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mRNA Vaccine Protects against Zika Virus
Zika virus (ZIKV), a mosquito-borne flavivirus, has recently triggered global concern due to severe health complications. In 2015, a large ZIKV outbreak occurred in the Americas and established a link between ZIKV and microcephaly in newborn babies, spontaneous abortion, persistent viremia, and Guil...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8707647/ https://www.ncbi.nlm.nih.gov/pubmed/34960211 http://dx.doi.org/10.3390/vaccines9121464 |
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author | Medina-Magües, Lex G. Gergen, Janina Jasny, Edith Petsch, Benjamin Lopera-Madrid, Jaime Medina-Magües, Emily S. Salas-Quinchucua, Cristhian Osorio, Jorge E. |
author_facet | Medina-Magües, Lex G. Gergen, Janina Jasny, Edith Petsch, Benjamin Lopera-Madrid, Jaime Medina-Magües, Emily S. Salas-Quinchucua, Cristhian Osorio, Jorge E. |
author_sort | Medina-Magües, Lex G. |
collection | PubMed |
description | Zika virus (ZIKV), a mosquito-borne flavivirus, has recently triggered global concern due to severe health complications. In 2015, a large ZIKV outbreak occurred in the Americas and established a link between ZIKV and microcephaly in newborn babies, spontaneous abortion, persistent viremia, and Guillain–Barré syndrome. While antivirals are being developed and prevention strategies focus on vector control, a safe and effective Zika vaccine remains unavailable. Messenger RNA (mRNA) vaccine technology has arisen as a flexible, simplified, and fast vaccine production platform. Here, we report on an mRNA vaccine candidate that encodes the pre-membrane and envelope (prM–E) glycoproteins of ZIKV strain Brazil SPH2015 and is encapsulated in lipid nanoparticles (LNPs). Our ZIKV prM–E mRNA-LNP vaccine candidate induced antibody responses that protected in AG129 mice deficient in interferon (IFN) alpha/beta/gamma (IFN-α/β/γ) receptors. Notably, a single administration of ZIKV prM–E mRNA-LNP protected against a lethal dose of ZIKV, while a two-dose strategy induced strong protective immunity. E-specific double-positive IFN-γ and TNF-α T-cells were induced in BALB/c mice after immunizations with a two-dose strategy. With the success of mRNA vaccine technology in facing the coronavirus (COVID-19) pandemic, our data support the development of prM–E RNActive(®) as a promising mRNA vaccine against Zika to counter future epidemics. |
format | Online Article Text |
id | pubmed-8707647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87076472021-12-25 mRNA Vaccine Protects against Zika Virus Medina-Magües, Lex G. Gergen, Janina Jasny, Edith Petsch, Benjamin Lopera-Madrid, Jaime Medina-Magües, Emily S. Salas-Quinchucua, Cristhian Osorio, Jorge E. Vaccines (Basel) Article Zika virus (ZIKV), a mosquito-borne flavivirus, has recently triggered global concern due to severe health complications. In 2015, a large ZIKV outbreak occurred in the Americas and established a link between ZIKV and microcephaly in newborn babies, spontaneous abortion, persistent viremia, and Guillain–Barré syndrome. While antivirals are being developed and prevention strategies focus on vector control, a safe and effective Zika vaccine remains unavailable. Messenger RNA (mRNA) vaccine technology has arisen as a flexible, simplified, and fast vaccine production platform. Here, we report on an mRNA vaccine candidate that encodes the pre-membrane and envelope (prM–E) glycoproteins of ZIKV strain Brazil SPH2015 and is encapsulated in lipid nanoparticles (LNPs). Our ZIKV prM–E mRNA-LNP vaccine candidate induced antibody responses that protected in AG129 mice deficient in interferon (IFN) alpha/beta/gamma (IFN-α/β/γ) receptors. Notably, a single administration of ZIKV prM–E mRNA-LNP protected against a lethal dose of ZIKV, while a two-dose strategy induced strong protective immunity. E-specific double-positive IFN-γ and TNF-α T-cells were induced in BALB/c mice after immunizations with a two-dose strategy. With the success of mRNA vaccine technology in facing the coronavirus (COVID-19) pandemic, our data support the development of prM–E RNActive(®) as a promising mRNA vaccine against Zika to counter future epidemics. MDPI 2021-12-10 /pmc/articles/PMC8707647/ /pubmed/34960211 http://dx.doi.org/10.3390/vaccines9121464 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Medina-Magües, Lex G. Gergen, Janina Jasny, Edith Petsch, Benjamin Lopera-Madrid, Jaime Medina-Magües, Emily S. Salas-Quinchucua, Cristhian Osorio, Jorge E. mRNA Vaccine Protects against Zika Virus |
title | mRNA Vaccine Protects against Zika Virus |
title_full | mRNA Vaccine Protects against Zika Virus |
title_fullStr | mRNA Vaccine Protects against Zika Virus |
title_full_unstemmed | mRNA Vaccine Protects against Zika Virus |
title_short | mRNA Vaccine Protects against Zika Virus |
title_sort | mrna vaccine protects against zika virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8707647/ https://www.ncbi.nlm.nih.gov/pubmed/34960211 http://dx.doi.org/10.3390/vaccines9121464 |
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