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Development of a Cost-effective Ovine Polyclonal Antibody-Based Product, EBOTAb, to Treat Ebola Virus Infection
The highly glycosylated glycoprotein spike of Ebola virus (EBOV-GP(1,2)) is the primary target of the humoral host response. Recombinant EBOV-GP ectodomain (EBOV-GP(1,2ecto)) expressed in mammalian cells was used to immunize sheep and elicited a robust immune response and produced high titers of hig...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779302/ https://www.ncbi.nlm.nih.gov/pubmed/26715676 http://dx.doi.org/10.1093/infdis/jiv565 |
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author | Dowall, Stuart David Callan, Jo Zeltina, Antra Al-Abdulla, Ibrahim Strecker, Thomas Fehling, Sarah K. Krähling, Verena Bosworth, Andrew Rayner, Emma Taylor, Irene Charlton, Sue Landon, John Cameron, Ian Hewson, Roger Nasidi, Abdulsalami Bowden, Thomas A. Carroll, Miles W. |
author_facet | Dowall, Stuart David Callan, Jo Zeltina, Antra Al-Abdulla, Ibrahim Strecker, Thomas Fehling, Sarah K. Krähling, Verena Bosworth, Andrew Rayner, Emma Taylor, Irene Charlton, Sue Landon, John Cameron, Ian Hewson, Roger Nasidi, Abdulsalami Bowden, Thomas A. Carroll, Miles W. |
author_sort | Dowall, Stuart David |
collection | PubMed |
description | The highly glycosylated glycoprotein spike of Ebola virus (EBOV-GP(1,2)) is the primary target of the humoral host response. Recombinant EBOV-GP ectodomain (EBOV-GP(1,2ecto)) expressed in mammalian cells was used to immunize sheep and elicited a robust immune response and produced high titers of high avidity polyclonal antibodies. Investigation of the neutralizing activity of the ovine antisera in vitro revealed that it neutralized EBOV. A pool of intact ovine immunoglobulin G, herein termed EBOTAb, was prepared from the antisera and used for an in vivo guinea pig study. When EBOTAb was delivered 6 hours after challenge, all animals survived without experiencing fever or other clinical manifestations. In a second series of guinea pig studies, the administration of EBOTAb dosing was delayed for 48 or 72 hours after challenge, resulting in 100% and 75% survival, respectively. These studies illustrate the usefulness of EBOTAb in protecting against EBOV-induced disease. |
format | Online Article Text |
id | pubmed-4779302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47793022016-03-07 Development of a Cost-effective Ovine Polyclonal Antibody-Based Product, EBOTAb, to Treat Ebola Virus Infection Dowall, Stuart David Callan, Jo Zeltina, Antra Al-Abdulla, Ibrahim Strecker, Thomas Fehling, Sarah K. Krähling, Verena Bosworth, Andrew Rayner, Emma Taylor, Irene Charlton, Sue Landon, John Cameron, Ian Hewson, Roger Nasidi, Abdulsalami Bowden, Thomas A. Carroll, Miles W. J Infect Dis Major Articles and Brief Reports The highly glycosylated glycoprotein spike of Ebola virus (EBOV-GP(1,2)) is the primary target of the humoral host response. Recombinant EBOV-GP ectodomain (EBOV-GP(1,2ecto)) expressed in mammalian cells was used to immunize sheep and elicited a robust immune response and produced high titers of high avidity polyclonal antibodies. Investigation of the neutralizing activity of the ovine antisera in vitro revealed that it neutralized EBOV. A pool of intact ovine immunoglobulin G, herein termed EBOTAb, was prepared from the antisera and used for an in vivo guinea pig study. When EBOTAb was delivered 6 hours after challenge, all animals survived without experiencing fever or other clinical manifestations. In a second series of guinea pig studies, the administration of EBOTAb dosing was delayed for 48 or 72 hours after challenge, resulting in 100% and 75% survival, respectively. These studies illustrate the usefulness of EBOTAb in protecting against EBOV-induced disease. Oxford University Press 2016-04-01 2015-12-28 /pmc/articles/PMC4779302/ /pubmed/26715676 http://dx.doi.org/10.1093/infdis/jiv565 Text en © The Author 2015. Published by Oxford University Press for the Infectious Diseases Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Major Articles and Brief Reports Dowall, Stuart David Callan, Jo Zeltina, Antra Al-Abdulla, Ibrahim Strecker, Thomas Fehling, Sarah K. Krähling, Verena Bosworth, Andrew Rayner, Emma Taylor, Irene Charlton, Sue Landon, John Cameron, Ian Hewson, Roger Nasidi, Abdulsalami Bowden, Thomas A. Carroll, Miles W. Development of a Cost-effective Ovine Polyclonal Antibody-Based Product, EBOTAb, to Treat Ebola Virus Infection |
title | Development of a Cost-effective Ovine Polyclonal Antibody-Based Product, EBOTAb, to Treat Ebola Virus Infection |
title_full | Development of a Cost-effective Ovine Polyclonal Antibody-Based Product, EBOTAb, to Treat Ebola Virus Infection |
title_fullStr | Development of a Cost-effective Ovine Polyclonal Antibody-Based Product, EBOTAb, to Treat Ebola Virus Infection |
title_full_unstemmed | Development of a Cost-effective Ovine Polyclonal Antibody-Based Product, EBOTAb, to Treat Ebola Virus Infection |
title_short | Development of a Cost-effective Ovine Polyclonal Antibody-Based Product, EBOTAb, to Treat Ebola Virus Infection |
title_sort | development of a cost-effective ovine polyclonal antibody-based product, ebotab, to treat ebola virus infection |
topic | Major Articles and Brief Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779302/ https://www.ncbi.nlm.nih.gov/pubmed/26715676 http://dx.doi.org/10.1093/infdis/jiv565 |
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