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Author Notes:

Corresponding Author : Cheryl Cohen, MB, BCh, MSc, Centre for Respiratory Diseases and Meningitis, National Institute for Communicable Diseases, Private Bag X4, Sandringham, 2131, Johannesburg, South Africa (cherylc@nicd.ac.za).

We thank all the participants and their caregivers who kindly agreed to be included in this study; Group for Enteric, Respiratory and Meningeal pathogens Surveillance - South Africa surveillance officers for their tireless efforts to enroll participants and to obtain vaccination histories; laboratory staff throughout the country for submitting isolates to the National Institute for Communicable Diseases (NICD); and the staff at the NICD, Centre for Respiratory Diseases and Meningitis laboratory for their efforts in processing and characterizing these isolates.

All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Subjects:

Research Funding:

This work was supported by GAVI through PATH

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Immunology
  • Infectious Diseases
  • Microbiology
  • children
  • HIV
  • pneumococcus
  • pneumococcal conjugate vaccine
  • South Africa
  • IMMUNIZATION PROGRAM
  • INFANTS
  • IMMUNOGENICITY
  • TRIAL
  • 1ST
  • METAANALYSIS
  • SCHEDULES
  • EFFICACY
  • IMPACT

Effectiveness of 7-Valent Pneumococcal Conjugate Vaccine Against Invasive Pneumococcal Disease in HIV-Infected and -Uninfected Children in South Africa: A Matched Case-Control Study

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Journal Title:

Clinical Infectious Diseases

Volume:

Volume 59, Number 6

Publisher:

, Pages 808-818

Type of Work:

Article | Final Publisher PDF

Abstract:

Background. South Africa introduced 7-valent pneumococcal conjugate vaccine (PCV7) in April 2009 using a 2 + 1 schedule (6 and 14 weeks and 9 months). We estimated the effectiveness of ≥2 PCV7 doses against invasive pneumococcal disease (IPD) in human immunodeficiency virus (HIV)- infected and -uninfected children. Methods. IPD (pneumococcus identified from a normally sterile site) cases were identified through national laboratory-based surveillance. Specimens were serotyped by Quellung or polymerase chain reaction. Four controls, matched for age, HIV status, and hospital were sought for each case. Using conditional logistic regression, we calculated vaccine effectiveness (VE) as 1 minus the adjusted odds ratio for vaccination. Results. From March 2010 through November 2012, we enrolled 187 HIV-uninfected (48 [26%] vaccine serotype) and 109 HIV-infected (43 [39%] vaccine serotype) cases and 752 HIV-uninfected and 347 HIV-infected controls aged ≥16 weeks. Effectiveness of ≥2 PCV7 doses against vaccine-serotype IPD was 74% (95% confidence interval [CI], 25%-91%) among HIV-uninfected and -12% (95% CI, -449% to 77%) among HIV-infected children. Effectiveness of ≥3 doses against vaccine-serotype IPD was 90% (95% CI, 14%-99%) among HIV-uninfected and 57% (95% CI, -371% to 96%) among HIV-infected children. Among HIV-exposed but -uninfected children, effectiveness of ≥2 doses was 92% (95% CI, 47%-99%) against vaccine-serotype IPD. Effectiveness of ≥2 doses against all-serotype multidrug-resistant IPD was 96% (95% CI, 62%-100%) among HIV-uninfected children. Conclusions. A 2 + 1 PCV7 schedule was effective in preventing vaccine-serotype IPD in HIV-uninfected and HIV-exposed, uninfected children. This finding supports the World Health Organization recommendation for this schedule as an alternative to a 3-dose primary series among HIV-uninfected individuals.

Copyright information:

© The Author 2014. Published by Oxford University Press on behalf of the Infectious.

This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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