Long-term immunogenicity of alternative HPV vaccine schedules and the effect of an additional dose given three to five years post-primary vaccination

We assessed antibody persistence and the impact of an additional dose administered 42-60 months after initial vaccination. Girls initially vaccinated at ages 9-10 with two doses of quadrivalent HPV vaccine participated in two randomized trials: The 0-6-42HPV study which compared a quadrivalent and bivalent additional dose given at 42 months; The 0-6-60ICI-VPH study compared no additional dose to a quadrivalent dose at 60 months. HPV16/18 antibody detection and geometric mean concentrations (GMCs) were assessed (M9ELISA). Overall, 526 girls provided a blood sample. All had detectable HPV16/18 antibodies 10 years post-initial vaccination. An additional dose at 42 versus 60 months led to similar GMCs, both with higher immune responses compared to 2-dose group participants. Compared to the quadrivalent, the bivalent induced significantly higher HPV18 GMCs, which has unknown clinical significance. Two-dose schedule and delayed quadrivalent or bivalent additional doses are highly immunogenic, supporting long-term immunogenicity of alternative and mixed vaccination schedules.

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Publication Details

Journal
Vaccine
Published
2026-02-04
DOI
https://doi.org/10.1016/j.vaccine.2026.128287
Primary Topic
Cervical Cancer and HPV Research
Type
article
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article

Long-term immunogenicity of alternative HPV vaccine schedules and the effect of an additional dose given three to five years post-primary vaccination

Elizabeth R. Unger, Vladimir Gîlca, Gitika Panicker, Iulia Gabriela Ionescu et al.
Vaccine
Cervical Cancer and HPV Research
article

Long-term immunogenicity of alternative HPV vaccine schedules and the effect of an additional dose given three to five years post-primary vaccination

Elizabeth R. Unger, Vladimir Gîlca, Gitika Panicker, Iulia Gabriela Ionescu, Chantal Sauvageau, Marie-Hélène Mayrand, Manale Ouakki
article en

Abstract

We assessed antibody persistence and the impact of an additional dose administered 42-60 months after initial vaccination. Girls initially vaccinated at ages 9-10 with two doses of quadrivalent HPV vaccine participated in two randomized trials: The 0-6-42HPV study which compared a quadrivalent and bivalent additional dose given at 42 months; The 0-6-60ICI-VPH study compared no additional dose to a quadrivalent dose at 60 months. HPV16/18 antibody detection and geometric mean concentrations (GMCs) were assessed (M9ELISA). Overall, 526 girls provided a blood sample. All had detectable HPV16/18 antibodies 10 years post-initial vaccination. An additional dose at 42 versus 60 months led to similar GMCs, both with higher immune responses compared to 2-dose group participants. Compared to the quadrivalent, the bivalent induced significantly higher HPV18 GMCs, which has unknown clinical significance. Two-dose schedule and delayed quadrivalent or bivalent additional doses are highly immunogenic, supporting long-term immunogenicity of alternative and mixed vaccination schedules.

VaccineVol. 75
Centers for Disease Control and Prevention (US), Centre hospitalier universitaire de Québec (CA), Institut National de Santé Publique du Québec (CA), National Center for Emerging and Zoonotic Infectious Diseases (US), Centre Hospitalier de l’Université de Montréal (CA)
Good health and well-being
Openalex Percentile: Top 66%
Cervical Cancer and HPV Research
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