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Development of a Well-Characterized Cynomolgus Macaque Model of Marburg Virus Disease for Support of Vaccine and Therapy Development
Marburg virus (MARV) is a filovirus that can infect humans and nonhuman primates (NHPs), causing severe disease and death. Of the filoviruses, Ebola virus (EBOV) has been the primary target for vaccine and therapeutic development. However, MARV has an average case fatality rate of approximately 50%,...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9414819/ https://www.ncbi.nlm.nih.gov/pubmed/36016203 http://dx.doi.org/10.3390/vaccines10081314 |
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author | Alfson, Kendra J. Goez-Gazi, Yenny Gazi, Michal Chou, Ying-Liang Niemuth, Nancy A. Mattix, Marc E. Staples, Hilary M. Klaffke, Benjamin Rodriguez, Gloria F. Bartley, Carmen Ticer, Anysha Clemmons, Elizabeth A. Dutton, John W. Griffiths, Anthony Meister, Gabe T. Sanford, Daniel C. Cirimotich, Chris M. Carrion, Ricardo |
author_facet | Alfson, Kendra J. Goez-Gazi, Yenny Gazi, Michal Chou, Ying-Liang Niemuth, Nancy A. Mattix, Marc E. Staples, Hilary M. Klaffke, Benjamin Rodriguez, Gloria F. Bartley, Carmen Ticer, Anysha Clemmons, Elizabeth A. Dutton, John W. Griffiths, Anthony Meister, Gabe T. Sanford, Daniel C. Cirimotich, Chris M. Carrion, Ricardo |
author_sort | Alfson, Kendra J. |
collection | PubMed |
description | Marburg virus (MARV) is a filovirus that can infect humans and nonhuman primates (NHPs), causing severe disease and death. Of the filoviruses, Ebola virus (EBOV) has been the primary target for vaccine and therapeutic development. However, MARV has an average case fatality rate of approximately 50%, the infectious dose is low, and there are currently no approved vaccines or therapies targeted at infection with MARV. The purpose of this study was to characterize disease course in cynomolgus macaques intramuscularly exposed to MARV Angola variant. There were several biomarkers that reliably correlated with MARV-induced disease, including: viral load; elevated total clinical scores; temperature changes; elevated ALT, ALP, BA, TBIL, CRP and decreased ALB values; decreased lymphocytes and platelets; and prolonged PTT. A scheduled euthanasia component also provided the opportunity to study the earliest stages of the disease. This study provides evidence for the application of this model to evaluate potential vaccines and therapies against MARV and will be valuable in improving existing models. |
format | Online Article Text |
id | pubmed-9414819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94148192022-08-27 Development of a Well-Characterized Cynomolgus Macaque Model of Marburg Virus Disease for Support of Vaccine and Therapy Development Alfson, Kendra J. Goez-Gazi, Yenny Gazi, Michal Chou, Ying-Liang Niemuth, Nancy A. Mattix, Marc E. Staples, Hilary M. Klaffke, Benjamin Rodriguez, Gloria F. Bartley, Carmen Ticer, Anysha Clemmons, Elizabeth A. Dutton, John W. Griffiths, Anthony Meister, Gabe T. Sanford, Daniel C. Cirimotich, Chris M. Carrion, Ricardo Vaccines (Basel) Article Marburg virus (MARV) is a filovirus that can infect humans and nonhuman primates (NHPs), causing severe disease and death. Of the filoviruses, Ebola virus (EBOV) has been the primary target for vaccine and therapeutic development. However, MARV has an average case fatality rate of approximately 50%, the infectious dose is low, and there are currently no approved vaccines or therapies targeted at infection with MARV. The purpose of this study was to characterize disease course in cynomolgus macaques intramuscularly exposed to MARV Angola variant. There were several biomarkers that reliably correlated with MARV-induced disease, including: viral load; elevated total clinical scores; temperature changes; elevated ALT, ALP, BA, TBIL, CRP and decreased ALB values; decreased lymphocytes and platelets; and prolonged PTT. A scheduled euthanasia component also provided the opportunity to study the earliest stages of the disease. This study provides evidence for the application of this model to evaluate potential vaccines and therapies against MARV and will be valuable in improving existing models. MDPI 2022-08-14 /pmc/articles/PMC9414819/ /pubmed/36016203 http://dx.doi.org/10.3390/vaccines10081314 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Alfson, Kendra J. Goez-Gazi, Yenny Gazi, Michal Chou, Ying-Liang Niemuth, Nancy A. Mattix, Marc E. Staples, Hilary M. Klaffke, Benjamin Rodriguez, Gloria F. Bartley, Carmen Ticer, Anysha Clemmons, Elizabeth A. Dutton, John W. Griffiths, Anthony Meister, Gabe T. Sanford, Daniel C. Cirimotich, Chris M. Carrion, Ricardo Development of a Well-Characterized Cynomolgus Macaque Model of Marburg Virus Disease for Support of Vaccine and Therapy Development |
title | Development of a Well-Characterized Cynomolgus Macaque Model of Marburg Virus Disease for Support of Vaccine and Therapy Development |
title_full | Development of a Well-Characterized Cynomolgus Macaque Model of Marburg Virus Disease for Support of Vaccine and Therapy Development |
title_fullStr | Development of a Well-Characterized Cynomolgus Macaque Model of Marburg Virus Disease for Support of Vaccine and Therapy Development |
title_full_unstemmed | Development of a Well-Characterized Cynomolgus Macaque Model of Marburg Virus Disease for Support of Vaccine and Therapy Development |
title_short | Development of a Well-Characterized Cynomolgus Macaque Model of Marburg Virus Disease for Support of Vaccine and Therapy Development |
title_sort | development of a well-characterized cynomolgus macaque model of marburg virus disease for support of vaccine and therapy development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9414819/ https://www.ncbi.nlm.nih.gov/pubmed/36016203 http://dx.doi.org/10.3390/vaccines10081314 |
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