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Ebanga™: The most recent FDA-approved drug for treating Ebola
Ebolavirus (EBOV) is a virulent pathogen that causes Ebola virus disease (EVD), which is a life-threatening human condition with a fatality rate of up to 90%. Since the first outbreak in Africa in 1976, several outbreaks and epidemics of EBOV have occurred across the globe. While EVD is recognized a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032372/ https://www.ncbi.nlm.nih.gov/pubmed/36969842 http://dx.doi.org/10.3389/fphar.2023.1083429 |
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author | Taki, Elahe Ghanavati, Roya Navidifar, Tahereh Dashtbin, Shirin Heidary, Mohsen Moghadamnia, Marjan |
author_facet | Taki, Elahe Ghanavati, Roya Navidifar, Tahereh Dashtbin, Shirin Heidary, Mohsen Moghadamnia, Marjan |
author_sort | Taki, Elahe |
collection | PubMed |
description | Ebolavirus (EBOV) is a virulent pathogen that causes Ebola virus disease (EVD), which is a life-threatening human condition with a fatality rate of up to 90%. Since the first outbreak in Africa in 1976, several outbreaks and epidemics of EBOV have occurred across the globe. While EVD is recognized as a serious threat to human health and outbreaks occur almost every year, the treatment options for the disease are limited. In designing therapeutic strategies against EBOV infection, viral structural proteins, such as glycoprotein (GP), could be an excellent target for neutralizing the virus. According to the latest research, GP-specific antibodies are the most efficient post-exposure treatments for EVD. Ansuvimab-zykl, i.e., mAb114 (Ebanga™), is a recent FDA-approved human immunoglobulin monoclonal antibody targeting EBOV GP. This review provides a brief overview of the pharmacological effects and safety profile of ansuvimab in clinical trials and provides insights into the precise mechanism of this new drug for treating EVD. |
format | Online Article Text |
id | pubmed-10032372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100323722023-03-23 Ebanga™: The most recent FDA-approved drug for treating Ebola Taki, Elahe Ghanavati, Roya Navidifar, Tahereh Dashtbin, Shirin Heidary, Mohsen Moghadamnia, Marjan Front Pharmacol Pharmacology Ebolavirus (EBOV) is a virulent pathogen that causes Ebola virus disease (EVD), which is a life-threatening human condition with a fatality rate of up to 90%. Since the first outbreak in Africa in 1976, several outbreaks and epidemics of EBOV have occurred across the globe. While EVD is recognized as a serious threat to human health and outbreaks occur almost every year, the treatment options for the disease are limited. In designing therapeutic strategies against EBOV infection, viral structural proteins, such as glycoprotein (GP), could be an excellent target for neutralizing the virus. According to the latest research, GP-specific antibodies are the most efficient post-exposure treatments for EVD. Ansuvimab-zykl, i.e., mAb114 (Ebanga™), is a recent FDA-approved human immunoglobulin monoclonal antibody targeting EBOV GP. This review provides a brief overview of the pharmacological effects and safety profile of ansuvimab in clinical trials and provides insights into the precise mechanism of this new drug for treating EVD. Frontiers Media S.A. 2023-03-08 /pmc/articles/PMC10032372/ /pubmed/36969842 http://dx.doi.org/10.3389/fphar.2023.1083429 Text en Copyright © 2023 Taki, Ghanavati, Navidifar, Dashtbin, Heidary and Moghadamnia. 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 | Pharmacology Taki, Elahe Ghanavati, Roya Navidifar, Tahereh Dashtbin, Shirin Heidary, Mohsen Moghadamnia, Marjan Ebanga™: The most recent FDA-approved drug for treating Ebola |
title | Ebanga™: The most recent FDA-approved drug for treating Ebola |
title_full | Ebanga™: The most recent FDA-approved drug for treating Ebola |
title_fullStr | Ebanga™: The most recent FDA-approved drug for treating Ebola |
title_full_unstemmed | Ebanga™: The most recent FDA-approved drug for treating Ebola |
title_short | Ebanga™: The most recent FDA-approved drug for treating Ebola |
title_sort | ebanga™: the most recent fda-approved drug for treating ebola |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032372/ https://www.ncbi.nlm.nih.gov/pubmed/36969842 http://dx.doi.org/10.3389/fphar.2023.1083429 |
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