Four-Year Follow-up of the Immunogenicity and Safety of the HPV-16/18 AS04-Adjuvanted Vaccine When Administered to Adolescent Girls Aged 10–14 Years
Abstract
Purpose
Long-term immunogenicity and safety of the human papillomavirus (HPV)-16/18 AS04-adjuvanted vaccine when administered to adolescent girls was evaluated.
Methods
This open-label, follow-up study (NCT00316706) was conducted in 31 centers in Taiwan, Germany, Honduras, Panama, and Colombia. In the initial study (NCT00196924), 1,035 girls aged 10–14 years received the HPV-16/18 AS04-adjuvanted vaccine at 0, 1, and 6 months. Here, geometric mean titers (GMTs) of antibodies against HPV-16, HPV-18, and monophosphoryl lipid A (MPL), a component of the AS04 Adjuvant System, were reported up to month 48.
Results
In the according-to-protocol immunogenicity cohort (N = 563), GMTs at month 48 in initially seronegative participants were 2,374.9 (95% confidence interval: 2,205.7–2,557.0) EL.U/mL for anti-HPV-16 and 864.8 (796.9–938.4) EL.U/mL for anti-HPV-18, that is, six- and threefold higher than the plateau level in a reference study demonstrating vaccine efficacy in young women (age, 15–25 years). All participants remained seropositive for anti-HPV-16 and anti-HPV-18 at month 48. Most participants (81.8%) were seropositive for anti-MPL antibodies before vaccination. Anti-MPL antibody titers in initially seropositive participants increased initially, and then declined. Most initially seronegative participants for anti-MPL seroconverted; 69.6% remained seropositive at month 48, with anti-MPL antibody titers similar to the natural background level. The vaccine was generally well tolerated. No serious adverse events were considered related to vaccination.
Conclusions
In adolescent girls, the HPV-16/18 AS04-adjuvanted vaccine produces anti-HPV-16 and anti-HPV-18 antibody titers that are maintained for up to 4 years at higher levels than those in young women in whom vaccine efficacy against cervical lesions was demonstrated.
Keywords: Human papillomavirus , Cervical cancer , HPV-16/18 AS04-adjuvanted vaccine , Immunogenicity , Safety , Monophosphoryl lipid A , Long-term , Adolescent , Female
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All authors have completed the Unified Competing Interest form at http://www.icmje.org/coi_disclosure.pdf and declare that the institutions of Doris Maribel Rivera Medina and L.M. Huang had received grant from GlaxoSmithKline Biologicals; T.F. Schwarz and L.M. Huang received board membership, consulting fees, and support for travel from GlaxoSmithKline Biologicals; T.F. Schwarz also received payment for lectures by GlaxoSmithKline Biologicals; A. Valencia received consulting fees and payments for travels and for the development of educational presentations from GlaxoSmithKline Biologicals and Abbott International; G. Catteau, F. Thomas, and D. Descamps are employees of GlaxoSmithKline Biologicals, and F. Thomas and D. Descamps hold stock options from GlaxoSmithKline Biologicals.
Trial registration number: NCT00316706 (http://www.clinicaltrials.gov).
PII: S1054-139X(11)00615-X
doi:10.1016/j.jadohealth.2011.11.004
© 2012 Published by Elsevier Inc.
