Benefits of the intervention
Serogroup or serotype coverage by vaccines considered (for serogroup- or serotype-specific vaccines)

The vaccines currently available provide protection vs. 6, 11, 16, 18, 31, 33, 45, 52, and 58 (type 6 and 11 are responsible for most anogenital warts). Go to footnote 1
Both Bivalent and Quadrivalent Vaccines show cross-protection, with the bivalent vaccine (targeting HPV-16/18) generally provides stronger and more consistent cross-protection, particularly against HPV-31, HPV-33, and HPV-45. Some studies also report partial protection against HPV-35, HPV-52, and HPV-58, though the evidence is less robust and more variable. Go to footnote 2

Efficacy and effectiveness estimates (e.g. against infection, disease, hospitalization, death), including in different populations

Meta-analysis: Three doses of the bivalent (Cervarix) and quadri-valent (Gardasil) vaccines offered significant protection against cervical adenocarcinoma in situ associated with HPV16 and HPV18 among young women (aged 15–26 years): 88% (95%CI 30–98%). Trials among vaccine recipients not already infected with HPV showed high efficacy against high-grade cervical, vulvar and vaginal lesions: 98% (95%CI 93–100) for CIN2+ and 100% (95%CI 83–100) for vulvar and vaginal intraepithelial neoplasia grade 2+ caused by the HPV types in the quadrivalent vaccine. Approval of the 2-dose schedule was based on demonstration of non-inferiority of the immune response when compared with young adult women (16-26 years of age) in whom 3-dose efficacy has been proven (immunobridging). A one-dose schedule is supported by WHO given that post-hoc analyses of efficacy trials, and post-licensure observational studies among African females (15-20 years of age) have demonstrated that a single dose of HPV vaccine is sufficient to elicit an immune response that provides similar protection as a multidose regimen against initial and persistent HPV infection.

Duration of protection and waning of immunity in general and risk groups

With a multidose schedule, antibody titres remain high for up to 12 years for the bivalent (Cervarix) vaccine for girls vaccinated at age 16-17, up to 15 years for quadrivalent (Gardasil) vaccine, and for at least 6 years for the more recently licensed nonavalent vaccine (Gardasil-9). Go to footnote 3, Go to footnote 4, Go to footnote 5  GMT following a single dose remain stable through at least 10-16 years.  Go to footnote 6, Go to footnote 7 

Sources
  • Go back to footnote reference 1

    HPV vaccines: WHO position paper (https://www.who.int/publications/i/item/who-wer9750-645-672)
    Demarco M et al. EClinicalMedicine. 2020, 22:100293

  • Go back to footnote reference 2

    Tsang, S., Sampson, J., Schussler, J., Porras, C., Wagner, S., Boland, J., Cortés, B., Lowy, D., Schiller, J., Schiffman, M., Kemp, T., Rodriguez, A., Quint, W., Gail, M., Pinto, L., González, P., Hildesheim, A., Kreimer, A., & Herrero, R. (2020). Durability of Cross-Protection by Different Schedules of the Bivalent HPV Vaccine: the CVT Trial.. Journal of the National Cancer Institute. https://doi.org/10.1093/jnci/djaa010

  • Go back to footnote reference 3

    World Health Organization (2022). Human papillomavirus vaccines: WHO position paper – December 2022. Wkly Epidemiol Rec. 97(50):645–672 (https://iris.who.int/bitstream/handle/10665/365350/WER9750-eng-fre.pdf?sequence=1, accessed 19 June 2025).

  • Go back to footnote reference 4

    Olsson S-E, Van Damme P, Block SL, Castellsagué X, Gray GE, Herrera T et al. (2020). Long-term immunogenicity, effectiveness, and safety of nine-valent human papillomavirus vaccine in girls and boys 9 to 15 years of age: interim analysis after 8 years of follow-up. Papillomavirus Res. 10:100203. doi:10.1016/j.pvr.2020.100203.

  • Go back to footnote reference 5

    Malvi, S.G., Esmy, P.O., Muwonge, R., Joshi, S., Poli, U.R.R., et al, 2024. A prospective cohort study comparing efficacy of 1 dose of quadrivalent human papillomavirus vaccine to 2 and 3 doses at an average follow up of 12 years postvaccination. J Natl Cancer Inst Monogr 2024, 317–328. https://doi.org/10.1093/jncimonographs/lgae042

  • Go back to footnote reference 6

    Restrepo J, Scherer EM, Smith RA, Gallego DF, Carter JJ, Wipf GC et al. (2023). Ten-year follow-up of 9-valent human papillomavirus vaccine: immunogenicity, effectiveness, and safety. Pediatrics. 152:e2022060993. doi:10.1542/peds.2022-060993.

  • Go back to footnote reference 7

    Porras, C., Romero, B., Kemp, T., Fantin, R., Herrero, R., et al. Costa Rica HPV Vaccine Trial Study Group, 2024. HPV16/18 antibodies 16-years after single dose of bivalent HPV vaccination: Costa Rica HPV vaccine trial. J Natl Cancer Inst Monogr 2024, 329–336. https://doi.org/10.1093/jncimonographs/lgae032

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