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Details

Autor(en) / Beteiligte
Titel
Cross-neutralization of SARS-CoV-2 by a human monoclonal SARS-CoV antibody
Ist Teil von
  • Nature (London), 2020-07, Vol.583 (7815), p.290-295
Ort / Verlag
London: Nature Publishing Group UK
Erscheinungsjahr
2020
Quelle
MEDLINE
Beschreibungen/Notizen
  • 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. The monoclonal antibody S309, identified from memory B cells of an individual infected with SARS-CoV in 2003, or antibody cocktails that contain this antibody potently neutralize SARS-CoV-2.
Sprache
Englisch
Identifikatoren
ISSN: 0028-0836
eISSN: 1476-4687
DOI: 10.1038/s41586-020-2349-y
Titel-ID: cdi_hal_primary_oai_HAL_pasteur_02623374v1
Format
Schlagworte
101/28, 13/1, 13/31, 631/250/255/2514, 631/326/596/4130, 631/61/51/1568, Angiotensin-Converting Enzyme 2, Animals, Antibodies, Antibodies, Monoclonal - chemistry, Antibodies, Monoclonal - immunology, Antibodies, Monoclonal - pharmacology, Antibodies, Neutralizing - chemistry, Antibodies, Neutralizing - immunology, Antibodies, Neutralizing - pharmacology, Antibodies, Viral - chemistry, Antibodies, Viral - immunology, Antibodies, Viral - pharmacology, Antibody-Dependent Cell Cytotoxicity - drug effects, Antibody-Dependent Cell Cytotoxicity - immunology, B-Lymphocytes - immunology, Betacoronavirus - chemistry, Betacoronavirus - drug effects, Betacoronavirus - immunology, Binding, Chlorocebus aethiops, Coronaviridae, Coronavirus Infections - immunology, Coronavirus Infections - prevention & control, Coronavirus Infections - therapy, Coronavirus Infections - virology, Coronaviruses, COVID-19, Cross Reactions - drug effects, Cross Reactions - immunology, Cryoelectron Microscopy, Disease transmission, Electron microscopy, Enzymes, Epidemics, Epitopes, Epitopes, B-Lymphocyte - chemistry, Epitopes, B-Lymphocyte - immunology, Glycan, Glycoproteins, HEK293 Cells, Humanities and Social Sciences, Humans, Immune Evasion - immunology, Immunoglobulin Fab Fragments - chemistry, Immunoglobulin Fab Fragments - immunology, Immunoglobulin Fab Fragments - pharmacology, Immunologic Memory - immunology, Immunological memory, Killer Cells, Natural - drug effects, Killer Cells, Natural - immunology, Life Sciences, Lymphocytes B, Memory cells, Microscopy, Middle East respiratory syndrome, Models, Molecular, Monoclonal antibodies, multidisciplinary, Neutralization, Neutralization Tests, Pandemics, Pandemics - prevention & control, Peptidyl-Dipeptidase A - chemistry, Peptidyl-Dipeptidase A - metabolism, Pneumonia, Viral - immunology, Pneumonia, Viral - prevention & control, Pneumonia, Viral - therapy, Pneumonia, Viral - virology, Prophylaxis, Receptors, Respiratory diseases, Sarbecovirus, SARS Virus - chemistry, SARS Virus - drug effects, SARS Virus - immunology, SARS-CoV-2, Science, Science (multidisciplinary), Severe Acute Respiratory Syndrome - immunology, Severe Acute Respiratory Syndrome - virology, Severe acute respiratory syndrome coronavirus 2, Spike Glycoprotein, Coronavirus - chemistry, Spike Glycoprotein, Coronavirus - immunology, Vaccines, Vero Cells, Viral diseases, Viruses, Zoonoses

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