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Post-exposure treatment of Ebola virus disease in guinea pigs using EBOTAb, an ovine antibody-based therapeutic
Ebola virus (EBOV) is highly pathogenic, with a predisposition to cause outbreaks in human populations accompanied by significant mortality. An ovine polyclonal antibody therapy has been developed against EBOV, named EBOTAb. When tested in the stringent guinea pig model of EBOV disease, EBOTAb has b...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964638/ https://www.ncbi.nlm.nih.gov/pubmed/27465308 http://dx.doi.org/10.1038/srep30497 |
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author | Dowall, Stuart D. Bosworth, Andrew Rayner, Emma Taylor, Irene Landon, John Cameron, Ian Coxon, Ruth Al Abdulla, Ibrahim Graham, Victoria A. Hall, Graham Kobinger, Gary Hewson, Roger Carroll, Miles W. |
author_facet | Dowall, Stuart D. Bosworth, Andrew Rayner, Emma Taylor, Irene Landon, John Cameron, Ian Coxon, Ruth Al Abdulla, Ibrahim Graham, Victoria A. Hall, Graham Kobinger, Gary Hewson, Roger Carroll, Miles W. |
author_sort | Dowall, Stuart D. |
collection | PubMed |
description | Ebola virus (EBOV) is highly pathogenic, with a predisposition to cause outbreaks in human populations accompanied by significant mortality. An ovine polyclonal antibody therapy has been developed against EBOV, named EBOTAb. When tested in the stringent guinea pig model of EBOV disease, EBOTAb has been shown to confer protection at levels of 83.3%, 50% and 33.3% when treatment was first started on days 3, 4 and 5 post-challenge, respectively. These timepoints of when EBOTAb treatment was initiated correspond to when levels of EBOV are detectable in the circulation and thus mimic when treatment would likely be initiated in human infection. The effects of EBOTAb were compared with those of a monoclonal antibody cocktail, ZMapp, when delivered on day 3 post-challenge. Results showed ZMapp to confer complete protection against lethal EBOV challenge in the guinea pig model at this timepoint. The data reported demonstrate that EBOTAb is an effective treatment against EBOV disease, even when delivered late after infection. |
format | Online Article Text |
id | pubmed-4964638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49646382016-08-08 Post-exposure treatment of Ebola virus disease in guinea pigs using EBOTAb, an ovine antibody-based therapeutic Dowall, Stuart D. Bosworth, Andrew Rayner, Emma Taylor, Irene Landon, John Cameron, Ian Coxon, Ruth Al Abdulla, Ibrahim Graham, Victoria A. Hall, Graham Kobinger, Gary Hewson, Roger Carroll, Miles W. Sci Rep Article Ebola virus (EBOV) is highly pathogenic, with a predisposition to cause outbreaks in human populations accompanied by significant mortality. An ovine polyclonal antibody therapy has been developed against EBOV, named EBOTAb. When tested in the stringent guinea pig model of EBOV disease, EBOTAb has been shown to confer protection at levels of 83.3%, 50% and 33.3% when treatment was first started on days 3, 4 and 5 post-challenge, respectively. These timepoints of when EBOTAb treatment was initiated correspond to when levels of EBOV are detectable in the circulation and thus mimic when treatment would likely be initiated in human infection. The effects of EBOTAb were compared with those of a monoclonal antibody cocktail, ZMapp, when delivered on day 3 post-challenge. Results showed ZMapp to confer complete protection against lethal EBOV challenge in the guinea pig model at this timepoint. The data reported demonstrate that EBOTAb is an effective treatment against EBOV disease, even when delivered late after infection. Nature Publishing Group 2016-07-28 /pmc/articles/PMC4964638/ /pubmed/27465308 http://dx.doi.org/10.1038/srep30497 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Dowall, Stuart D. Bosworth, Andrew Rayner, Emma Taylor, Irene Landon, John Cameron, Ian Coxon, Ruth Al Abdulla, Ibrahim Graham, Victoria A. Hall, Graham Kobinger, Gary Hewson, Roger Carroll, Miles W. Post-exposure treatment of Ebola virus disease in guinea pigs using EBOTAb, an ovine antibody-based therapeutic |
title | Post-exposure treatment of Ebola virus disease in guinea pigs using EBOTAb, an ovine antibody-based therapeutic |
title_full | Post-exposure treatment of Ebola virus disease in guinea pigs using EBOTAb, an ovine antibody-based therapeutic |
title_fullStr | Post-exposure treatment of Ebola virus disease in guinea pigs using EBOTAb, an ovine antibody-based therapeutic |
title_full_unstemmed | Post-exposure treatment of Ebola virus disease in guinea pigs using EBOTAb, an ovine antibody-based therapeutic |
title_short | Post-exposure treatment of Ebola virus disease in guinea pigs using EBOTAb, an ovine antibody-based therapeutic |
title_sort | post-exposure treatment of ebola virus disease in guinea pigs using ebotab, an ovine antibody-based therapeutic |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4964638/ https://www.ncbi.nlm.nih.gov/pubmed/27465308 http://dx.doi.org/10.1038/srep30497 |
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