Durability of the neutralizing antibody response to vaccine and non-vaccine HPV types 7 years following immunization with either Cervarix® or Gardasil® vaccine.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
24 04 2019
Historique:
received: 03 01 2019
revised: 08 03 2019
accepted: 22 03 2019
pubmed: 31 3 2019
medline: 17 9 2020
entrez: 31 3 2019
Statut: ppublish

Résumé

Bivalent (Cervarix®) and quadrivalent (Gardasil®) Human Papillomavirus (HPV) vaccines demonstrate remarkable efficacy against the targeted genotypes, HPV16 and HPV18, but also a degree of cross-protection against non-vaccine incorporated genotypes, HPV31 and HPV45. These outcomes seem to be supported by observations that the HPV vaccines induce high titer neutralizing antibodies against vaccine types and lower responses against non-vaccine types. Few data are available on the robustness of the immune response against non-vaccine types. We examined the durability of vaccine and non-vaccine antibody responses in a follow up of a head-to-head study of 12-15 year old girls initially randomized to receive three doses of Cervarix® or Gardasil® vaccine. Neutralizing antibodies against both vaccine and non-vaccine types remained detectable up to 7 years following initial vaccination and a mixed effects model was used to predict the decline in antibody titers over a 15 year period. The decline in vaccine and non-vaccine type neutralizing antibody titers over the study period was estimated to be 30% every 5-7 years, with Cervarix® antibody titers expected to remain 3-4 fold higher than Gardasil® antibody titers over the long term. The antibody decline rates in those with an initial response to non-vaccine types were similar to that of vaccine types and are predicted to remain detectable for many years. Empirical data on the breadth, magnitude, specificity and durability of the immune response elicited by the HPV vaccines contribute to improving the evidence base supporting this important public health intervention. Original trial: ClinicalTrials.gov NCT00956553.

Identifiants

pubmed: 30926298
pii: S0264-410X(19)30386-X
doi: 10.1016/j.vaccine.2019.03.052
pii:
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0
Human Papillomavirus Recombinant Vaccine Quadrivalent, Types 6, 11, 16, 18 0
Papillomavirus Vaccines 0
human papillomavirus vaccine, L1 type 16, 18 0

Banques de données

ClinicalTrials.gov
['NCT00956553']

Types de publication

Clinical Trial, Phase IV Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2455-2462

Subventions

Organisme : Department of Health
Pays : United Kingdom

Informations de copyright

Crown Copyright © 2019. Published by Elsevier Ltd. All rights reserved.

Auteurs

Anna Godi (A)

Virus Reference Department, Public Health England, London, UK.

Kavita Panwar (K)

Virus Reference Department, Public Health England, London, UK.

Mahmoud Haque (M)

Virus Reference Department, Public Health England, London, UK.

Clementina E Cocuzza (CE)

Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.

Nick Andrews (N)

Statistics, Modelling and Economics Department, Public Health England, London, UK.

Jo Southern (J)

Immunisation and Countermeasures Public Health England, London, UK.

Paul Turner (P)

Section of Paediatrics, Imperial College London, London, UK.

Elizabeth Miller (E)

Immunisation and Countermeasures Public Health England, London, UK.

Simon Beddows (S)

Virus Reference Department, Public Health England, London, UK. Electronic address: simon.beddows@phe.gov.uk.

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Classifications MeSH