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A Single Dose of NILV-Based Vaccine Provides Rapid and Durable Protection against Zika Virus
Zika virus, a member of the Flaviviridae family, is primarily transmitted by infected Aedes species mosquitoes. In 2016, Zika infection emerged as a global health emergency for its explosive spread and the remarkable neurological defects in the developing fetus. Development of a safe and effective Z...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Society of Gene & Cell Therapy
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403329/ https://www.ncbi.nlm.nih.gov/pubmed/32485138 http://dx.doi.org/10.1016/j.ymthe.2020.05.016 |
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author | Ku, Min Wen Anna, François Souque, Philippe Petres, Stéphane Prot, Matthieu Simon-Loriere, Etienne Charneau, Pierre Bourgine, Maryline |
author_facet | Ku, Min Wen Anna, François Souque, Philippe Petres, Stéphane Prot, Matthieu Simon-Loriere, Etienne Charneau, Pierre Bourgine, Maryline |
author_sort | Ku, Min Wen |
collection | PubMed |
description | Zika virus, a member of the Flaviviridae family, is primarily transmitted by infected Aedes species mosquitoes. In 2016, Zika infection emerged as a global health emergency for its explosive spread and the remarkable neurological defects in the developing fetus. Development of a safe and effective Zika vaccine remains a high priority owing to the risk of re-emergence and limited understanding of Zika virus epidemiology. We engineered a non-integrating lentiviralvector(NILV)-based Zika vaccine encoding the consensus pre-membrane and envelope glycoprotein of circulating Zika virus strains. We further evaluated the immunogenicity and protective efficacy of this vaccine in both immunocompromised and immunocompetent mouse models. A single immunization in both mouse models elicited a robust neutralizing antibody titer and afforded full protection against Zika challenge as early as 7 days post-immunization. This NILV-based vaccine also induced a long-lasting immunity when immunized mice were challenged 6 months after immunization. Altogether, our NILV Zika vaccine provides a rapid yet durable protection through a single dose of immunization without extra adjuvant formulation. Our data suggest a promising Zika vaccine candidate for an emergency situation, and demonstrate the capacity of lentiviral vector as an efficient vaccine delivery platform. |
format | Online Article Text |
id | pubmed-7403329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-74033292021-08-05 A Single Dose of NILV-Based Vaccine Provides Rapid and Durable Protection against Zika Virus Ku, Min Wen Anna, François Souque, Philippe Petres, Stéphane Prot, Matthieu Simon-Loriere, Etienne Charneau, Pierre Bourgine, Maryline Mol Ther Original Article Zika virus, a member of the Flaviviridae family, is primarily transmitted by infected Aedes species mosquitoes. In 2016, Zika infection emerged as a global health emergency for its explosive spread and the remarkable neurological defects in the developing fetus. Development of a safe and effective Zika vaccine remains a high priority owing to the risk of re-emergence and limited understanding of Zika virus epidemiology. We engineered a non-integrating lentiviralvector(NILV)-based Zika vaccine encoding the consensus pre-membrane and envelope glycoprotein of circulating Zika virus strains. We further evaluated the immunogenicity and protective efficacy of this vaccine in both immunocompromised and immunocompetent mouse models. A single immunization in both mouse models elicited a robust neutralizing antibody titer and afforded full protection against Zika challenge as early as 7 days post-immunization. This NILV-based vaccine also induced a long-lasting immunity when immunized mice were challenged 6 months after immunization. Altogether, our NILV Zika vaccine provides a rapid yet durable protection through a single dose of immunization without extra adjuvant formulation. Our data suggest a promising Zika vaccine candidate for an emergency situation, and demonstrate the capacity of lentiviral vector as an efficient vaccine delivery platform. American Society of Gene & Cell Therapy 2020-08-05 2020-05-20 /pmc/articles/PMC7403329/ /pubmed/32485138 http://dx.doi.org/10.1016/j.ymthe.2020.05.016 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Ku, Min Wen Anna, François Souque, Philippe Petres, Stéphane Prot, Matthieu Simon-Loriere, Etienne Charneau, Pierre Bourgine, Maryline A Single Dose of NILV-Based Vaccine Provides Rapid and Durable Protection against Zika Virus |
title | A Single Dose of NILV-Based Vaccine Provides Rapid and Durable Protection against Zika Virus |
title_full | A Single Dose of NILV-Based Vaccine Provides Rapid and Durable Protection against Zika Virus |
title_fullStr | A Single Dose of NILV-Based Vaccine Provides Rapid and Durable Protection against Zika Virus |
title_full_unstemmed | A Single Dose of NILV-Based Vaccine Provides Rapid and Durable Protection against Zika Virus |
title_short | A Single Dose of NILV-Based Vaccine Provides Rapid and Durable Protection against Zika Virus |
title_sort | single dose of nilv-based vaccine provides rapid and durable protection against zika virus |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403329/ https://www.ncbi.nlm.nih.gov/pubmed/32485138 http://dx.doi.org/10.1016/j.ymthe.2020.05.016 |
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