Effect on nasopharyngeal pneumococcal carriage of replacing PCV7 with PCV13 in the Expanded Programme of Immunization in The Gambia

  • Anna Roca
  • , Abdoulie Bojang
  • , Christian Bottomley
  • , Rebecca A. Gladstone
  • , Jane U. Adetifa
  • , Uzochukwu Egere
  • , Sarah Burr
  • , Martin Antonio
  • , Stephen Bentley
  • , Beate Kampmann
  • , Claire Oluwalana
  • , Olubukola Idoko
  • , Isatou Cox
  • , Brenda Kwambana
  • , Sheikh Jarju
  • , Ebenezer Foster-Nyarko
  • , Brian Greenwood

Research output: Contribution to journalArticlepeer-review

46 Citations (Scopus)

Abstract

Introduction: In 2011, two years after the introduction of 7-valent Pneumococcal conjugate vaccine (PCV7), the Gambian immunization programme replaced PVC7 with PCV13 (13-valent). Our objective was to assess the additional impact of PCV13 on prevalence of pneumococcal nasopharyngeal carriage. Methods: We recruited healthy Gambian infants who had received three PCV doses. Nasopharyngeal swabs were collected from infants and their mothers during two cross-sectional surveys (CSS) conducted in infants vaccinated with PCV7 (CSS1) and vaccinated with PCV13 (CSS2). Pneumococci were isolated and serotyped following standardized methods. Whole genome sequencing was performed on non-typable pneumococcus isolated in CSS1 and CSS2. Results: 339 and 350 infants and their mothers were recruited in CSS1 and CSS2, respectively. Overall prevalence of pneumococcal carriage was 85.4% in infants. Among infants, prevalence of vaccine type (VT) carriage was lower in CSS2 [9.4% versus 4.9% (p= 0.025) for PCV7-VT; 33.3% versus 18.3% (p< 0.001) for PCV13-VT and 23.9% versus 13.7% (p= 0.001) for the 6 additional serotypes included in PCV13]. At CSS2, there was a decrease of serotypes 6A (from 15.3% to 5.7%, p< 0.001) and 19F (from 5.6% to 1.7%, p= 0.007), and an increase of non-typable pneumococci (0.3-6.0%, p< 0.001), most of which (82.4%) were from typable serotype backgrounds that had lost the ability to express a capsule. Prevalence of overall and VT carriage in mothers was similar in CSS1 and CSS2. Conclusions: Replacing PCV7 for PCV13 rapidly decreased prevalence of VT carriage among vaccinated Gambian infants. An indirect effect in mothers was not observed yet. Vaccine-driven selection pressure may have been responsible for the increase of non-typable isolates.
Original languageEnglish
Pages (from-to)7144-7151
Number of pages8
JournalVaccine
Volume33
Issue number51
DOIs
Publication statusPublished - 16 Dec 2015
Externally publishedYes

Keywords

  • Africa
  • Epidemiology
  • Expanded Programme of Immunization
  • Non-typable
  • PCV13
  • PCV7
  • Vaccine-type

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