Journal of Adolescent Health
Volume 50, Issue 2 , Pages 187-194, February 2012

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

  • Tino F. Schwarz, M.D.

      Affiliations

    • Central Laboratory and Vaccination Centre, Stiftung Juliusspital Wuerzburg, Wuerzburg, Germany
    • Corresponding Author InformationAddress correspondence to: Tino F. Schwarz, M.D., Zentrallabor, Stiftung Juliusspital, Juliuspromenade 19, D-97070 Würzburg, Germany
  • ,
  • Li-Min Huang, M.D., Ph.D.

      Affiliations

    • Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan
  • ,
  • Doris Maribel Rivera Medina, M.D.

      Affiliations

    • Organización para el Desarrollo y la Investigación Salud en Honduras, Tegucigalpa, Honduras
  • ,
  • Alejandra Valencia, M.D.

      Affiliations

    • Fundación Santa Fe de Bogotá, Bogota, Colombia
  • ,
  • Tzou-Yien Lin, M.D.

      Affiliations

    • Chang-Gung Memorial Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan
    • Chang Gung Children's Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan
  • ,
  • Ulrich Behre, M.D.

      Affiliations

    • Pediatric Practice Kehl, Kehl, Germany
  • ,
  • Grégory Catteau, M.Sc.

      Affiliations

    • GlaxoSmithKline Biologicals, Wavre, Belgium
  • ,
  • Florence Thomas, M.D.

      Affiliations

    • GlaxoSmithKline Biologicals, Wavre, Belgium
  • ,
  • Dominique Descamps, M.D.

      Affiliations

    • GlaxoSmithKline Biologicals, Wavre, Belgium

Received 21 June 2011; accepted 4 November 2011.

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

Journal of Adolescent Health
Volume 50, Issue 2 , Pages 187-194, February 2012