| Literature DB >> 34108251 |
Mathieu Mateo1,2, Stéphanie Reynard1,2, Alexandra Journeaux1,2, Clara Germain1,2, Jimmy Hortion1,2, Xavier Carnec1,2, Caroline Picard1,2, Nicolas Baillet1,2, Virginie Borges-Cardoso1,2, Othmann Merabet1,2, Audrey Vallve3, Stéphane Barron3, Ophélie Jourjon3, Orianne Lacroix3, Aurélie Duthey3, Manon Dirheimer4, Gregory Jouvion5,6, Pierre-Henri Moreau7, Lyne Fellmann7, Caroline Carbonnelle3, Hervé Raoul3, Frédéric Tangy8, Sylvain Baize9,2.
Abstract
A safe and protective Lassa virus vaccine is crucially needed in Western Africa to stem the recurrent outbreaks of Lassa virus infections in Nigeria and the emergence of Lassa virus in previously unaffected countries, such as Benin and Togo. Major challenges in developing a Lassa virus vaccine include the high diversity of circulating strains and their reemergence from 1 year to another. To address each of these challenges, we immunized cynomolgus monkeys with a measles virus vector expressing the Lassa virus glycoprotein and nucleoprotein of the prototypic Lassa virus strain Josiah (MeV-NP). To evaluate vaccine efficacy against heterologous strains of Lassa virus, we challenged the monkeys a month later with heterologous strains from lineage II or lineage VII, finding that the vaccine was protective against these strains. A second cohort of monkeys was challenged 1 year later with the homologous Josiah strain, finding that a single dose of MeV-NP was sufficient to protect all vaccinated monkeys. These studies demonstrate that MeV-NP can generate both long-lasting immune responses and responses that are able to protect against diverse strains of Lassa virus.Entities:
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Year: 2021 PMID: 34108251 DOI: 10.1126/scitranslmed.abf6348
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956