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10.1093/abt/tbaa009

http://scihub22266oqcxt.onion/10.1093/abt/tbaa009
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32566896!7291920!32566896
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suck abstract from ncbi


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pmid32566896      Antib+Ther 2020 ; 3 (2): 109-114
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  • Perspectives on the development of neutralizing antibodies against SARS-CoV-2 #MMPMID32566896
  • Ho M
  • Antib Ther 2020[Apr]; 3 (2): 109-114 PMID32566896show ga
  • SARS-CoV-2 gains entry to human cells through its spike (S) protein binding to angiotensin-converting enzyme 2 (ACE2). Therefore, the receptor binding domain (RBD) of the S protein is the primary target for neutralizing antibodies. Selection of broad-neutralizing antibodies against SARS-CoV-2 and SARS-CoV is attractive and might be useful for treating not only COVID-19 but also future SARS-related CoV infections. Broad-neutralizing antibodies, such as 47D11, S309, and VHH-72, have been reported to target a conserved region in the RBD of the S1 subunit. The S2 subunit required for viral membrane fusion might be another target. Due to their small size and high stability, single-domain antibodies might have the ability to be administered by an inhaler making them potentially attractive therapeutics for respiratory infections. A cocktail strategy combining two (or more) antibodies that recognize different parts of the viral surface that interact with human cells might be the most effective.
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