mRNA Vaccine Protects against Zika Virus.

AG129 RNActive® ZIKV Zika vaccines Zika virus challenge flavivirus lipid nanoparticles mRNA vaccines mice

Journal

Vaccines
ISSN: 2076-393X
Titre abrégé: Vaccines (Basel)
Pays: Switzerland
ID NLM: 101629355

Informations de publication

Date de publication:
10 Dec 2021
Historique:
received: 21 10 2021
revised: 02 12 2021
accepted: 07 12 2021
entrez: 28 12 2021
pubmed: 29 12 2021
medline: 29 12 2021
Statut: epublish

Résumé

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

Identifiants

pubmed: 34960211
pii: vaccines9121464
doi: 10.3390/vaccines9121464
pmc: PMC8707647
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Lex G Medina-Magües (LG)

Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI 53706, USA.

Janina Gergen (J)

CureVac AG, Friedrich-Miescher-Straße 15, 72076 Tübingen, Germany.

Edith Jasny (E)

CureVac AG, Friedrich-Miescher-Straße 15, 72076 Tübingen, Germany.

Benjamin Petsch (B)

CureVac AG, Friedrich-Miescher-Straße 15, 72076 Tübingen, Germany.

Jaime Lopera-Madrid (J)

Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI 53706, USA.

Emily S Medina-Magües (ES)

Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI 53706, USA.

Cristhian Salas-Quinchucua (C)

Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI 53706, USA.

Jorge E Osorio (JE)

Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI 53706, USA.

Classifications MeSH