ABSTRACT
Introduction: Infections with oncogenic human papillomaviruses (HPV) globally cause about 9% of cancers in females and 1% of cancers in males. HPV disease burden can be effectively controlled by prophylactic HPV-vaccination provided it has high impact.
Areas covered: A unique series of biobank-based and health registry-based studies that exploit randomized intervention cohorts has provided data on population-level safety of HPV vaccination, duration of vaccine-induced protection and impact of gender-neutral HPV vaccination, providing a scientific basis for policies to eradicate oncogenic HPV types and associated diseases worldwide.
Expert commentary: The ultimate goal of HPV vaccination is the eradication of high-risk (hr) HPVs. Seventy-five percent coverage gender-neutral vaccination of early adolescents will rapidly eradicate also HPV16 from the general population.
Article highlights
Safety – Health registry-based follow up of both large scale randomized trials and HPV vaccination programs have found no evidence of increased occurrence of new onset autoimmune diseases of adverse pregnancy outcomes.
Immunogenicity – Resilience of antibody response post-vaccination has been described up to 15 years post-vaccination for all licensed HPV vaccines albeit with differences in the sustained antibody levels
Long-term efficacy – No HPV-associated cancer cases have been identified in cohorts vaccinated with the bivalent or the quadrivalent HPV vaccine while unvaccinated females have been diagnosed with a significantly higher incidence of HPV-associated cancers.
Impact of different vaccination strategies – A community-randomized trial shows that low to moderate coverage gender-neutral vaccination rapid establishes herd effect and overall protection against high-risk HPV types 18/31/33/35 but not against HPV16.
Eradication – State of the science mathematical models predict that eradication of high-risk HPV types is possible if the gender-neutral vaccination program has 70% coverage in both sexes.
Declaration of interest
The author has previously received grants for his HPV vaccination studies from Merck & Co. Inc. and GSK vaccines through his employer University of Tampere, Finland.
Reviewer disclosures
Peer reviewers on this manuscript have no relevant financial or other relationships to disclose.