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Efficacy of COVID-HIGIV in animal models of SARS-CoV-2 infection
In late 2019 the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus emerged in China and quickly spread into a worldwide pandemic. It has caused millions of hospitalizations and deaths, despite the use of COVID-19 vaccines. Convalescent plasma and monoclonal antibodies emerged as maj...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549041/ https://www.ncbi.nlm.nih.gov/pubmed/36216961 http://dx.doi.org/10.1038/s41598-022-21223-2 |
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author | Jha, Aruni Barker, Douglas Lew, Jocelyne Manoharan, Vinoth van Kessel, Jill Haupt, Robert Toth, Derek Frieman, Matthew Falzarano, Darryl Kodihalli, Shantha |
author_facet | Jha, Aruni Barker, Douglas Lew, Jocelyne Manoharan, Vinoth van Kessel, Jill Haupt, Robert Toth, Derek Frieman, Matthew Falzarano, Darryl Kodihalli, Shantha |
author_sort | Jha, Aruni |
collection | PubMed |
description | In late 2019 the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus emerged in China and quickly spread into a worldwide pandemic. It has caused millions of hospitalizations and deaths, despite the use of COVID-19 vaccines. Convalescent plasma and monoclonal antibodies emerged as major therapeutic options for treatment of COVID-19. We have developed an anti-SARS-CoV-2 immunoglobulin intravenous (Human) (COVID-HIGIV), a potential improvement from using convalescent plasma. In this report the efficacy of COVID-HIGIV was evaluated in hamster and mouse models of SARS-CoV-2 infection. COVID-HIGIV treatment in both mice and hamsters significantly reduced the viral load in the lungs. Among COVID-HIGIV treated animals, infection-related body weight loss was reduced and the animals regained their baseline body weight faster than the PBS controls. In hamsters, COVID-HIGIV treatment reduced infection-associated lung pathology including lung inflammation, and pneumocyte hypertrophy in the lungs. These results support ongoing trials for outpatient treatment with COVID-HIGIV for safety and efficacy evaluation (NCT04910269, NCT04546581). |
format | Online Article Text |
id | pubmed-9549041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95490412022-10-11 Efficacy of COVID-HIGIV in animal models of SARS-CoV-2 infection Jha, Aruni Barker, Douglas Lew, Jocelyne Manoharan, Vinoth van Kessel, Jill Haupt, Robert Toth, Derek Frieman, Matthew Falzarano, Darryl Kodihalli, Shantha Sci Rep Article In late 2019 the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus emerged in China and quickly spread into a worldwide pandemic. It has caused millions of hospitalizations and deaths, despite the use of COVID-19 vaccines. Convalescent plasma and monoclonal antibodies emerged as major therapeutic options for treatment of COVID-19. We have developed an anti-SARS-CoV-2 immunoglobulin intravenous (Human) (COVID-HIGIV), a potential improvement from using convalescent plasma. In this report the efficacy of COVID-HIGIV was evaluated in hamster and mouse models of SARS-CoV-2 infection. COVID-HIGIV treatment in both mice and hamsters significantly reduced the viral load in the lungs. Among COVID-HIGIV treated animals, infection-related body weight loss was reduced and the animals regained their baseline body weight faster than the PBS controls. In hamsters, COVID-HIGIV treatment reduced infection-associated lung pathology including lung inflammation, and pneumocyte hypertrophy in the lungs. These results support ongoing trials for outpatient treatment with COVID-HIGIV for safety and efficacy evaluation (NCT04910269, NCT04546581). Nature Publishing Group UK 2022-10-10 /pmc/articles/PMC9549041/ /pubmed/36216961 http://dx.doi.org/10.1038/s41598-022-21223-2 Text en © The Author(s) 2022 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jha, Aruni Barker, Douglas Lew, Jocelyne Manoharan, Vinoth van Kessel, Jill Haupt, Robert Toth, Derek Frieman, Matthew Falzarano, Darryl Kodihalli, Shantha Efficacy of COVID-HIGIV in animal models of SARS-CoV-2 infection |
title | Efficacy of COVID-HIGIV in animal models of SARS-CoV-2 infection |
title_full | Efficacy of COVID-HIGIV in animal models of SARS-CoV-2 infection |
title_fullStr | Efficacy of COVID-HIGIV in animal models of SARS-CoV-2 infection |
title_full_unstemmed | Efficacy of COVID-HIGIV in animal models of SARS-CoV-2 infection |
title_short | Efficacy of COVID-HIGIV in animal models of SARS-CoV-2 infection |
title_sort | efficacy of covid-higiv in animal models of sars-cov-2 infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549041/ https://www.ncbi.nlm.nih.gov/pubmed/36216961 http://dx.doi.org/10.1038/s41598-022-21223-2 |
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