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Immunization of Early Adolescent Females with Human Papillomavirus Type 16 and 18 L1 Virus-Like Particle Vaccine Containing AS04 Adjuvant
Authors:Court Pedersen M.D.   Sc.D.   Tiina Petaja M.D.   Gitte Strauss M.D.   Hans C. Rumke M.D.   Airi Poder M.D.   Jan Hendrik Richardus M.D.   Ph.D.   Bart Spiessens Ph.D.   Dominique Descamps M.D.   Karin Hardt Ph.D.   Matti Lehtinen M.D.   Ph.D.   Gary Dubin M.D.  HPV Vaccine Adolescent Study Investigators Network
Affiliation:

aOdense University Hospital, Odense, Denmark

bUniversity of Tampere, School of Public Health, Tampere, Finland

cBispebjerg hospital, Department of Dermato-venerology, Copenhagen, Denmark

dVaxinostics BV, University Vaccine Center, Rotterdam, The Netherlands

eTartu University Clinics, Dermatology, Tartu, Estonia

fMunicipal Public Health Service Rotterdam Area, Infectious Disease Control Rotterdam, Rotterdam, The Netherlands

gGlaxoSmithKline Biologicals, Rixensart, Belgium

hGlaxoSmithKline Biologicals, King of Prussia, Pennsylvania

Abstract:
PurposeIn female individuals 15–25-years of age, the AS04-containing human papillomavirus (HPV)–16/18 vaccine is highly immunogenic and provides up to 100% protection against HPV-16/18 persistent infection and associated cervical lesions up to 4.5 years. Optimal cervical cancer prevention will require prophylactic vaccination against oncogenic HPV 16 and 18 before the onset of sexual activity in early adolescent girls. To establish the feasibility of vaccination in girls 10–14 years of age, we compared the immunogenicity and safety in early adolescent female individuals to those 15–25 years in whom vaccine efficacy has been demonstrated.MethodsWe enrolled 773 female participants aged 10–14 years and 15–25 years to receive the HPV-16/18 L1 VLP AS04 vaccine, which was administered at months 0, 1, and 6. Serum samples were collected at months 0 and 7; antibodies to HPV 16 and 18 VLPs were measured by enzyme-linked immunosorbent assay. Vaccine safety was assessed at 7 or 30 days after each dose; serious adverse events were recorded during the entire study period.ResultsBoth age groups achieved 100% seroconversion for HPV 16 and 18. Participants in the group aged 10–14 years were not only noninferior to those 15–25 years in terms of HPV 16 and 18 seroconversion rates but also had approximately twice as high geometric mean titers. The vaccine was generally safe and well tolerated.ConclusionsThese findings suggest that HPV vaccination during early adolescence is generally safe, well tolerated, and highly immunogenic. The observed higher antibody titers in the group 10–14 years of age are likely to result in longer antibody persistence. Overall, these data support the implementation of prophylactic HPV vaccination in this age group.
Keywords:Human papillomavirus vaccine   Cervical cancer   Immunogenicity   AS04   Adolescent   Female
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