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Pneumococcal carriage in vaccine-eligible children and unvaccinated infants in Lao PDR two years following the introduction of the 13-valent pneumococcal conjugate vaccine

Authors :
Jason Hinds
Anonh Xeuatvongsa
Kimberley Fox
Belinda D. Ortika
Monica L Nation
Eleanor F. G. Neal
Catherine Satzke
Eileen M. Dunne
Katherine A. Gould
Fiona M. Russell
E. Kim Mulholland
Casey L Pell
Vanphanom Sychareun
Anisone Chanthongthip
Molina Choummanivong
Cattram D. Nguyen
Source :
Vaccine. 37:296-305
Publication Year :
2019
Publisher :
Elsevier BV, 2019.

Abstract

Pneumococcal carriage is a prerequisite for disease, and underpins herd protection provided by pneumococcal conjugate vaccines (PCVs). There are few data on the impact of PCVs in lower income settings, particularly in Asia. In 2013, the Lao People's Democratic Republic (Lao PDR) introduced 13-valent PCV (PCV13) as a 3 + 0 schedule (doses at 6, 10 and 14 weeks of age) with limited catch-up vaccination. We conducted two cross-sectional carriage surveys (pre- and two years post-PCV) to assess the impact of PCV13 on nasopharyngeal pneumococcal carriage in 5-8 week old infants (n = 1000) and 12-23 month old children (n = 1010). Pneumococci were detected by quantitative real-time PCR, and molecular serotyping was performed using DNA microarray. Post PCV13, there was a 23% relative reduction in PCV13-type carriage in children aged 12-23 months (adjusted prevalence ratio [aPR] 0.77 [0.61-0.96]), and no significant change in non-PCV13 serotype carriage (aPR 1.11 [0.89-1.38]). In infants too young to be vaccinated, there was no significant change in carriage of PCV13 serotypes (aPR 0.74 [0.43-1.27]) or non-PCV13 serotypes (aPR 1.29 [0.85-1.96]), although trends were suggestive of indirect effects. Over 70% of pneumococcal-positive samples contained at least one antimicrobial resistance gene, which were more common in PCV13 serotypes (p

Details

ISSN :
0264410X and 18732518
Volume :
37
Database :
OpenAIRE
Journal :
Vaccine
Accession number :
edsair.doi.dedup.....5152e84ea9935bdbfa4b861cf36dd5d1
Full Text :
https://doi.org/10.1016/j.vaccine.2018.10.077