A multivalent nucleoside-modified mRNA vaccine against all known influenza virus subtypes

Author:

Arevalo Claudia P.1ORCID,Bolton Marcus J.1ORCID,Le Sage Valerie2ORCID,Ye Naiqing1,Furey Colleen1ORCID,Muramatsu Hiromi1ORCID,Alameh Mohamad-Gabriel3,Pardi Norbert1ORCID,Drapeau Elizabeth M.1ORCID,Parkhouse Kaela1ORCID,Garretson Tyler1,Morris Jeffrey S.4ORCID,Moncla Louise H.5ORCID,Tam Ying K.6ORCID,Fan Steven H. Y.6,Lakdawala Seema S.27ORCID,Weissman Drew3ORCID,Hensley Scott E.1ORCID

Affiliation:

1. Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

2. Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.

3. Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

4. Department of Biostatistics Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

5. Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.

6. Acuitas Therapeutics, Vancouver, BC V6T 1Z3, Canada.

7. Center for Vaccine Research, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.

Abstract

Seasonal influenza vaccines offer little protection against pandemic influenza virus strains. It is difficult to create effective prepandemic vaccines because it is uncertain which influenza virus subtype will cause the next pandemic. In this work, we developed a nucleoside-modified messenger RNA (mRNA)–lipid nanoparticle vaccine encoding hemagglutinin antigens from all 20 known influenza A virus subtypes and influenza B virus lineages. This multivalent vaccine elicited high levels of cross-reactive and subtype-specific antibodies in mice and ferrets that reacted to all 20 encoded antigens. Vaccination protected mice and ferrets challenged with matched and mismatched viral strains, and this protection was at least partially dependent on antibodies. Our studies indicate that mRNA vaccines can provide protection against antigenically variable viruses by simultaneously inducing antibodies against multiple antigens.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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