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A Single Intramuscular Dose of a Plant-Made Virus-Like Particle Vaccine Elicits a Balanced Humoral and Cellular Response and Protects Young and Aged Mice from Influenza H1N1 Virus Challenge despite a Modest/Absent Humoral Response.

Authors :
Hodgins B
Yam KK
Winter K
Pillet S
Landry N
Ward BJ
Source :
Clinical and vaccine immunology : CVI [Clin Vaccine Immunol] 2017 Dec 05; Vol. 24 (12). Date of Electronic Publication: 2017 Dec 05 (Print Publication: 2017).
Publication Year :
2017

Abstract

Virus-like-particle (VLP) influenza vaccines can be given intramuscularly (i.m.) or intranasally (i.n.) and may have advantages over split-virion formulations in the elderly. We tested a plant-made VLP vaccine candidate bearing the viral hemagglutinin (HA) delivered either i.m. or i.n. in young and aged mice. Young adult (5- to 8-week-old) and aged (16- to 20-month-old) female BALB/c mice received a single 3-μg dose based on the HA (A/California/07/2009 H1N1) content of a plant-made H1-VLP (i.m. or i.n.) split-virion vaccine (i.m.) or were left naive. After vaccination, humoral and splenocyte responses were assessed, and some mice were challenged. Both VLP and split vaccines given i.m. protected 100% of the young animals, but the VLP group lost the least weight and had stronger humoral and cellular responses. Compared to split-vaccine recipients, aged animals vaccinated i.m. with VLP were more likely to survive challenge (80% versus 60%). The lung viral load postchallenge was lowest in the VLP i.m. groups. Mice vaccinated with VLP i.n. had little detectable immune response, but survival was significantly increased. In both age groups, i.m. administration of the H1-VLP vaccine elicited more balanced humoral and cellular responses and provided better protection from homologous challenge than the split-virion vaccine.<br /> (Copyright © 2017 American Society for Microbiology.)

Details

Language :
English
ISSN :
1556-679X
Volume :
24
Issue :
12
Database :
MEDLINE
Journal :
Clinical and vaccine immunology : CVI
Publication Type :
Academic Journal
Accession number :
29021303
Full Text :
https://doi.org/10.1128/CVI.00273-17