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Human neutralizing antibodies to cold linear epitopes and to subdomain 1 of SARS-CoV-2
Emergence of SARS-CoV-2 variants diminishes the efficacy of vaccines and antiviral monoclonal antibodies. Continued development of immunotherapies and vaccine immunogens resilient to viral evolution is therefore necessary. Using coldspot-guided antibody discovery, a screening approach that focuses o...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727766/ https://www.ncbi.nlm.nih.gov/pubmed/36482967 http://dx.doi.org/10.1101/2022.11.24.515932 |
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author | Bianchini, Filippo Crivelli, Virginia Abernathy, Morgan E. Guerra, Concetta Palus, Martin Muri, Jonathan Marcotte, Harold Piralla, Antonio Pedotti, Mattia De Gasparo, Raoul Simonelli, Luca Matkovic, Milos Toscano, Chiara Biggiogero, Maira Calvaruso, Veronica Svoboda, Pavel Rincón, Tomás Cervantes Fava, Tommaso Podešvová, Lucie Shanbhag, Akanksha A. Celoria, Andrea Sgrignani, Jacopo Stefanik, Michal Hönig, Vaclav Pranclova, Veronika Michalcikova, Tereza Prochazka, Jan Guerrini, Giuditta Mehn, Dora Ciabattini, Annalisa Abolhassani, Hassan Jarrossay, David Uguccioni, Mariagrazia Medaglini, Donata Pan-Hammarström, Qiang Calzolai, Luigi Fernandez, Daniel Baldanti, Fausto Franzetti-Pellanda, Alessandra Garzoni, Christian Sedlacek, Radislav Ruzek, Daniel Varani, Luca Cavalli, Andrea Barnes, Christopher O. Robbiani, Davide F. |
author_facet | Bianchini, Filippo Crivelli, Virginia Abernathy, Morgan E. Guerra, Concetta Palus, Martin Muri, Jonathan Marcotte, Harold Piralla, Antonio Pedotti, Mattia De Gasparo, Raoul Simonelli, Luca Matkovic, Milos Toscano, Chiara Biggiogero, Maira Calvaruso, Veronica Svoboda, Pavel Rincón, Tomás Cervantes Fava, Tommaso Podešvová, Lucie Shanbhag, Akanksha A. Celoria, Andrea Sgrignani, Jacopo Stefanik, Michal Hönig, Vaclav Pranclova, Veronika Michalcikova, Tereza Prochazka, Jan Guerrini, Giuditta Mehn, Dora Ciabattini, Annalisa Abolhassani, Hassan Jarrossay, David Uguccioni, Mariagrazia Medaglini, Donata Pan-Hammarström, Qiang Calzolai, Luigi Fernandez, Daniel Baldanti, Fausto Franzetti-Pellanda, Alessandra Garzoni, Christian Sedlacek, Radislav Ruzek, Daniel Varani, Luca Cavalli, Andrea Barnes, Christopher O. Robbiani, Davide F. |
author_sort | Bianchini, Filippo |
collection | PubMed |
description | Emergence of SARS-CoV-2 variants diminishes the efficacy of vaccines and antiviral monoclonal antibodies. Continued development of immunotherapies and vaccine immunogens resilient to viral evolution is therefore necessary. Using coldspot-guided antibody discovery, a screening approach that focuses on portions of the virus spike that are both functionally relevant and averse to change, we identified human neutralizing antibodies to highly conserved viral epitopes. Antibody fp.006 binds the fusion peptide and cross-reacts against coronaviruses of the four genera, including the nine human coronaviruses, through recognition of a conserved motif that includes the S2´ site of proteolytic cleavage. Antibody hr2.016 targets the stem helix and neutralizes SARS-CoV-2 variants. Antibody sd1.040 binds to subdomain 1, synergizes with antibody rbd.042 for neutralization and, like fp.006 and hr2.016, protects mice when present as bispecific antibody. Thus, coldspot-guided antibody discovery reveals donor-derived neutralizing antibodies that are cross-reactive with Orthocoronavirinae, including SARS-CoV-2 variants. |
format | Online Article Text |
id | pubmed-9727766 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-97277662022-12-08 Human neutralizing antibodies to cold linear epitopes and to subdomain 1 of SARS-CoV-2 Bianchini, Filippo Crivelli, Virginia Abernathy, Morgan E. Guerra, Concetta Palus, Martin Muri, Jonathan Marcotte, Harold Piralla, Antonio Pedotti, Mattia De Gasparo, Raoul Simonelli, Luca Matkovic, Milos Toscano, Chiara Biggiogero, Maira Calvaruso, Veronica Svoboda, Pavel Rincón, Tomás Cervantes Fava, Tommaso Podešvová, Lucie Shanbhag, Akanksha A. Celoria, Andrea Sgrignani, Jacopo Stefanik, Michal Hönig, Vaclav Pranclova, Veronika Michalcikova, Tereza Prochazka, Jan Guerrini, Giuditta Mehn, Dora Ciabattini, Annalisa Abolhassani, Hassan Jarrossay, David Uguccioni, Mariagrazia Medaglini, Donata Pan-Hammarström, Qiang Calzolai, Luigi Fernandez, Daniel Baldanti, Fausto Franzetti-Pellanda, Alessandra Garzoni, Christian Sedlacek, Radislav Ruzek, Daniel Varani, Luca Cavalli, Andrea Barnes, Christopher O. Robbiani, Davide F. bioRxiv Article Emergence of SARS-CoV-2 variants diminishes the efficacy of vaccines and antiviral monoclonal antibodies. Continued development of immunotherapies and vaccine immunogens resilient to viral evolution is therefore necessary. Using coldspot-guided antibody discovery, a screening approach that focuses on portions of the virus spike that are both functionally relevant and averse to change, we identified human neutralizing antibodies to highly conserved viral epitopes. Antibody fp.006 binds the fusion peptide and cross-reacts against coronaviruses of the four genera, including the nine human coronaviruses, through recognition of a conserved motif that includes the S2´ site of proteolytic cleavage. Antibody hr2.016 targets the stem helix and neutralizes SARS-CoV-2 variants. Antibody sd1.040 binds to subdomain 1, synergizes with antibody rbd.042 for neutralization and, like fp.006 and hr2.016, protects mice when present as bispecific antibody. Thus, coldspot-guided antibody discovery reveals donor-derived neutralizing antibodies that are cross-reactive with Orthocoronavirinae, including SARS-CoV-2 variants. Cold Spring Harbor Laboratory 2022-11-28 /pmc/articles/PMC9727766/ /pubmed/36482967 http://dx.doi.org/10.1101/2022.11.24.515932 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Bianchini, Filippo Crivelli, Virginia Abernathy, Morgan E. Guerra, Concetta Palus, Martin Muri, Jonathan Marcotte, Harold Piralla, Antonio Pedotti, Mattia De Gasparo, Raoul Simonelli, Luca Matkovic, Milos Toscano, Chiara Biggiogero, Maira Calvaruso, Veronica Svoboda, Pavel Rincón, Tomás Cervantes Fava, Tommaso Podešvová, Lucie Shanbhag, Akanksha A. Celoria, Andrea Sgrignani, Jacopo Stefanik, Michal Hönig, Vaclav Pranclova, Veronika Michalcikova, Tereza Prochazka, Jan Guerrini, Giuditta Mehn, Dora Ciabattini, Annalisa Abolhassani, Hassan Jarrossay, David Uguccioni, Mariagrazia Medaglini, Donata Pan-Hammarström, Qiang Calzolai, Luigi Fernandez, Daniel Baldanti, Fausto Franzetti-Pellanda, Alessandra Garzoni, Christian Sedlacek, Radislav Ruzek, Daniel Varani, Luca Cavalli, Andrea Barnes, Christopher O. Robbiani, Davide F. Human neutralizing antibodies to cold linear epitopes and to subdomain 1 of SARS-CoV-2 |
title | Human neutralizing antibodies to cold linear epitopes and to subdomain 1 of SARS-CoV-2 |
title_full | Human neutralizing antibodies to cold linear epitopes and to subdomain 1 of SARS-CoV-2 |
title_fullStr | Human neutralizing antibodies to cold linear epitopes and to subdomain 1 of SARS-CoV-2 |
title_full_unstemmed | Human neutralizing antibodies to cold linear epitopes and to subdomain 1 of SARS-CoV-2 |
title_short | Human neutralizing antibodies to cold linear epitopes and to subdomain 1 of SARS-CoV-2 |
title_sort | human neutralizing antibodies to cold linear epitopes and to subdomain 1 of sars-cov-2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727766/ https://www.ncbi.nlm.nih.gov/pubmed/36482967 http://dx.doi.org/10.1101/2022.11.24.515932 |
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