Nasopharyngeal Carriage of Pneumococcus in Children in England up to 10 Years After 13-Valent Pneumococcal Conjugate Vaccine Introduction: Persistence of Serotypes 3 and 19A and Emergence of 7C

Author:

Tiley Karen S1ORCID,Ratcliffe Helen1,Voysey Merryn1ORCID,Jefferies Kimberley1,Sinclair Gemma1,Carr Melanie1,Colin-Jones Rachel1,Smith David1,Bowman Jaclyn1,Hart Thomas1,Kandasamy Rama1,Hinds Jason23,Gould Katherine23,Berbers Guy4,Tcherniaeva Irina4,Robinson Hannah156,Plested Emma156,Aley Parvinder15,Snape Matthew D15

Affiliation:

1. Oxford Vaccine Group, Department of Paediatrics, University of Oxford , Oxford , United Kingdom

2. Institute for Infection and Immunity, St George’s University , London , United Kingdom

3. BUGS Bioscience, London Bioscience Innovation Centre , London , United Kingdom

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

5. National Institute for Health Research Oxford Biomedical Research Centre , Oxford , United Kingdom, and

6. National Institute for Health Research Clinical Research Network Thames Valley and South Midlands , Oxford , United Kingdom

Abstract

Abstract Background Monitoring changes in pharyngeal carriage of pneumococcus in children following 13-valent pneumococcal conjugate vaccine (PCV13) introduction in the United Kingdom in 2010 informs understanding of patterns of invasive pneumococcal disease (IPD) incidence. Methods Nasopharyngeal swabs from healthy children vaccinated with PCV13 according to schedule (2, 4, and 12 months) were cultured and serotyped. Results for children aged 13–48 months were compared between 2014–2015 and 2017–2019 and with children aged 6–12 months (2017–2020). Blood was obtained from a subset of children for pneumococcal serotype-specific immunoglobulin G (IgG). Results Total pneumococcal carriage at 13–48 months was 47.9% (473/988) in 2014–2015 and 51.8% (412/795) in 2017–2019 (P = .10); at age 6–12 months this value was 44.6% (274/615). In 2017–2019, 2.9% (95% confidence interval, 1.8%–4.3%) of children aged 13–48 months carried PCV13 serotypes (mainly 3 [1.5%] and 19A [0.8%]) and >20% carried the additional 20-valent PCV (PCV20) serotypes. Similar proportions of children had IgG ≥0.35 IU/mL for each serotype in 2014–2015 and 2017–2019. Serotype 7C carriage increased significantly (P < .01) between 2014–2015 and 2017–2019. Carriage of PCV20 serotypes 8 and 12F, both major causes of IPD, was rare. Conclusions Introduction of PCV20, if licensed for children, could significantly change the composition of pneumococcal serotypes carried in the pharynx of UK children. Clinical Trials Registration NCT03102840.

Funder

Pfizer

University of Oxford

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

Reference37 articles.

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