More Shots on Goal: Heterologous Influenza Prime-Boost Vaccination Decreases the Likelihood of a Negligible Antibody Response to Current or Historical Variants

Seasonal influenza vaccination only elicits a strong and durable antibody response in a subset of recipients, and prior homologous booster trials have failed to improve on single-dose vaccination. Here, we conducted a phase 4 clinical trial to test if a heterologous prime-boost increases antibody magnitude or breadth as well as reduces the rate of non-responders (ClinicalTrials.gov ID# NCT06567860 ). Participants received a late-season 2023 inactivated influenza vaccine followed by the 2024 booster four months later containing an updated H3N2 strain alongside unchanged H1N1 and B/Victoria strains, allowing within-subject comparison of heterologous and homologous boosting. The booster vaccination halted or reversed antibody titer waning for all vaccine strains, most notably restoring seroprotective and seroconverting titers for B/Victoria at the cohort-level. Critically, the heterologous booster decreased the rate of non-responders (exhibiting HAI≤10 at all time points), with 0% H3N2 non-responders among subjects receiving the prime and boost compared to 29% H1N1 non-responders. A similar pattern held in a larger cohort administering consecutive fall vaccinations, where non-response rate was 20% of H3N2 compared to 37% for H1N1. Across all non-responders that had consistently low titers against the vaccine strains, up to half elicited an antibody response against historical variants, suggesting that immune imprinting partially underlies the non-responder phenotype. Despite differing vaccination timing, late-season priming and standard fall vaccination produced comparable antibody breadth 30 days post-vaccination when cohorts were matched on pre-vaccination titers. These findings suggest that heterologous vaccinations or other multi-strain exposures can reduce the fraction of the population that does not mount an antibody response during an influenza season.

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Publication Details

Journal
medRxiv
Published
2026-10-30
DOI
https://doi.org/10.64898/2026.10.28.26366744
Primary Topic
Influenza Virus Research Studies
Type
preprint

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preprint

More Shots on Goal: Heterologous Influenza Prime-Boost Vaccination Decreases the Likelihood of a Negligible Antibody Response to Current or Historical Variants

Tal Einav, Ted M. Ross, Sierra Orsinelli-Rivers
medRxiv
Influenza Virus Research Studies
preprint

More Shots on Goal: Heterologous Influenza Prime-Boost Vaccination Decreases the Likelihood of a Negligible Antibody Response to Current or Historical Variants

Tal Einav, Ted M. Ross, Sierra Orsinelli-Rivers
preprint en

Abstract

Seasonal influenza vaccination only elicits a strong and durable antibody response in a subset of recipients, and prior homologous booster trials have failed to improve on single-dose vaccination. Here, we conducted a phase 4 clinical trial to test if a heterologous prime-boost increases antibody magnitude or breadth as well as reduces the rate of non-responders (ClinicalTrials.gov ID# NCT06567860 ). Participants received a late-season 2023 inactivated influenza vaccine followed by the 2024 booster four months later containing an updated H3N2 strain alongside unchanged H1N1 and B/Victoria strains, allowing within-subject comparison of heterologous and homologous boosting. The booster vaccination halted or reversed antibody titer waning for all vaccine strains, most notably restoring seroprotective and seroconverting titers for B/Victoria at the cohort-level. Critically, the heterologous booster decreased the rate of non-responders (exhibiting HAI≤10 at all time points), with 0% H3N2 non-responders among subjects receiving the prime and boost compared to 29% H1N1 non-responders. A similar pattern held in a larger cohort administering consecutive fall vaccinations, where non-response rate was 20% of H3N2 compared to 37% for H1N1. Across all non-responders that had consistently low titers against the vaccine strains, up to half elicited an antibody response against historical variants, suggesting that immune imprinting partially underlies the non-responder phenotype. Despite differing vaccination timing, late-season priming and standard fall vaccination produced comparable antibody breadth 30 days post-vaccination when cohorts were matched on pre-vaccination titers. These findings suggest that heterologous vaccinations or other multi-strain exposures can reduce the fraction of the population that does not mount an antibody response during an influenza season.

medRxiv
La Jolla Institute for Immunology (US), Cleveland Clinic (US)
U.S. Department of Health and Human Services, National Institutes of Health, Centers for Disease Control and Prevention, National Institute of Allergy and Infectious Diseases
Good health and well-being
Influenza Virus Research Studies
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