An inactivated multivalent influenza A virus vaccine is broadly protective in mice and ferrets

Author:

Park Jaekeun1ORCID,Fong Legaspi Sharon L.1ORCID,Schwartzman Louis M.1,Gygli Sebastian M.1,Sheng Zhong-Mei1ORCID,Freeman Ashley D.1ORCID,Matthews Lex M.1ORCID,Xiao Yongli1,Ramuta Mitchell D.1ORCID,Batchenkova Natalia A.1,Qi Li1ORCID,Rosas Luz Angela1ORCID,Williams Stephanie L.1ORCID,Scherler Kelsey2ORCID,Gouzoulis Monica3,Bellayr Ian4,Morens David M.5ORCID,Walters Kathie-Anne2ORCID,Memoli Matthew J.3ORCID,Kash John C.1ORCID,Taubenberger Jeffery K.1ORCID

Affiliation:

1. Viral Pathogenesis and Evolution Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

2. Institute for Systems Biology, Seattle, WA 98109, USA.

3. Clinical Studies Unit, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

4. Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892 USA.

5. Office of the Director, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

Abstract

Influenza A viruses (IAVs) present major public health threats from annual seasonal epidemics and pandemics and from viruses adapted to a variety of animals including poultry, pigs, and horses. Vaccines that broadly protect against all such IAVs, so-called “universal” influenza vaccines, do not currently exist but are urgently needed. Here, we demonstrated that an inactivated, multivalent whole-virus vaccine, delivered intramuscularly or intranasally, was broadly protective against challenges with multiple IAV hemagglutinin and neuraminidase subtypes in both mice and ferrets. The vaccine is composed of four β-propiolactone–inactivated low-pathogenicity avian IAV subtypes of H1N9, H3N8, H5N1, and H7N3. Vaccinated mice and ferrets demonstrated substantial protection against a variety of IAVs, including the 1918 H1N1 strain, the highly pathogenic avian H5N8 strain, and H7N9. We also observed protection against challenge with antigenically variable and heterosubtypic avian, swine, and human viruses. Compared to control animals, vaccinated mice and ferrets demonstrated marked reductions in viral titers, lung pathology, and host inflammatory responses. This vaccine approach indicates the feasibility of eliciting broad, heterosubtypic IAV protection and identifies a promising candidate for influenza vaccine clinical development.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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