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Improved control of SARS-CoV-2 by treatment with a nucleocapsid-specific monoclonal antibody

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein is the main antigen in all approved COVID-19 vaccines and is also the only target for monoclonal antibody (mAb) therapies. Immune responses to other viral antigens are generated after SARS-CoV-2 infection, but their contr...

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Autores principales: Dangi, Tanushree, Sanchez, Sarah, Class, Jacob, Richner, Michelle, Visvabharathy, Lavanya, Chung, Young Rock, Bentley, Kirsten, Stanton, Richard J., Koralnik, Igor J., Richner, Justin M., Penaloza-MacMaster, Pablo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Clinical Investigation 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9711872/
https://www.ncbi.nlm.nih.gov/pubmed/36219482
http://dx.doi.org/10.1172/JCI162282
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author Dangi, Tanushree
Sanchez, Sarah
Class, Jacob
Richner, Michelle
Visvabharathy, Lavanya
Chung, Young Rock
Bentley, Kirsten
Stanton, Richard J.
Koralnik, Igor J.
Richner, Justin M.
Penaloza-MacMaster, Pablo
author_facet Dangi, Tanushree
Sanchez, Sarah
Class, Jacob
Richner, Michelle
Visvabharathy, Lavanya
Chung, Young Rock
Bentley, Kirsten
Stanton, Richard J.
Koralnik, Igor J.
Richner, Justin M.
Penaloza-MacMaster, Pablo
author_sort Dangi, Tanushree
collection PubMed
description The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein is the main antigen in all approved COVID-19 vaccines and is also the only target for monoclonal antibody (mAb) therapies. Immune responses to other viral antigens are generated after SARS-CoV-2 infection, but their contribution to the antiviral response remains unclear. Here, we interrogated whether nucleocapsid-specific antibodies can improve protection against SARS-CoV-2. We first immunized mice with a nucleocapsid-based vaccine and then transferred sera from these mice into naive mice, followed by challenge with SARS-CoV-2. We show that mice that received nucleocapsid-specific sera or a nucleocapsid-specific mAb exhibited enhanced control of SARS-CoV-2. Nucleocapsid-specific antibodies elicited NK-mediated, antibody-dependent cellular cytotoxicity (ADCC) against infected cells. To our knowledge, these findings provide the first demonstration in the coronavirus literature that antibody responses specific to the nucleocapsid protein can improve viral clearance, providing a rationale for the clinical evaluation of nucleocapsid-based mAb therapies to treat COVID-19.
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spelling pubmed-97118722022-12-05 Improved control of SARS-CoV-2 by treatment with a nucleocapsid-specific monoclonal antibody Dangi, Tanushree Sanchez, Sarah Class, Jacob Richner, Michelle Visvabharathy, Lavanya Chung, Young Rock Bentley, Kirsten Stanton, Richard J. Koralnik, Igor J. Richner, Justin M. Penaloza-MacMaster, Pablo J Clin Invest Research Article The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein is the main antigen in all approved COVID-19 vaccines and is also the only target for monoclonal antibody (mAb) therapies. Immune responses to other viral antigens are generated after SARS-CoV-2 infection, but their contribution to the antiviral response remains unclear. Here, we interrogated whether nucleocapsid-specific antibodies can improve protection against SARS-CoV-2. We first immunized mice with a nucleocapsid-based vaccine and then transferred sera from these mice into naive mice, followed by challenge with SARS-CoV-2. We show that mice that received nucleocapsid-specific sera or a nucleocapsid-specific mAb exhibited enhanced control of SARS-CoV-2. Nucleocapsid-specific antibodies elicited NK-mediated, antibody-dependent cellular cytotoxicity (ADCC) against infected cells. To our knowledge, these findings provide the first demonstration in the coronavirus literature that antibody responses specific to the nucleocapsid protein can improve viral clearance, providing a rationale for the clinical evaluation of nucleocapsid-based mAb therapies to treat COVID-19. American Society for Clinical Investigation 2022-12-01 /pmc/articles/PMC9711872/ /pubmed/36219482 http://dx.doi.org/10.1172/JCI162282 Text en © 2022 Dangi et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Dangi, Tanushree
Sanchez, Sarah
Class, Jacob
Richner, Michelle
Visvabharathy, Lavanya
Chung, Young Rock
Bentley, Kirsten
Stanton, Richard J.
Koralnik, Igor J.
Richner, Justin M.
Penaloza-MacMaster, Pablo
Improved control of SARS-CoV-2 by treatment with a nucleocapsid-specific monoclonal antibody
title Improved control of SARS-CoV-2 by treatment with a nucleocapsid-specific monoclonal antibody
title_full Improved control of SARS-CoV-2 by treatment with a nucleocapsid-specific monoclonal antibody
title_fullStr Improved control of SARS-CoV-2 by treatment with a nucleocapsid-specific monoclonal antibody
title_full_unstemmed Improved control of SARS-CoV-2 by treatment with a nucleocapsid-specific monoclonal antibody
title_short Improved control of SARS-CoV-2 by treatment with a nucleocapsid-specific monoclonal antibody
title_sort improved control of sars-cov-2 by treatment with a nucleocapsid-specific monoclonal antibody
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9711872/
https://www.ncbi.nlm.nih.gov/pubmed/36219482
http://dx.doi.org/10.1172/JCI162282
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