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Post-Exposure Protection in Mice against Sudan Virus by a Two Antibody Cocktail

Sudan virus (SUDV) and Ebola viruses (EBOV) are both members of the Ebolavirus genus and have been sources of epidemics and outbreaks for several decades. We present here the generation and characterization of cross-reactive antibodies to both SUDV and EBOV, which were produced in a cell-free system...

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Autores principales: Froude, Jeffrey W., Herbert, Andrew S., Pelat, Thibaut, Miethe, Sebastian, Zak, Samantha E., Brannan, Jennifer M., Bakken, Russell R., Steiner, Alexander R., Yin, Gang, Hallam, Trevor J., Sato, Aaron K., Hust, Michael, Thullier, Philippe, Dye, John M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6024315/
https://www.ncbi.nlm.nih.gov/pubmed/29861435
http://dx.doi.org/10.3390/v10060286
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author Froude, Jeffrey W.
Herbert, Andrew S.
Pelat, Thibaut
Miethe, Sebastian
Zak, Samantha E.
Brannan, Jennifer M.
Bakken, Russell R.
Steiner, Alexander R.
Yin, Gang
Hallam, Trevor J.
Sato, Aaron K.
Hust, Michael
Thullier, Philippe
Dye, John M.
author_facet Froude, Jeffrey W.
Herbert, Andrew S.
Pelat, Thibaut
Miethe, Sebastian
Zak, Samantha E.
Brannan, Jennifer M.
Bakken, Russell R.
Steiner, Alexander R.
Yin, Gang
Hallam, Trevor J.
Sato, Aaron K.
Hust, Michael
Thullier, Philippe
Dye, John M.
author_sort Froude, Jeffrey W.
collection PubMed
description Sudan virus (SUDV) and Ebola viruses (EBOV) are both members of the Ebolavirus genus and have been sources of epidemics and outbreaks for several decades. We present here the generation and characterization of cross-reactive antibodies to both SUDV and EBOV, which were produced in a cell-free system and protective against SUDV in mice. A non-human primate, cynomolgus macaque, was immunized with viral-replicon particles expressing the glycoprotein of SUDV-Boniface (8A). Two separate antibody fragment phage display libraries were constructed after four immunogen injections. Both libraries were screened first against the SUDV and a second library was cross-selected against EBOV-Kikwit. Sequencing of 288 selected clones from the two distinct libraries identified 58 clones with distinct V(H) and V(L) sequences. Many of these clones were cross-reactive to EBOV and SUDV and able to neutralize SUDV. Three of these recombinant antibodies (X10B1, X10F3, and X10H2) were produced in the scFv-Fc format utilizing a cell-free production system. Mice that were challenged with SUDV-Boniface receiving 100µg of the X10B1/X10H2 scFv-Fc combination 6 and 48-h post-exposure demonstrated partial protection individually and complete protection as a combination. The data herein suggests these antibodies may be promising candidates for further therapeutic development.
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spelling pubmed-60243152018-07-16 Post-Exposure Protection in Mice against Sudan Virus by a Two Antibody Cocktail Froude, Jeffrey W. Herbert, Andrew S. Pelat, Thibaut Miethe, Sebastian Zak, Samantha E. Brannan, Jennifer M. Bakken, Russell R. Steiner, Alexander R. Yin, Gang Hallam, Trevor J. Sato, Aaron K. Hust, Michael Thullier, Philippe Dye, John M. Viruses Article Sudan virus (SUDV) and Ebola viruses (EBOV) are both members of the Ebolavirus genus and have been sources of epidemics and outbreaks for several decades. We present here the generation and characterization of cross-reactive antibodies to both SUDV and EBOV, which were produced in a cell-free system and protective against SUDV in mice. A non-human primate, cynomolgus macaque, was immunized with viral-replicon particles expressing the glycoprotein of SUDV-Boniface (8A). Two separate antibody fragment phage display libraries were constructed after four immunogen injections. Both libraries were screened first against the SUDV and a second library was cross-selected against EBOV-Kikwit. Sequencing of 288 selected clones from the two distinct libraries identified 58 clones with distinct V(H) and V(L) sequences. Many of these clones were cross-reactive to EBOV and SUDV and able to neutralize SUDV. Three of these recombinant antibodies (X10B1, X10F3, and X10H2) were produced in the scFv-Fc format utilizing a cell-free production system. Mice that were challenged with SUDV-Boniface receiving 100µg of the X10B1/X10H2 scFv-Fc combination 6 and 48-h post-exposure demonstrated partial protection individually and complete protection as a combination. The data herein suggests these antibodies may be promising candidates for further therapeutic development. MDPI 2018-05-26 /pmc/articles/PMC6024315/ /pubmed/29861435 http://dx.doi.org/10.3390/v10060286 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Froude, Jeffrey W.
Herbert, Andrew S.
Pelat, Thibaut
Miethe, Sebastian
Zak, Samantha E.
Brannan, Jennifer M.
Bakken, Russell R.
Steiner, Alexander R.
Yin, Gang
Hallam, Trevor J.
Sato, Aaron K.
Hust, Michael
Thullier, Philippe
Dye, John M.
Post-Exposure Protection in Mice against Sudan Virus by a Two Antibody Cocktail
title Post-Exposure Protection in Mice against Sudan Virus by a Two Antibody Cocktail
title_full Post-Exposure Protection in Mice against Sudan Virus by a Two Antibody Cocktail
title_fullStr Post-Exposure Protection in Mice against Sudan Virus by a Two Antibody Cocktail
title_full_unstemmed Post-Exposure Protection in Mice against Sudan Virus by a Two Antibody Cocktail
title_short Post-Exposure Protection in Mice against Sudan Virus by a Two Antibody Cocktail
title_sort post-exposure protection in mice against sudan virus by a two antibody cocktail
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6024315/
https://www.ncbi.nlm.nih.gov/pubmed/29861435
http://dx.doi.org/10.3390/v10060286
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