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Cross-protective antibodies against common endemic respiratory viruses
Respiratory syncytial virus (RSV), human metapneumovirus (HMPV), and human parainfluenza virus types one (HPIV1) and three (HPIV3) can cause severe disease and death in immunocompromised patients, the elderly, and those with underlying lung disease. A protective monoclonal antibody exists for RSV, b...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9923667/ https://www.ncbi.nlm.nih.gov/pubmed/36781872 http://dx.doi.org/10.1038/s41467-023-36459-3 |
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author | Cabán, Madelyn Rodarte, Justas V. Bibby, Madeleine Gray, Matthew D. Taylor, Justin J. Pancera, Marie Boonyaratanakornkit, Jim |
author_facet | Cabán, Madelyn Rodarte, Justas V. Bibby, Madeleine Gray, Matthew D. Taylor, Justin J. Pancera, Marie Boonyaratanakornkit, Jim |
author_sort | Cabán, Madelyn |
collection | PubMed |
description | Respiratory syncytial virus (RSV), human metapneumovirus (HMPV), and human parainfluenza virus types one (HPIV1) and three (HPIV3) can cause severe disease and death in immunocompromised patients, the elderly, and those with underlying lung disease. A protective monoclonal antibody exists for RSV, but clinical use is limited to high-risk infant populations. Hence, therapeutic options for these viruses in vulnerable patient populations are currently limited. Here, we present the discovery, in vitro characterization, and in vivo efficacy testing of two cross-neutralizing monoclonal antibodies, one targeting both HPIV3 and HPIV1 and the other targeting both RSV and HMPV. The 3 × 1 antibody is capable of targeting multiple parainfluenza viruses; the MxR antibody shares features with other previously reported monoclonal antibodies that are capable of neutralizing both RSV and HMPV. We obtained structures using cryo-electron microscopy of these antibodies in complex with their antigens at 3.62 Å resolution for 3 × 1 bound to HPIV3 and at 2.24 Å for MxR bound to RSV, providing a structural basis for in vitro binding and neutralization. Together, a cocktail of 3 × 1 and MxR could have clinical utility in providing broad protection against four of the respiratory viruses that cause significant morbidity and mortality in at-risk individuals. |
format | Online Article Text |
id | pubmed-9923667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99236672023-02-13 Cross-protective antibodies against common endemic respiratory viruses Cabán, Madelyn Rodarte, Justas V. Bibby, Madeleine Gray, Matthew D. Taylor, Justin J. Pancera, Marie Boonyaratanakornkit, Jim Nat Commun Article Respiratory syncytial virus (RSV), human metapneumovirus (HMPV), and human parainfluenza virus types one (HPIV1) and three (HPIV3) can cause severe disease and death in immunocompromised patients, the elderly, and those with underlying lung disease. A protective monoclonal antibody exists for RSV, but clinical use is limited to high-risk infant populations. Hence, therapeutic options for these viruses in vulnerable patient populations are currently limited. Here, we present the discovery, in vitro characterization, and in vivo efficacy testing of two cross-neutralizing monoclonal antibodies, one targeting both HPIV3 and HPIV1 and the other targeting both RSV and HMPV. The 3 × 1 antibody is capable of targeting multiple parainfluenza viruses; the MxR antibody shares features with other previously reported monoclonal antibodies that are capable of neutralizing both RSV and HMPV. We obtained structures using cryo-electron microscopy of these antibodies in complex with their antigens at 3.62 Å resolution for 3 × 1 bound to HPIV3 and at 2.24 Å for MxR bound to RSV, providing a structural basis for in vitro binding and neutralization. Together, a cocktail of 3 × 1 and MxR could have clinical utility in providing broad protection against four of the respiratory viruses that cause significant morbidity and mortality in at-risk individuals. Nature Publishing Group UK 2023-02-13 /pmc/articles/PMC9923667/ /pubmed/36781872 http://dx.doi.org/10.1038/s41467-023-36459-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Cabán, Madelyn Rodarte, Justas V. Bibby, Madeleine Gray, Matthew D. Taylor, Justin J. Pancera, Marie Boonyaratanakornkit, Jim Cross-protective antibodies against common endemic respiratory viruses |
title | Cross-protective antibodies against common endemic respiratory viruses |
title_full | Cross-protective antibodies against common endemic respiratory viruses |
title_fullStr | Cross-protective antibodies against common endemic respiratory viruses |
title_full_unstemmed | Cross-protective antibodies against common endemic respiratory viruses |
title_short | Cross-protective antibodies against common endemic respiratory viruses |
title_sort | cross-protective antibodies against common endemic respiratory viruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9923667/ https://www.ncbi.nlm.nih.gov/pubmed/36781872 http://dx.doi.org/10.1038/s41467-023-36459-3 |
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