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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2022
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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. |
format | Online Article Text |
id | pubmed-9711872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
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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