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Human neutralizing antibodies for SARS-CoV-2 prevention and immunotherapy
Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is the causative agent of coronavirus disease 2019 (COVID-19). SARS-CoV-2 has been spreading worldwide since December 2019, resulting in the ongoing COVID-19 pandemic with 237 million infections and 4.8 million deaths by 11 October 2021. W...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755319/ https://www.ncbi.nlm.nih.gov/pubmed/35915816 http://dx.doi.org/10.1093/immadv/ltab027 |
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author | Zhou, Dongyan Zhou, Runhong Chen, Zhiwei |
author_facet | Zhou, Dongyan Zhou, Runhong Chen, Zhiwei |
author_sort | Zhou, Dongyan |
collection | PubMed |
description | Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is the causative agent of coronavirus disease 2019 (COVID-19). SARS-CoV-2 has been spreading worldwide since December 2019, resulting in the ongoing COVID-19 pandemic with 237 million infections and 4.8 million deaths by 11 October 2021. While there are great efforts of global vaccination, ending this pandemic has been challenged by issues of exceptionally high viral transmissibility, re-infection, vaccine-breakthrough infection, and immune escape variants of concern. Besides the record-breaking speed of vaccine research and development, antiviral drugs including SARS-CoV-2-specific human neutralizing antibodies (HuNAbs) have been actively explored for passive immunization. In support of HuNAb-based immunotherapy, passive immunization using convalescent patients’ plasma has generated promising evidence on clinical benefits for both mild and severe COVID-19 patients. Since the source of convalescent plasma is limited, the discovery of broadly reactive HuNAbs may have significant impacts on the fight against the COVID-19 pandemic. In this review, therefore, we discuss the current technologies of gene cloning, modes of action, in vitro and in vivo potency and breadth, and clinical development for potent SARS-CoV-2-specific HuNAbs. |
format | Online Article Text |
id | pubmed-8755319 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-87553192022-01-13 Human neutralizing antibodies for SARS-CoV-2 prevention and immunotherapy Zhou, Dongyan Zhou, Runhong Chen, Zhiwei Immunother Adv Adoptive Cellular Immunotherapies Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is the causative agent of coronavirus disease 2019 (COVID-19). SARS-CoV-2 has been spreading worldwide since December 2019, resulting in the ongoing COVID-19 pandemic with 237 million infections and 4.8 million deaths by 11 October 2021. While there are great efforts of global vaccination, ending this pandemic has been challenged by issues of exceptionally high viral transmissibility, re-infection, vaccine-breakthrough infection, and immune escape variants of concern. Besides the record-breaking speed of vaccine research and development, antiviral drugs including SARS-CoV-2-specific human neutralizing antibodies (HuNAbs) have been actively explored for passive immunization. In support of HuNAb-based immunotherapy, passive immunization using convalescent patients’ plasma has generated promising evidence on clinical benefits for both mild and severe COVID-19 patients. Since the source of convalescent plasma is limited, the discovery of broadly reactive HuNAbs may have significant impacts on the fight against the COVID-19 pandemic. In this review, therefore, we discuss the current technologies of gene cloning, modes of action, in vitro and in vivo potency and breadth, and clinical development for potent SARS-CoV-2-specific HuNAbs. Oxford University Press 2021-12-30 /pmc/articles/PMC8755319/ /pubmed/35915816 http://dx.doi.org/10.1093/immadv/ltab027 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Immunology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Adoptive Cellular Immunotherapies Zhou, Dongyan Zhou, Runhong Chen, Zhiwei Human neutralizing antibodies for SARS-CoV-2 prevention and immunotherapy |
title | Human neutralizing antibodies for SARS-CoV-2 prevention and immunotherapy |
title_full | Human neutralizing antibodies for SARS-CoV-2 prevention and immunotherapy |
title_fullStr | Human neutralizing antibodies for SARS-CoV-2 prevention and immunotherapy |
title_full_unstemmed | Human neutralizing antibodies for SARS-CoV-2 prevention and immunotherapy |
title_short | Human neutralizing antibodies for SARS-CoV-2 prevention and immunotherapy |
title_sort | human neutralizing antibodies for sars-cov-2 prevention and immunotherapy |
topic | Adoptive Cellular Immunotherapies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755319/ https://www.ncbi.nlm.nih.gov/pubmed/35915816 http://dx.doi.org/10.1093/immadv/ltab027 |
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