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Production of Potent Fully Human Polyclonal Antibodies against Ebola Zaire Virus in Transchromosomal Cattle

Polyclonal antibodies, derived from humans or hyperimmunized animals, have been used prophylactically or therapeutically as countermeasures for a variety of infectious diseases. SAB Biotherapeutics has successfully developed a transchromosomic (Tc) bovine platform technology that can produce fully h...

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Autores principales: Dye, John M., Wu, Hua, Hooper, Jay W., Khurana, Surender, Kuehne, Ana I., Coyle, Elizabeth M., Ortiz, Ramon A., Fuentes, Sandra, Herbert, Andrew S., Golding, Hana, Bakken, Russell A., Brannan, Jennifer M., Kwilas, Steve A., Sullivan, Eddie J., Luke, Thomas C., Smith, Gale, Glenn, Gregory, Li, Wenfang, Ye, Ling, Yang, Chinglai, Compans, Richard W., Tripp, Ralph A., Jiao, Jin-an
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4842964/
https://www.ncbi.nlm.nih.gov/pubmed/27109916
http://dx.doi.org/10.1038/srep24897
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author Dye, John M.
Wu, Hua
Hooper, Jay W.
Khurana, Surender
Kuehne, Ana I.
Coyle, Elizabeth M.
Ortiz, Ramon A.
Fuentes, Sandra
Herbert, Andrew S.
Golding, Hana
Bakken, Russell A.
Brannan, Jennifer M.
Kwilas, Steve A.
Sullivan, Eddie J.
Luke, Thomas C.
Smith, Gale
Glenn, Gregory
Li, Wenfang
Ye, Ling
Yang, Chinglai
Compans, Richard W.
Tripp, Ralph A.
Jiao, Jin-an
author_facet Dye, John M.
Wu, Hua
Hooper, Jay W.
Khurana, Surender
Kuehne, Ana I.
Coyle, Elizabeth M.
Ortiz, Ramon A.
Fuentes, Sandra
Herbert, Andrew S.
Golding, Hana
Bakken, Russell A.
Brannan, Jennifer M.
Kwilas, Steve A.
Sullivan, Eddie J.
Luke, Thomas C.
Smith, Gale
Glenn, Gregory
Li, Wenfang
Ye, Ling
Yang, Chinglai
Compans, Richard W.
Tripp, Ralph A.
Jiao, Jin-an
author_sort Dye, John M.
collection PubMed
description Polyclonal antibodies, derived from humans or hyperimmunized animals, have been used prophylactically or therapeutically as countermeasures for a variety of infectious diseases. SAB Biotherapeutics has successfully developed a transchromosomic (Tc) bovine platform technology that can produce fully human immunoglobulins rapidly, and in substantial quantities, against a variety of disease targets. In this study, two Tc bovines expressing high levels of fully human IgG were hyperimmunized with a recombinant glycoprotein (GP) vaccine consisting of the 2014 Ebola virus (EBOV) Makona isolate. Serum collected from these hyperimmunized Tc bovines contained high titers of human IgG against EBOV GP as determined by GP specific ELISA, surface plasmon resonance (SPR), and virus neutralization assays. Fully human polyclonal antibodies against EBOV were purified and evaluated in a mouse challenge model using mouse adapted Ebola virus (maEBOV). Intraperitoneal administration of the purified anti-EBOV IgG (100 mg/kg) to BALB/c mice one day after lethal challenge with maEBOV resulted in 90% protection; whereas 100% of the control animals succumbed. The results show that hyperimmunization of Tc bovines with EBOV GP can elicit protective and potent neutralizing fully human IgG antibodies rapidly and in commercially viable quantities.
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spelling pubmed-48429642016-04-29 Production of Potent Fully Human Polyclonal Antibodies against Ebola Zaire Virus in Transchromosomal Cattle Dye, John M. Wu, Hua Hooper, Jay W. Khurana, Surender Kuehne, Ana I. Coyle, Elizabeth M. Ortiz, Ramon A. Fuentes, Sandra Herbert, Andrew S. Golding, Hana Bakken, Russell A. Brannan, Jennifer M. Kwilas, Steve A. Sullivan, Eddie J. Luke, Thomas C. Smith, Gale Glenn, Gregory Li, Wenfang Ye, Ling Yang, Chinglai Compans, Richard W. Tripp, Ralph A. Jiao, Jin-an Sci Rep Article Polyclonal antibodies, derived from humans or hyperimmunized animals, have been used prophylactically or therapeutically as countermeasures for a variety of infectious diseases. SAB Biotherapeutics has successfully developed a transchromosomic (Tc) bovine platform technology that can produce fully human immunoglobulins rapidly, and in substantial quantities, against a variety of disease targets. In this study, two Tc bovines expressing high levels of fully human IgG were hyperimmunized with a recombinant glycoprotein (GP) vaccine consisting of the 2014 Ebola virus (EBOV) Makona isolate. Serum collected from these hyperimmunized Tc bovines contained high titers of human IgG against EBOV GP as determined by GP specific ELISA, surface plasmon resonance (SPR), and virus neutralization assays. Fully human polyclonal antibodies against EBOV were purified and evaluated in a mouse challenge model using mouse adapted Ebola virus (maEBOV). Intraperitoneal administration of the purified anti-EBOV IgG (100 mg/kg) to BALB/c mice one day after lethal challenge with maEBOV resulted in 90% protection; whereas 100% of the control animals succumbed. The results show that hyperimmunization of Tc bovines with EBOV GP can elicit protective and potent neutralizing fully human IgG antibodies rapidly and in commercially viable quantities. Nature Publishing Group 2016-04-25 /pmc/articles/PMC4842964/ /pubmed/27109916 http://dx.doi.org/10.1038/srep24897 Text en Copyright © 2016, Macmillan Publishers Limited 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
Dye, John M.
Wu, Hua
Hooper, Jay W.
Khurana, Surender
Kuehne, Ana I.
Coyle, Elizabeth M.
Ortiz, Ramon A.
Fuentes, Sandra
Herbert, Andrew S.
Golding, Hana
Bakken, Russell A.
Brannan, Jennifer M.
Kwilas, Steve A.
Sullivan, Eddie J.
Luke, Thomas C.
Smith, Gale
Glenn, Gregory
Li, Wenfang
Ye, Ling
Yang, Chinglai
Compans, Richard W.
Tripp, Ralph A.
Jiao, Jin-an
Production of Potent Fully Human Polyclonal Antibodies against Ebola Zaire Virus in Transchromosomal Cattle
title Production of Potent Fully Human Polyclonal Antibodies against Ebola Zaire Virus in Transchromosomal Cattle
title_full Production of Potent Fully Human Polyclonal Antibodies against Ebola Zaire Virus in Transchromosomal Cattle
title_fullStr Production of Potent Fully Human Polyclonal Antibodies against Ebola Zaire Virus in Transchromosomal Cattle
title_full_unstemmed Production of Potent Fully Human Polyclonal Antibodies against Ebola Zaire Virus in Transchromosomal Cattle
title_short Production of Potent Fully Human Polyclonal Antibodies against Ebola Zaire Virus in Transchromosomal Cattle
title_sort production of potent fully human polyclonal antibodies against ebola zaire virus in transchromosomal cattle
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4842964/
https://www.ncbi.nlm.nih.gov/pubmed/27109916
http://dx.doi.org/10.1038/srep24897
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