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10.1038/s41586-020-2349-y

http://scihub22266oqcxt.onion/10.1038/s41586-020-2349-y
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32422645!ä!32422645

suck abstract from ncbi


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pmid32422645      Nature 2020 ; 583 (7815): 290-295
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  • Cross-neutralization of SARS-CoV-2 by a human monoclonal SARS-CoV antibody #MMPMID32422645
  • Pinto D; Park YJ; Beltramello M; Walls AC; Tortorici MA; Bianchi S; Jaconi S; Culap K; Zatta F; De Marco A; Peter A; Guarino B; Spreafico R; Cameroni E; Case JB; Chen RE; Havenar-Daughton C; Snell G; Telenti A; Virgin HW; Lanzavecchia A; Diamond MS; Fink K; Veesler D; Corti D
  • Nature 2020[Jul]; 583 (7815): 290-295 PMID32422645show ga
  • Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a newly emerged coronavirus that is responsible for the current pandemic of coronavirus disease 2019 (COVID-19), which has resulted in more than 3.7 million infections and 260,000 deaths as of 6 May 2020(1,2). Vaccine and therapeutic discovery efforts are paramount to curb the pandemic spread of this zoonotic virus. The SARS-CoV-2 spike (S) glycoprotein promotes entry into host cells and is the main target of neutralizing antibodies. Here we describe several monoclonal antibodies that target the S glycoprotein of SARS-CoV-2, which we identified from memory B cells of an individual who was infected with severe acute respiratory syndrome coronavirus (SARS-CoV) in 2003. One antibody (named S309) potently neutralizes SARS-CoV-2 and SARS-CoV pseudoviruses as well as authentic SARS-CoV-2, by engaging the receptor-binding domain of the S glycoprotein. Using cryo-electron microscopy and binding assays, we show that S309 recognizes an epitope containing a glycan that is conserved within the Sarbecovirus subgenus, without competing with receptor attachment. Antibody cocktails that include S309 in combination with other antibodies that we identified further enhanced SARS-CoV-2 neutralization, and may limit the emergence of neutralization-escape mutants. These results pave the way for using S309 and antibody cocktails containing S309 for prophylaxis in individuals at a high risk of exposure or as a post-exposure therapy to limit or treat severe disease.
  • |Angiotensin-Converting Enzyme 2[MESH]
  • |Animals[MESH]
  • |Antibodies, Monoclonal/chemistry/*immunology/pharmacology[MESH]
  • |Antibodies, Neutralizing/chemistry/*immunology/pharmacology[MESH]
  • |Antibodies, Viral/chemistry/immunology/pharmacology[MESH]
  • |Antibody-Dependent Cell Cytotoxicity/drug effects/immunology[MESH]
  • |B-Lymphocytes/immunology[MESH]
  • |Betacoronavirus/chemistry/drug effects/*immunology[MESH]
  • |COVID-19[MESH]
  • |Chlorocebus aethiops[MESH]
  • |Coronavirus Infections/immunology/prevention & control/therapy/virology[MESH]
  • |Cross Reactions/drug effects/*immunology[MESH]
  • |Cryoelectron Microscopy[MESH]
  • |Epitopes, B-Lymphocyte/chemistry/immunology[MESH]
  • |HEK293 Cells[MESH]
  • |Humans[MESH]
  • |Immune Evasion/immunology[MESH]
  • |Immunoglobulin Fab Fragments/chemistry/immunology/pharmacology[MESH]
  • |Immunologic Memory/immunology[MESH]
  • |Killer Cells, Natural/drug effects/immunology[MESH]
  • |Models, Molecular[MESH]
  • |Neutralization Tests[MESH]
  • |Pandemics/prevention & control[MESH]
  • |Peptidyl-Dipeptidase A/chemistry/metabolism[MESH]
  • |Pneumonia, Viral/immunology/prevention & control/therapy/virology[MESH]
  • |SARS-CoV-2[MESH]
  • |Severe Acute Respiratory Syndrome/*immunology/virology[MESH]
  • |Severe acute respiratory syndrome-related coronavirus/chemistry/drug effects/*immunology[MESH]
  • |Spike Glycoprotein, Coronavirus/chemistry/*immunology[MESH]


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