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This entry refers to a specific twice-annual vaccination regimen evaluated by The University of Hong Kong in the RETAIN clinical trial. The strategy involves the administration of inactivated influenza vaccines (IIV) twice a year, utilizing both Northern Hemisphere (NH) and Southern Hemisphere (SH) formulations to provide continuous protection in regions with complex influenza seasonality. The vaccines used in the trial are quadrivalent inactivated influenza vaccines (QIV) manufactured by Sanofi Pasteur, specifically FluQuadri and Vaxigrip. These vaccines contain purified hemagglutinin antigens from four influenza strains (A/H1N1, A/H3N2, and two B lineages). The regimen is designed to address the rapid waning of vaccine-induced immunity in older adults (aged 70-79) by providing a booster effect and updating the strain composition to match circulating viruses in both hemispheres.
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