Efficacy and immunogenicity of a single dose of human papillomavirus vaccine compared to no vaccination or standard three and two-dose vaccination regimens: A systematic review of evidence from clinical trials.


Journal

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

Informations de publication

Date de publication:
05 02 2020
Historique:
received: 13 08 2019
revised: 04 12 2019
accepted: 07 12 2019
pubmed: 25 12 2019
medline: 9 3 2021
entrez: 25 12 2019
Statut: ppublish

Résumé

This study aimed to systematically review the literature on the efficacy and immunogenicity of single-dose HPV vaccination compared to no vaccination or multi-dose schedules among vaccine trial participants. Medline, EMBASE, Global Health Database and Cochrane Central Register of Controlled Trials were searched for publications and conference abstracts (dated January 1999-August 2018) using MeSH and non-MeSH terms for human papillomavirus AND vaccines AND (immunogenicity OR efficacy/effectiveness) AND dosage. Search results were screened against pre-specified eligibility criteria. Data were extracted from included articles, and a narrative synthesis conducted on efficacy against HPV16/18 infection and humoral immunogenicity. Seven of 6,523 unique records identified were included in the review. Six were nested observational studies of participants randomised to receive two or three doses in three large HPV vaccine trials, in which some participants did not complete their allocated schedules. One small pilot study prospectively allocated participants to receive one or no vaccine dose. Frequency of HPV16/18 infection was low (e.g. <1% for 12-month-persistent infection) in all vaccinated participants up to seven years post vaccination and did not significantly differ by number of doses (p > 0.05 in all cases). Frequency of infection was significantly lower in one-dose recipients compared to unvaccinated controls (p < 0.01 for all infection endpoints in each study). HPV16/18 seropositivity rates were high in all HPV vaccine recipients (100% in three of four studies reporting this endpoint), though antibody levels were lower with one compared to two or three doses. This review supports the premise that one HPV vaccine dose may be as effective in preventing HPV infection as multi-dose schedules in healthy young women. However, it also highlights the paucity of available evidence from purpose-designed, prospectively-randomised trials. Results from ongoing clinical trials assessing the efficacy and immunogenicity of single-dose HPV vaccination compared to currently-recommended schedules are awaited.

Identifiants

pubmed: 31870572
pii: S0264-410X(19)31659-7
doi: 10.1016/j.vaccine.2019.12.017
pii:
doi:

Substances chimiques

Papillomavirus Vaccines 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1302-1314

Informations de copyright

Copyright © 2019. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Hilary S Whitworth (HS)

Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom; Mwanza Intervention Trials Unit, National Institute of Medical Research, Mwanza, Tanzania. Electronic address: hilary.whitworth@lshtm.ac.uk.

Katherine E Gallagher (KE)

Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Natasha Howard (N)

Faculty of Public Health and Policy, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Sandra Mounier-Jack (S)

Faculty of Public Health and Policy, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Gladys Mbwanji (G)

Mwanza Intervention Trials Unit, National Institute of Medical Research, Mwanza, Tanzania.

Aimée R Kreimer (AR)

National Cancer Institute, National Institute of Health, Bethesda, MD, United States.

Partha Basu (P)

International Agency for Research on Cancer, World Health Organization, Lyon, France.

Helen Kelly (H)

Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Mélanie Drolet (M)

Centre de recherche du CHU de Québec, Université Laval, Quebec, Canada.

Marc Brisson (M)

Centre de recherche du CHU de Québec, Université Laval, Quebec, Canada; Department of Social and Preventive Medicine, Laval University, Québec, Canada.

Deborah Watson-Jones (D)

Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom; Mwanza Intervention Trials Unit, National Institute of Medical Research, Mwanza, Tanzania.

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Classifications MeSH