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Assessment of enhanced influenza vaccination finds that FluAd conveys an advantage in mice and older adults

Authors :
Niloufar Kavian
Asmaa Hachim
Athena PY Li
Carolyn A Cohen
Alex WH Chin
Leo LM Poon
Vicky J Fang
Nancy HL Leung
Benjamin J Cowling
Sophie A Valkenburg
Source :
Clinical & Translational Immunology, Vol 9, Iss 2, Pp n/a-n/a (2020)
Publication Year :
2020
Publisher :
Wiley, 2020.

Abstract

Abstract Objectives Enhanced inactivated influenza vaccines (eIIV) aim to increase immunogenicity and protection compared with the widely used standard IIV (S‐IIV). Methods We tested four vaccines in parallel, FluZone high dose, FluBlok and FluAd versus S‐IIV in a randomised controlled trial of older adults and in a mouse infection model to assess immunogenicity, protection from lethal challenge and mechanisms of action. Results In older adults, FluAd vaccination stimulated a superior antibody profile, including H3‐HA antibodies that were elevated for up to 1 year after vaccination, higher avidity H3HA IgG and larger HA stem IgG responses. In a mouse model, FluAd also elicited an earlier and larger induction of HA stem antibodies with increased germinal centre responses and upregulation and long‐term expression of B‐cell switch transcription factors. Long‐term cross‐reactive memory responses were sustained by FluAd following lethal heterosubtypic influenza challenge, with reduced lung damage and viral loads, coinciding with increased T‐ and B‐cell recall. Advantages were also noted for the high‐dose FluZone vaccine in both humans and mice. Conclusion The early, broadly reactive and long‐lived antibody response of FluAd indicates a potential advantage of this vaccine, particularly in years when there is a mismatch between the vaccine strain and the circulating strain of influenza viruses.

Details

Language :
English
ISSN :
20500068
Volume :
9
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Clinical & Translational Immunology
Publication Type :
Academic Journal
Accession number :
edsdoj.1adf06bc73447db44b2c422cfff16f
Document Type :
article
Full Text :
https://doi.org/10.1002/cti2.1107