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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
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.
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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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