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10.1080/21645515.2020.1787066

http://scihub22266oqcxt.onion/10.1080/21645515.2020.1787066
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32663051!7872019!32663051
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suck abstract from ncbi


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pmid32663051      Hum+Vaccin+Immunother 2021 ; 17 (1): 92-97
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  • An immunotherapeutic method for COVID-19 patients: a soluble ACE2-Anti-CD16 VHH to block SARS-CoV-2 Spike protein #MMPMID32663051
  • Sheikhi A; Hojjat-Farsangi M
  • Hum Vaccin Immunother 2021[Jan]; 17 (1): 92-97 PMID32663051show ga
  • The third outbreak of coronavirus (CoV) infection (after SARS-CoV and MERS-CoV) caused by a novel CoV (SARS-CoV-2) of the genus Beta-coronavirus has become a global pandemic. CoVs are enveloped viruses whose proteins include spike (S), membrane (M), and envelope (E) which are embedded in the viral envelope. The glycosylated S protein, which forms homo-trimeric spikes on the surface of the viral particle, mediates viral entry into host cells. SARS-CoV-2, like SARS-CoV, uses the Angiotensin-Converting Enzyme 2 (ACE2) cell surface protein for cellular entry. An attractive anti-viral approach is targeting virus entry into cells, for which three strategies are suggested: 1) direct targeting of the viral glycoprotein; 2) targeting the viral receptor on the cell surface; and 3) using soluble (s) ACE2 that binds to S protein thereby neutralizing the virus. In this article, the advantages and disadvantages of these strategies are explained. Moreover, we propose that fusion of the sACE2 to anti-CD16 to produce a bi-speci fi c molecule could be a promising anti-viral strategy.
  • |Angiotensin-Converting Enzyme 2/*metabolism[MESH]
  • |Antibodies, Neutralizing/metabolism[MESH]
  • |COVID-19/*immunology/metabolism/*prevention & control[MESH]
  • |Coronavirus Infections/*immunology/metabolism/*prevention & control[MESH]
  • |Humans[MESH]
  • |Protein Binding[MESH]


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