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Purified Inactivated Zika Vaccine Candidates Afford Protection against Lethal Challenge in Mice

In response to the 2016 global public health emergency of international concern announced by the World Health Organization surrounding Zika virus (ZIKV) outbreaks, we developed a purified inactivated Zika virus vaccine (PIZV) candidate from ZIKV strain PRVABC59, isolated during the outbreak in 2015....

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Autores principales: Baldwin, Whitney R., Livengood, Jill A., Giebler, Holli A., Stovall, Janae L., Boroughs, Karen L., Sonnberg, Stephanie, Bohning, Kelly J., Dietrich, Elizabeth A., Ong, Yee Tsuey, Danh, Hoang K., Patel, Hetal K., Huang, Claire Y.-H., Dean, Hansi J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220238/
https://www.ncbi.nlm.nih.gov/pubmed/30405178
http://dx.doi.org/10.1038/s41598-018-34735-7
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author Baldwin, Whitney R.
Livengood, Jill A.
Giebler, Holli A.
Stovall, Janae L.
Boroughs, Karen L.
Sonnberg, Stephanie
Bohning, Kelly J.
Dietrich, Elizabeth A.
Ong, Yee Tsuey
Danh, Hoang K.
Patel, Hetal K.
Huang, Claire Y.-H.
Dean, Hansi J.
author_facet Baldwin, Whitney R.
Livengood, Jill A.
Giebler, Holli A.
Stovall, Janae L.
Boroughs, Karen L.
Sonnberg, Stephanie
Bohning, Kelly J.
Dietrich, Elizabeth A.
Ong, Yee Tsuey
Danh, Hoang K.
Patel, Hetal K.
Huang, Claire Y.-H.
Dean, Hansi J.
author_sort Baldwin, Whitney R.
collection PubMed
description In response to the 2016 global public health emergency of international concern announced by the World Health Organization surrounding Zika virus (ZIKV) outbreaks, we developed a purified inactivated Zika virus vaccine (PIZV) candidate from ZIKV strain PRVABC59, isolated during the outbreak in 2015. The virus isolate was plaque purified, creating six sub-isolated virus stocks, two of which were selected to generate PIZV candidates for preclinical immunogenicity and efficacy evaluation in mice. The alum-adjuvanted PIZV candidates were highly immunogenic in both CD-1 and AG129 mice after a 2-dose immunization. Further, AG129 mice receiving 2 doses of PIZV formulated with alum were fully protected against lethal ZIKV challenge and mouse immune sera elicited by the PIZV candidates were capable of neutralizing ZIKVs of both African and Asian genetic lineages in vitro. Additionally, passive immunization of naïve mice with ZIKV-immune serum showed strong positive correlation between neutralizing ZIKV antibody (NAb) titers and protection against lethal challenge. This study supported advancement of the PIZV candidate toward clinical development.
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spelling pubmed-62202382018-11-08 Purified Inactivated Zika Vaccine Candidates Afford Protection against Lethal Challenge in Mice Baldwin, Whitney R. Livengood, Jill A. Giebler, Holli A. Stovall, Janae L. Boroughs, Karen L. Sonnberg, Stephanie Bohning, Kelly J. Dietrich, Elizabeth A. Ong, Yee Tsuey Danh, Hoang K. Patel, Hetal K. Huang, Claire Y.-H. Dean, Hansi J. Sci Rep Article In response to the 2016 global public health emergency of international concern announced by the World Health Organization surrounding Zika virus (ZIKV) outbreaks, we developed a purified inactivated Zika virus vaccine (PIZV) candidate from ZIKV strain PRVABC59, isolated during the outbreak in 2015. The virus isolate was plaque purified, creating six sub-isolated virus stocks, two of which were selected to generate PIZV candidates for preclinical immunogenicity and efficacy evaluation in mice. The alum-adjuvanted PIZV candidates were highly immunogenic in both CD-1 and AG129 mice after a 2-dose immunization. Further, AG129 mice receiving 2 doses of PIZV formulated with alum were fully protected against lethal ZIKV challenge and mouse immune sera elicited by the PIZV candidates were capable of neutralizing ZIKVs of both African and Asian genetic lineages in vitro. Additionally, passive immunization of naïve mice with ZIKV-immune serum showed strong positive correlation between neutralizing ZIKV antibody (NAb) titers and protection against lethal challenge. This study supported advancement of the PIZV candidate toward clinical development. Nature Publishing Group UK 2018-11-07 /pmc/articles/PMC6220238/ /pubmed/30405178 http://dx.doi.org/10.1038/s41598-018-34735-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Baldwin, Whitney R.
Livengood, Jill A.
Giebler, Holli A.
Stovall, Janae L.
Boroughs, Karen L.
Sonnberg, Stephanie
Bohning, Kelly J.
Dietrich, Elizabeth A.
Ong, Yee Tsuey
Danh, Hoang K.
Patel, Hetal K.
Huang, Claire Y.-H.
Dean, Hansi J.
Purified Inactivated Zika Vaccine Candidates Afford Protection against Lethal Challenge in Mice
title Purified Inactivated Zika Vaccine Candidates Afford Protection against Lethal Challenge in Mice
title_full Purified Inactivated Zika Vaccine Candidates Afford Protection against Lethal Challenge in Mice
title_fullStr Purified Inactivated Zika Vaccine Candidates Afford Protection against Lethal Challenge in Mice
title_full_unstemmed Purified Inactivated Zika Vaccine Candidates Afford Protection against Lethal Challenge in Mice
title_short Purified Inactivated Zika Vaccine Candidates Afford Protection against Lethal Challenge in Mice
title_sort purified inactivated zika vaccine candidates afford protection against lethal challenge in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220238/
https://www.ncbi.nlm.nih.gov/pubmed/30405178
http://dx.doi.org/10.1038/s41598-018-34735-7
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