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SARS-CoV-2 neutralizing antibody bebtelovimab – a systematic scoping review and meta-analysis
INTRODUCTION: The COVID-19 pandemic is a major global public health crisis. More than 2 years into the pandemic, effective therapeutic options remain limited due to rapid viral evolution. Stemming from the emergence of multiple variants, several monoclonal antibodies are no longer suitable for clini...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10494534/ https://www.ncbi.nlm.nih.gov/pubmed/37701439 http://dx.doi.org/10.3389/fimmu.2023.1100263 |
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author | Liew, Mabel Nyit Yi Kua, Kok Pim Lee, Shaun Wen Huey Wong, Kon Ken |
author_facet | Liew, Mabel Nyit Yi Kua, Kok Pim Lee, Shaun Wen Huey Wong, Kon Ken |
author_sort | Liew, Mabel Nyit Yi |
collection | PubMed |
description | INTRODUCTION: The COVID-19 pandemic is a major global public health crisis. More than 2 years into the pandemic, effective therapeutic options remain limited due to rapid viral evolution. Stemming from the emergence of multiple variants, several monoclonal antibodies are no longer suitable for clinical use. This scoping review aimed to summarize the preclinical and clinical evidence for bebtelovimab in treating newly emerging SARS-CoV-2 variants. METHODS: We systematically searched five electronic databases (PubMed, CENTRAL, Embase, Global Health, and PsycINFO) from date of inception to September 30, 2022, for studies reporting on the effect of bebtelovimab in SARS-CoV-2 infection, using a combination of search terms around ―bebtelovimab‖, ―LY-CoV1404‖, ―LY3853113‖, and ―coronavirus infection‖. All citations were screened independently by two researchers. Data were extracted and thematically analyzed based on study design by adhering to the stipulated scoping review approaches. RESULTS: Thirty-nine studies were included, thirty-four non-clinical studies were narratively synthesized, and five clinical studies were meta-analyzed. The non-clinical studies revealed bebtelovimab not only potently neutralized wide-type SARS-CoV-2 and existing variants of concern such as B.1.1.7 (Alpha), B.1.351 (Beta), P.1 (Gamma), and B.1.617.2 (Delta), but also retained appreciable activity against Omicron lineages, including BA.2.75, BA.4, BA.4.6, and BA.5. Unlike other monoclonal antibodies, bebtelovimab was able to bind to epitope of the SARS-CoV-2 S protein by exploiting loop mobility or by minimizing side-chain interactions. Pooled analysis from clinical studies depicted that the rates of hospitalization, ICU admission, and death were similar between bebtelovimab and other COVID-19 therapies. Bebtelovimab was associated with a low incidence of treatment-emergent adverse events. CONCLUSION: Preclinical evidence suggests bebtelovimab be a potential treatment for COVID-19 amidst viral evolution. Bebtelovimab has comparable efficacy to other COVID-19 therapies without evident safety concerns. |
format | Online Article Text |
id | pubmed-10494534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104945342023-09-12 SARS-CoV-2 neutralizing antibody bebtelovimab – a systematic scoping review and meta-analysis Liew, Mabel Nyit Yi Kua, Kok Pim Lee, Shaun Wen Huey Wong, Kon Ken Front Immunol Immunology INTRODUCTION: The COVID-19 pandemic is a major global public health crisis. More than 2 years into the pandemic, effective therapeutic options remain limited due to rapid viral evolution. Stemming from the emergence of multiple variants, several monoclonal antibodies are no longer suitable for clinical use. This scoping review aimed to summarize the preclinical and clinical evidence for bebtelovimab in treating newly emerging SARS-CoV-2 variants. METHODS: We systematically searched five electronic databases (PubMed, CENTRAL, Embase, Global Health, and PsycINFO) from date of inception to September 30, 2022, for studies reporting on the effect of bebtelovimab in SARS-CoV-2 infection, using a combination of search terms around ―bebtelovimab‖, ―LY-CoV1404‖, ―LY3853113‖, and ―coronavirus infection‖. All citations were screened independently by two researchers. Data were extracted and thematically analyzed based on study design by adhering to the stipulated scoping review approaches. RESULTS: Thirty-nine studies were included, thirty-four non-clinical studies were narratively synthesized, and five clinical studies were meta-analyzed. The non-clinical studies revealed bebtelovimab not only potently neutralized wide-type SARS-CoV-2 and existing variants of concern such as B.1.1.7 (Alpha), B.1.351 (Beta), P.1 (Gamma), and B.1.617.2 (Delta), but also retained appreciable activity against Omicron lineages, including BA.2.75, BA.4, BA.4.6, and BA.5. Unlike other monoclonal antibodies, bebtelovimab was able to bind to epitope of the SARS-CoV-2 S protein by exploiting loop mobility or by minimizing side-chain interactions. Pooled analysis from clinical studies depicted that the rates of hospitalization, ICU admission, and death were similar between bebtelovimab and other COVID-19 therapies. Bebtelovimab was associated with a low incidence of treatment-emergent adverse events. CONCLUSION: Preclinical evidence suggests bebtelovimab be a potential treatment for COVID-19 amidst viral evolution. Bebtelovimab has comparable efficacy to other COVID-19 therapies without evident safety concerns. Frontiers Media S.A. 2023-08-28 /pmc/articles/PMC10494534/ /pubmed/37701439 http://dx.doi.org/10.3389/fimmu.2023.1100263 Text en Copyright © 2023 Liew, Kua, Lee and Wong https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Liew, Mabel Nyit Yi Kua, Kok Pim Lee, Shaun Wen Huey Wong, Kon Ken SARS-CoV-2 neutralizing antibody bebtelovimab – a systematic scoping review and meta-analysis |
title | SARS-CoV-2 neutralizing antibody bebtelovimab – a systematic scoping review and meta-analysis |
title_full | SARS-CoV-2 neutralizing antibody bebtelovimab – a systematic scoping review and meta-analysis |
title_fullStr | SARS-CoV-2 neutralizing antibody bebtelovimab – a systematic scoping review and meta-analysis |
title_full_unstemmed | SARS-CoV-2 neutralizing antibody bebtelovimab – a systematic scoping review and meta-analysis |
title_short | SARS-CoV-2 neutralizing antibody bebtelovimab – a systematic scoping review and meta-analysis |
title_sort | sars-cov-2 neutralizing antibody bebtelovimab – a systematic scoping review and meta-analysis |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10494534/ https://www.ncbi.nlm.nih.gov/pubmed/37701439 http://dx.doi.org/10.3389/fimmu.2023.1100263 |
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