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Nanobody cocktails potently neutralize SARS-CoV-2 D614G N501Y variant and protect mice

Neutralizing antibodies are important for immunity against SARS-CoV-2 and as therapeutics for the prevention and treatment of COVID-19. Here, we identified high-affinity nanobodies from alpacas immunized with coronavirus spike and receptor-binding domains (RBD) that disrupted RBD engagement with the...

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Autores principales: Pymm, Phillip, Adair, Amy, Chan, Li-Jin, Cooney, James P., Mordant, Francesca L., Allison, Cody C., Lopez, Ester, Haycroft, Ebene R., O’Neill, Matthew T., Tan, Li Lynn, Dietrich, Melanie H., Drew, Damien, Doerflinger, Marcel, Dengler, Michael A., Scott, Nichollas E., Wheatley, Adam K., Gherardin, Nicholas A., Venugopal, Hariprasad, Cromer, Deborah, Davenport, Miles P., Pickering, Raelene, Godfrey, Dale I., Purcell, Damian F. J., Kent, Stephen J., Chung, Amy W., Subbarao, Kanta, Pellegrini, Marc, Glukhova, Alisa, Tham, Wai-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8126837/
https://www.ncbi.nlm.nih.gov/pubmed/33893175
http://dx.doi.org/10.1073/pnas.2101918118
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author Pymm, Phillip
Adair, Amy
Chan, Li-Jin
Cooney, James P.
Mordant, Francesca L.
Allison, Cody C.
Lopez, Ester
Haycroft, Ebene R.
O’Neill, Matthew T.
Tan, Li Lynn
Dietrich, Melanie H.
Drew, Damien
Doerflinger, Marcel
Dengler, Michael A.
Scott, Nichollas E.
Wheatley, Adam K.
Gherardin, Nicholas A.
Venugopal, Hariprasad
Cromer, Deborah
Davenport, Miles P.
Pickering, Raelene
Godfrey, Dale I.
Purcell, Damian F. J.
Kent, Stephen J.
Chung, Amy W.
Subbarao, Kanta
Pellegrini, Marc
Glukhova, Alisa
Tham, Wai-Hong
author_facet Pymm, Phillip
Adair, Amy
Chan, Li-Jin
Cooney, James P.
Mordant, Francesca L.
Allison, Cody C.
Lopez, Ester
Haycroft, Ebene R.
O’Neill, Matthew T.
Tan, Li Lynn
Dietrich, Melanie H.
Drew, Damien
Doerflinger, Marcel
Dengler, Michael A.
Scott, Nichollas E.
Wheatley, Adam K.
Gherardin, Nicholas A.
Venugopal, Hariprasad
Cromer, Deborah
Davenport, Miles P.
Pickering, Raelene
Godfrey, Dale I.
Purcell, Damian F. J.
Kent, Stephen J.
Chung, Amy W.
Subbarao, Kanta
Pellegrini, Marc
Glukhova, Alisa
Tham, Wai-Hong
author_sort Pymm, Phillip
collection PubMed
description Neutralizing antibodies are important for immunity against SARS-CoV-2 and as therapeutics for the prevention and treatment of COVID-19. Here, we identified high-affinity nanobodies from alpacas immunized with coronavirus spike and receptor-binding domains (RBD) that disrupted RBD engagement with the human receptor angiotensin-converting enzyme 2 (ACE2) and potently neutralized SARS-CoV-2. Epitope mapping, X-ray crystallography, and cryo-electron microscopy revealed two distinct antigenic sites and showed two neutralizing nanobodies from different epitope classes bound simultaneously to the spike trimer. Nanobody-Fc fusions of the four most potent nanobodies blocked ACE2 engagement with RBD variants present in human populations and potently neutralized both wild-type SARS-CoV-2 and the N501Y D614G variant at concentrations as low as 0.1 nM. Prophylactic administration of either single nanobody-Fc or as mixtures reduced viral loads by up to 10(4)-fold in mice infected with the N501Y D614G SARS-CoV-2 virus. These results suggest a role for nanobody-Fc fusions as prophylactic agents against SARS-CoV-2.
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spelling pubmed-81268372021-05-21 Nanobody cocktails potently neutralize SARS-CoV-2 D614G N501Y variant and protect mice Pymm, Phillip Adair, Amy Chan, Li-Jin Cooney, James P. Mordant, Francesca L. Allison, Cody C. Lopez, Ester Haycroft, Ebene R. O’Neill, Matthew T. Tan, Li Lynn Dietrich, Melanie H. Drew, Damien Doerflinger, Marcel Dengler, Michael A. Scott, Nichollas E. Wheatley, Adam K. Gherardin, Nicholas A. Venugopal, Hariprasad Cromer, Deborah Davenport, Miles P. Pickering, Raelene Godfrey, Dale I. Purcell, Damian F. J. Kent, Stephen J. Chung, Amy W. Subbarao, Kanta Pellegrini, Marc Glukhova, Alisa Tham, Wai-Hong Proc Natl Acad Sci U S A Biological Sciences Neutralizing antibodies are important for immunity against SARS-CoV-2 and as therapeutics for the prevention and treatment of COVID-19. Here, we identified high-affinity nanobodies from alpacas immunized with coronavirus spike and receptor-binding domains (RBD) that disrupted RBD engagement with the human receptor angiotensin-converting enzyme 2 (ACE2) and potently neutralized SARS-CoV-2. Epitope mapping, X-ray crystallography, and cryo-electron microscopy revealed two distinct antigenic sites and showed two neutralizing nanobodies from different epitope classes bound simultaneously to the spike trimer. Nanobody-Fc fusions of the four most potent nanobodies blocked ACE2 engagement with RBD variants present in human populations and potently neutralized both wild-type SARS-CoV-2 and the N501Y D614G variant at concentrations as low as 0.1 nM. Prophylactic administration of either single nanobody-Fc or as mixtures reduced viral loads by up to 10(4)-fold in mice infected with the N501Y D614G SARS-CoV-2 virus. These results suggest a role for nanobody-Fc fusions as prophylactic agents against SARS-CoV-2. National Academy of Sciences 2021-05-11 2021-04-23 /pmc/articles/PMC8126837/ /pubmed/33893175 http://dx.doi.org/10.1073/pnas.2101918118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Pymm, Phillip
Adair, Amy
Chan, Li-Jin
Cooney, James P.
Mordant, Francesca L.
Allison, Cody C.
Lopez, Ester
Haycroft, Ebene R.
O’Neill, Matthew T.
Tan, Li Lynn
Dietrich, Melanie H.
Drew, Damien
Doerflinger, Marcel
Dengler, Michael A.
Scott, Nichollas E.
Wheatley, Adam K.
Gherardin, Nicholas A.
Venugopal, Hariprasad
Cromer, Deborah
Davenport, Miles P.
Pickering, Raelene
Godfrey, Dale I.
Purcell, Damian F. J.
Kent, Stephen J.
Chung, Amy W.
Subbarao, Kanta
Pellegrini, Marc
Glukhova, Alisa
Tham, Wai-Hong
Nanobody cocktails potently neutralize SARS-CoV-2 D614G N501Y variant and protect mice
title Nanobody cocktails potently neutralize SARS-CoV-2 D614G N501Y variant and protect mice
title_full Nanobody cocktails potently neutralize SARS-CoV-2 D614G N501Y variant and protect mice
title_fullStr Nanobody cocktails potently neutralize SARS-CoV-2 D614G N501Y variant and protect mice
title_full_unstemmed Nanobody cocktails potently neutralize SARS-CoV-2 D614G N501Y variant and protect mice
title_short Nanobody cocktails potently neutralize SARS-CoV-2 D614G N501Y variant and protect mice
title_sort nanobody cocktails potently neutralize sars-cov-2 d614g n501y variant and protect mice
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8126837/
https://www.ncbi.nlm.nih.gov/pubmed/33893175
http://dx.doi.org/10.1073/pnas.2101918118
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