Respiratory Vaccination with Hemagglutinin Nanoliposomes Protects Mice from Homologous and Heterologous Strains of Influenza Virus

Author:

Sia Zachary R.1,Chiem Kevin23,Huang Wei-Chiao1,Seffouh Amal4,Teimouri Dereshgi Amir56,Hogan Tara56,Ortega Joaquin4,Davidson Bruce A.56ORCID,Martinez-Sobrido Luis23ORCID,Lovell Jonathan F.1ORCID

Affiliation:

1. Department of Biomedical Engineering, University at Buffalo, State University of New York, Buffalo, New York, USA

2. Texas Biomedical Research Institute, San Antonio, Texas, USA

3. Department of Microbiology and Immunology, University of Rochester, Rochester, New York, USA

4. Department of Anatomy and Cell Biology, McGill University, Montreal, Quebec, Canada

5. Veterans Administration Western New York Healthcare System, Buffalo, New York, USA

6. Department of Anesthesiology, University at Buffalo, State University of New York, Buffalo, New York, USA

Abstract

A self-assembling influenza virus vaccine platform that seamlessly converts soluble antigens into nanoparticles is demonstrated with various H1N1 and H3N2 influenza antigens to protect mice against influenza virus challenge following intranasal vaccination. Mucosal immune responses following liposome delivery to lung antigen-presenting cells are demonstrated.

Funder

HHS | National Institutes of Health

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

Reference37 articles.

1. Centers for Disease Control and Prevention. 2022. CDC seasonal flu vaccine effectiveness studies. https://www.cdc.gov/flu/vaccines-work/effectiveness-studies.htm. Accessed 3 August 2022.

2. Centers for Disease Control and Prevention. 2021. Flu vaccination coverage United States 2020–2021 influenza season. https://www.cdc.gov/flu/fluvaxview/coverage-2021estimates.htm. Accessed 7 October 2021.

3. Mucosal Delivery of Inactivated Influenza Vaccine Induces B-Cell-Dependent Heterosubtypic Cross-Protection against Lethal Influenza A H5N1 Virus Infection

4. Intranasal Influenza Vaccine in a Working Population

5. A double-blind trial of a new inactivated, trivalent, intra-nasal anti-influenza vaccine in general practice: relationship between immunogenicity and respiratory morbidity over the winter of 1997–98

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