped virus reconstructed from the HIV lentivirus is utilized as a virus model
by which we validate the feasibility and effectiveness of our strategy
in vitro
. Our work establishes an initial model and lays the foundation for future prevention and treatment of various RNA viruses.
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