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10.1038/s41467-020-18058-8

http://scihub22266oqcxt.onion/10.1038/s41467-020-18058-8
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32826914!7442812!32826914
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suck abstract from ncbi


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pmid32826914      Nat+Commun 2020 ; 11 (1): 4198
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  • A cross-reactive human IgA monoclonal antibody blocks SARS-CoV-2 spike-ACE2 interaction #MMPMID32826914
  • Ejemel M; Li Q; Hou S; Schiller ZA; Tree JA; Wallace A; Amcheslavsky A; Kurt Yilmaz N; Buttigieg KR; Elmore MJ; Godwin K; Coombes N; Toomey JR; Schneider R; Ramchetty AS; Close BJ; Chen DY; Conway HL; Saeed M; Ganesa C; Carroll MW; Cavacini LA; Klempner MS; Schiffer CA; Wang Y
  • Nat Commun 2020[Aug]; 11 (1): 4198 PMID32826914show ga
  • COVID-19 caused by SARS-CoV-2 has become a global pandemic requiring the development of interventions for the prevention or treatment to curtail mortality and morbidity. No vaccine to boost mucosal immunity, or as a therapeutic, has yet been developed to SARS-CoV-2. In this study, we discover and characterize a cross-reactive human IgA monoclonal antibody, MAb362. MAb362 binds to both SARS-CoV and SARS-CoV-2 spike proteins and competitively blocks ACE2 receptor binding, by overlapping the ACE2 structural binding epitope. Furthermore, MAb362 IgA neutralizes both pseudotyped SARS-CoV and SARS-CoV-2 in 293 cells expressing ACE2. When converted to secretory IgA, MAb326 also neutralizes authentic SARS-CoV-2 virus while the IgG isotype shows no neutralization. Our results suggest that SARS-CoV-2 specific IgA antibodies, such as MAb362, may provide effective immunity against SARS-CoV-2 by inducing mucosal immunity within the respiratory system, a potentially critical feature of an effective vaccine.
  • |Angiotensin-Converting Enzyme 2[MESH]
  • |Animals[MESH]
  • |Antibodies, Monoclonal/*immunology/metabolism[MESH]
  • |Antibodies, Neutralizing/*immunology/metabolism[MESH]
  • |Betacoronavirus/*immunology[MESH]
  • |Chlorocebus aethiops[MESH]
  • |Cross Reactions[MESH]
  • |Epitopes[MESH]
  • |HEK293 Cells[MESH]
  • |Humans[MESH]
  • |Immunoglobulin A, Secretory/immunology/metabolism[MESH]
  • |Immunoglobulin A/*immunology/metabolism[MESH]
  • |Immunoglobulin G/immunology/metabolism[MESH]
  • |Models, Molecular[MESH]
  • |Mutation[MESH]
  • |Peptidyl-Dipeptidase A/*metabolism[MESH]
  • |Protein Binding[MESH]
  • |Protein Interaction Domains and Motifs[MESH]
  • |SARS-CoV-2[MESH]
  • |Severe acute respiratory syndrome-related coronavirus/immunology[MESH]
  • |Spike Glycoprotein, Coronavirus/chemistry/genetics/immunology/*metabolism[MESH]


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