Effect of childhood pneumococcal conjugate vaccination on invasive disease in older adults of 10 European countries: implications for adult vaccination.


Journal

Thorax
ISSN: 1468-3296
Titre abrégé: Thorax
Pays: England
ID NLM: 0417353

Informations de publication

Date de publication:
05 2019
Historique:
received: 14 03 2018
revised: 31 07 2018
accepted: 20 08 2018
pubmed: 26 10 2018
medline: 5 11 2019
entrez: 26 10 2018
Statut: ppublish

Résumé

Pneumococcal conjugate vaccines (PCVs) have the potential to prevent pneumococcal disease through direct and indirect protection. This multicentre European study estimated the indirect effects of 5-year childhood PCV10 and/or PCV13 programmes on invasive pneumococcal disease (IPD) in older adults across 13 sites in 10 European countries, to support decision-making on pneumococcal vaccination policies. For each site we calculated IPD incidence rate ratios (IRR) in people aged ≥65 years by serotype for each PCV10/13 year (2011-2015) compared with 2009 (pre-PCV10/13). We calculated pooled IRR and 95% CI using random-effects meta-analysis and PCV10/13 effect as (1 - IRR)*100. After five PCV10/13 years, the incidence of IPD caused by all types, PCV7 and additional PCV13 serotypes declined 9% (95% CI -4% to 19%), 77% (95% CI 67% to 84%) and 38% (95% CI 19% to 53%), respectively, while the incidence of non-PCV13 serotypes increased 63% (95% CI 39% to 91%). The incidence of serotypes included in PCV13 and not in PCV10 decreased 37% (95% CI 22% to 50%) in six PCV13 sites and increased by 50% (95% CI -8% to 146%) in the four sites using PCV10 (alone or with PCV13). In 2015, PCV13 serotypes represented 20-29% and 32-53% of IPD cases in PCV13 and PCV10 sites, respectively. Overall IPD incidence in older adults decreased moderately after five childhood PCV10/13 years in 13 European sites. Large declines in PCV10/13 serotype IPD, due to the indirect effect of childhood vaccination, were countered by increases in non-PCV13 IPD, but these declines varied according to the childhood vaccine used. Decision-making on pneumococcal vaccination for older adults must consider the indirect effects of childhood PCV programmes. Sustained monitoring of IPD epidemiology is imperative.

Sections du résumé

BACKGROUND
Pneumococcal conjugate vaccines (PCVs) have the potential to prevent pneumococcal disease through direct and indirect protection. This multicentre European study estimated the indirect effects of 5-year childhood PCV10 and/or PCV13 programmes on invasive pneumococcal disease (IPD) in older adults across 13 sites in 10 European countries, to support decision-making on pneumococcal vaccination policies.
METHODS
For each site we calculated IPD incidence rate ratios (IRR) in people aged ≥65 years by serotype for each PCV10/13 year (2011-2015) compared with 2009 (pre-PCV10/13). We calculated pooled IRR and 95% CI using random-effects meta-analysis and PCV10/13 effect as (1 - IRR)*100.
RESULTS
After five PCV10/13 years, the incidence of IPD caused by all types, PCV7 and additional PCV13 serotypes declined 9% (95% CI -4% to 19%), 77% (95% CI 67% to 84%) and 38% (95% CI 19% to 53%), respectively, while the incidence of non-PCV13 serotypes increased 63% (95% CI 39% to 91%). The incidence of serotypes included in PCV13 and not in PCV10 decreased 37% (95% CI 22% to 50%) in six PCV13 sites and increased by 50% (95% CI -8% to 146%) in the four sites using PCV10 (alone or with PCV13). In 2015, PCV13 serotypes represented 20-29% and 32-53% of IPD cases in PCV13 and PCV10 sites, respectively.
CONCLUSION
Overall IPD incidence in older adults decreased moderately after five childhood PCV10/13 years in 13 European sites. Large declines in PCV10/13 serotype IPD, due to the indirect effect of childhood vaccination, were countered by increases in non-PCV13 IPD, but these declines varied according to the childhood vaccine used. Decision-making on pneumococcal vaccination for older adults must consider the indirect effects of childhood PCV programmes. Sustained monitoring of IPD epidemiology is imperative.

Identifiants

pubmed: 30355641
pii: thoraxjnl-2018-211767
doi: 10.1136/thoraxjnl-2018-211767
pmc: PMC6484683
doi:

Substances chimiques

10-valent pneumococcal conjugate vaccine 0
Pneumococcal Vaccines 0

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

473-482

Investigateurs

Helena Sebestova (H)
Marek Maly (M)
Kurt Fuursted (K)
Tine Dalby (T)
Victoria F De Casadevante (VF)
Zitta Harboe (Z)
Charlotte Sværke Jørgensen (CS)
Sarah Collins (S)
Nick Andrews (N)
Abdelmajid Djennad (A)
Richard Pebody (R)
Jukka Jokinen (J)
Emmanuel Belchior (E)
Daniel Levy-Bruhl (D)
Scarlett Georges (S)
Marie-Cécile Ploy (MC)
Jacques Gaillat (J)
Robert Cunney (R)
Hilary Humphreys (H)
Suzanne Cotter (S)
Elisabeth Sanders (E)
Wim van der Hoek (WV)
Guy Berbers (G)
Hester de Melker (H)
Marianne Bergsaker (M)
Claire Cameron (C)
Barbara Denham (B)
Conchita Izquierdo (C)
Sonia Broner (S)
Roman Pallarés (R)
Luis Garcia (L)
Juan Carlos Sanz (JC)
Carmen Ezpeleta (C)
Alberto Gil-Setas (A)
Tiia Lepp (T)
Jessica Darenberg (J)
Edoardo Colzani (E)
Marta Valenciano (M)
Alain Moren (A)

Informations de copyright

© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: The following authors report funding for research projects, travels or consultancy outside the submitted work: H-CS (project sponsored by Pfizer); ZH (travel grant from Pfizer), SNL (research including GSK, Pfizer, Sanofi Pasteur on behalf of St George’s University of London and Public Health England (PHE)); NKF (employed by PHE Respiratory and Vaccine Preventable Bacteria Reference Unit and PHE Immunisation that provided serotype surveillance reports to Affinivax, Pfizer and GSK); HR-K and JJ (employed by the National Institute for Health and Welfare that received research funding from GSK for the conduct of a trial of PCV10); AvdE (Pfizer grant for an investigator initiated project, consultancy fees from GSK, participation in the Pfizer Scientific Advisory board); CM-A (fees from GSK and grants from Pfizer); EV (Pfizer grants and personal fees); MC (Pfizer grants and personal fees); HH (research funding from Pfizer and Astellas).

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Auteurs

Germaine Hanquet (G)

EpiConcept, Paris, France.
Antwerp University, Antwerp, Belgium.

Pavla Krizova (P)

National Institute of Public Health, Prague, Czech Republic.

Palle Valentiner-Branth (P)

Statens Serum Institut, Copenhagen, Denmark.

Shamez N Ladhani (SN)

Public Health England, London, UK.

J Pekka Nuorti (JP)

National Institute for Health and Welfare, Helsinki, Finland.
University of Tampere, Tampere, Finland.

Agnes Lepoutre (A)

Santé publique France, Saint-Maurice, France.

Jolita Mereckiene (J)

Health Protection Surveillance Centre, Dublin, Ireland.

Mirjam Knol (M)

National Institute for Public Health and the Environment, Bilthoven, The Netherlands.

Brita A Winje (BA)

Norwegian Institute of Public Health, Oslo, Norway.

Pilar Ciruela (P)

Public Health Agency of Catalunya, Barcelona, Spain.
CIBER Epidemiología y Salud Pública, Madrid, Spain.

Maria Ordobas (M)

General Directorate of Public Health, Madrid, Spain.

Marcela Guevara (M)

CIBER Epidemiología y Salud Pública, Madrid, Spain.
Instituto de Salud Pública de Navarra - IdiSNA, Pamplona, Spain.

Eisin McDonald (E)

Health Protection Scotland, National Services Scotland, Glasgow, UK.

Eva Morfeldt (E)

Public Health Agency of Sweden, Solna, Sweden.

Jana Kozakova (J)

National Institute of Public Health, Prague, Czech Republic.

Hans-Christian Slotved (HC)

Statens Serum Institut, Copenhagen, Denmark.

Norman K Fry (NK)

Public Health England, London, UK.

Hanna Rinta-Kokko (H)

National Institute for Health and Welfare, Helsinki, Finland.

Emmanuelle Varon (E)

National Centre for Pneumococci, European Hospital George Pompidou, Paris, France.

Mary Corcoran (M)

Irish Pneumococcal Reference Laboratory, Temple Street Children's University Hospital, Dublin, Ireland.

Arie van der Ende (A)

Netherlands Reference Laboratory for Bacterial Meningitis, Academic Medical Centre, Amsterdam, The Netherlands.

Didrik F Vestrheim (DF)

Norwegian Institute of Public Health, Oslo, Norway.

Carmen Munoz-Almagro (C)

CIBER Epidemiología y Salud Pública, Madrid, Spain.
Instituto de Recerca Pediátrica, Hospital Sant Joan de Deu, Universitat Internacional de Catalunya, Barcelona, Spain.

Pello Latasa (P)

General Directorate of Public Health, Madrid, Spain.

Jesus Castilla (J)

CIBER Epidemiología y Salud Pública, Madrid, Spain.
Instituto de Salud Pública de Navarra - IdiSNA, Pamplona, Spain.

Andrew Smith (A)

Scottish Haemophilus, Legionella, Meningococcus and Pneumococcus Reference Laboratory, Glasgow, UK.

Birgitta Henriques-Normark (B)

Public Health Agency of Sweden, Solna, Sweden.
Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Department of Clinical Microbiology, Karolinska University Hospital, Stockholm, Sweden.

Robert Whittaker (R)

European Centre for Disease Prevention and Control, Stockholm, Sweden.

Lucia Pastore Celentano (L)

European Centre for Disease Prevention and Control, Stockholm, Sweden.

Camelia Savulescu (C)

EpiConcept, Paris, France.

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