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Three-year follow-up of 2-dose versus 3-dose HPV vaccine

  • Jacob Bornstein
  • , Surita Roux
  • , Lone Kjeld Petersen
  • , Li Min Huang
  • , Simon R. Dobson
  • , Punnee Pitisuttithum
  • , Javier Diez-Domingo
  • , Andrea Schilling
  • , Hany Ariffin
  • , Richard Tytus
  • , Richard Rupp
  • , Shelly Senders
  • , Eli Engel
  • , Daron Ferris
  • , Yae Jean Kim
  • , Young Tae Kim
  • , Zafer Kurugol
  • , Oliver Bautista
  • , Katrina M. Nolan
  • , Sandhya Sankaranarayanan
  • Alfred Saah, Alain Luxembourg
  • Synexus Clinical Research SA
  • University of Southern Denmark
  • National Taiwan University
  • University of British Columbia
  • Mahidol University
  • Foundation for the Promotion of Health and Biomedical Research of Valencia Region - Public Health
  • Clínica Alemana de Santiago
  • University of Malaya
  • Hamilton Medical Research Group
  • University of Texas Medical Branch at Galveston
  • Senders Pediatrics
  • Bayview Research Group
  • Augusta University
  • Samsung Medical Center, Sungkyunkwan university
  • Yonsei University
  • Ege University
  • Merck

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

BACKGROUND AND OBJECTIVES: Human papillomavirus (HPV) antibody responses to the 9-valent human papillomavirus (9vHPV) vaccine among girls and boys (aged 9-14 years) receiving 2-dose regimens (months 0, 6 or 0, 12) were noninferior to a 3-dose regimen (months 0, 2, 6) in young women (aged 16-26 years) 4 weeks after last vaccination in an international, randomized, open-label trial (NCT01984697). We assessed response durability through month 36. METHODS: Girls received 2 (months 0 and 6 [0, 6]: n = 301; months 0 and 12 [0, 12]: n = 151) or 3 doses (months 0,2, and 6 [0, 2, 6]: n = 301); boys received 2 doses ([0, 6]: n = 301; [0, 12]: n = 150); and young women received 3 doses ([0, 2, 6]: n = 314) of 9vHPV vaccine. Anti-HPV geometric mean titers (GMTs) were assessed by competitive Luminex immunoassay (cLIA) and immunoglobulin G-Luminex immunoassay (IgG-LIA) through month 36. RESULTS: Anti-HPV GMTs were highest 1 month after the last 9vHPV vaccine regimen dose, decreased sharply during the subsequent 12 months, and then decreased more slowly. GMTs 2 to 2.5 years after the last regimen dose in girls and boys given 2 doses were generally similar to or greater than GMTs in young women given 3 doses. Across HPV types, most boys and girls who received 2 doses (cLIA: 81%-100%; IgG-LIA: 91%-100%) and young women who received 3 doses (cLIA: 78%-98%; IgG-LIA: 91%-100%) remained seropositive 2 to 2.5 years after the last regimen dose. CONCLUSIONS: Antibody responses persisted through 2 to 2.5 years after the last dose of a 2-dose 9vHPV vaccine regimen in girls and boys. In girls and boys, antibody responses generated by 2 doses administered 6 to 12 months apart may be sufficient to induce high-level protective efficacy through at least 2 years after the second dose.

Original languageEnglish
Article numbere20194035
JournalPediatrics
Volume147
Issue number1
DOIs
StatePublished - 1 Jan 2021

Bibliographical note

Publisher Copyright:
Copyright © 2021 by the American Academy of Pediatrics

Funding

We thank the study participants, site personnel, and investigators; Michael Ritter and Sonali Rawat from Merck & Co, Inc, Kenilworth, NJ for their expert assistance in the scientific conduct of the study; Thomas Group from Merck Sharp & Dohme Corp for facilitating the immunologic testing of serum samples; and Xiaofei Hu from Merck Sharp & Dohme Corp for providing statistical expertise. Medical writing support, under the direction of the authors, was provided by Erin Bekes, PhD, of CMC AFFINITY, a division of McCann Health Medical Communications, Inc, funded by Merck Sharp & Dohme Corp, a subsidiary of Merck & Co, Inc, in accordance with Good Publication Practice guidelines.

Funders
Merck Sharp and Dohme
Catholic Medical Center

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

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