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New Developments and Challenges in Antibody-Based Therapies for the Respiratory Syncytial Virus
Since the discovery of the human respiratory syncytial virus (hRSV), multiple research efforts have been conducted to develop vaccines and treatments capable of reducing the risk of severe disease, hospitalization, long-term sequelae, and death from this pathogen in susceptible populations. In this...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10094422/ https://www.ncbi.nlm.nih.gov/pubmed/37063935 http://dx.doi.org/10.2147/IDR.S379660 |
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author | Diethelm-Varela, Benjamín Soto, Jorge A Riedel, Claudia A Bueno, Susan M Kalergis, Alexis M |
author_facet | Diethelm-Varela, Benjamín Soto, Jorge A Riedel, Claudia A Bueno, Susan M Kalergis, Alexis M |
author_sort | Diethelm-Varela, Benjamín |
collection | PubMed |
description | Since the discovery of the human respiratory syncytial virus (hRSV), multiple research efforts have been conducted to develop vaccines and treatments capable of reducing the risk of severe disease, hospitalization, long-term sequelae, and death from this pathogen in susceptible populations. In this sense, therapies specifically directed against hRSV are mainly based on monoclonal and polyclonal antibodies such as intravenous IgG (IVIG)-RSV and the monoclonal antibody palivizumab. However, these therapies are associated with significant limitations, including the need for the recruitment of a high number of convalescent volunteers who donate blood to procure IVIG-RSV and the costs associated with the need for repeated administrations of palivizumab. These limitations render this product not cost-effective for populations other than high-risk patients. These problems have underscored that it is still necessary to identify new safe and effective therapies for human use. However, these new therapies must benefit from a comparatively cheap production cost and the opportunity to be available to the high-risk population and anyone who requires treatment. Here, we review the different antibodies used to prevent the pathology caused by hRSV infection, highlighting therapies currently approved for human use and their clinical value. Also, the new, most promising candidates based on preclinical studies and clinical trial results are revised. |
format | Online Article Text |
id | pubmed-10094422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-100944222023-04-13 New Developments and Challenges in Antibody-Based Therapies for the Respiratory Syncytial Virus Diethelm-Varela, Benjamín Soto, Jorge A Riedel, Claudia A Bueno, Susan M Kalergis, Alexis M Infect Drug Resist Review Since the discovery of the human respiratory syncytial virus (hRSV), multiple research efforts have been conducted to develop vaccines and treatments capable of reducing the risk of severe disease, hospitalization, long-term sequelae, and death from this pathogen in susceptible populations. In this sense, therapies specifically directed against hRSV are mainly based on monoclonal and polyclonal antibodies such as intravenous IgG (IVIG)-RSV and the monoclonal antibody palivizumab. However, these therapies are associated with significant limitations, including the need for the recruitment of a high number of convalescent volunteers who donate blood to procure IVIG-RSV and the costs associated with the need for repeated administrations of palivizumab. These limitations render this product not cost-effective for populations other than high-risk patients. These problems have underscored that it is still necessary to identify new safe and effective therapies for human use. However, these new therapies must benefit from a comparatively cheap production cost and the opportunity to be available to the high-risk population and anyone who requires treatment. Here, we review the different antibodies used to prevent the pathology caused by hRSV infection, highlighting therapies currently approved for human use and their clinical value. Also, the new, most promising candidates based on preclinical studies and clinical trial results are revised. Dove 2023-04-08 /pmc/articles/PMC10094422/ /pubmed/37063935 http://dx.doi.org/10.2147/IDR.S379660 Text en © 2023 Diethelm-Varela et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Review Diethelm-Varela, Benjamín Soto, Jorge A Riedel, Claudia A Bueno, Susan M Kalergis, Alexis M New Developments and Challenges in Antibody-Based Therapies for the Respiratory Syncytial Virus |
title | New Developments and Challenges in Antibody-Based Therapies for the Respiratory Syncytial Virus |
title_full | New Developments and Challenges in Antibody-Based Therapies for the Respiratory Syncytial Virus |
title_fullStr | New Developments and Challenges in Antibody-Based Therapies for the Respiratory Syncytial Virus |
title_full_unstemmed | New Developments and Challenges in Antibody-Based Therapies for the Respiratory Syncytial Virus |
title_short | New Developments and Challenges in Antibody-Based Therapies for the Respiratory Syncytial Virus |
title_sort | new developments and challenges in antibody-based therapies for the respiratory syncytial virus |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10094422/ https://www.ncbi.nlm.nih.gov/pubmed/37063935 http://dx.doi.org/10.2147/IDR.S379660 |
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