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

نویسندگان

  • Cheryl Cohen
  • Claire von Mollendorf
  • Linda de Gouveia
  • Nireshni Naidoo
  • Susan Meiring
  • Vanessa Quan
  • Vusi Nokeri
  • Melony Fortuin-de Smit
  • Babatyi Malope-Kgokong
  • David Moore
  • Gary Reubenson
  • Mamokgethi Moshe
  • Shabir A. Madhi
  • Brian Eley
  • Ute Hallbauer
  • Ranmini Kularatne
  • Laura Conklin
  • Katherine L. O'Brien
  • Elizabeth R. Zell
  • Keith Klugman
  • Cynthia G. Whitney
  • Anne von Gottberg
  • Charl Verwey
  • Sheeba Varughese
  • Moherndran Archary
  • Fathima Naby
  • Khathija Dawood
  • Ramola Naidoo
  • Gene Elliott
  • Ute Hallbauer
  • Brian Eley
  • James Nuttall
  • Louise Cooke
  • Heather Finlayson
  • Helena Rabie
  • Andrew Whitelaw
  • Dania Perez
  • Pieter Jooste
  • Dhamiran Naidoo
  • Ranmini Kularatne
  • Gary Reubenson
  • Cheryl Cohen
  • Linda de Gouveia
  • Mignon du Plessis
  • Nevashan Govender
  • Susan Meiring
  • Vanessa Quan
  • Claire von Mollendorf
  • Melony Fortuin-de Smidt
  • Nireshni Naidoo
  • Babatyi Malope-Kgokong
  • Vusi Nokeri
  • Relebohile Ncha
  • Sonwabo Lindani
  • Anne von Gottberg
  • Barry Spies
  • Lino Sono
  • Phasweni Maredi
  • Ken Hamese
  • Mamokgethi Moshe
  • Maphosane Nchabeleng
  • Ntombenhle Ngcobo
  • Johann van den Heever
  • Shabir Madhi
  • Laura Conklin
  • Jennifer Verani
  • Cynthia Whitney
  • Elizabeth Zell
  • Jennifer Loo
  • George Nelson
  • Keith Klugman
  • Katherine O'Brien
چکیده

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.

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عنوان ژورنال:

دوره 59  شماره 

صفحات  -

تاریخ انتشار 2014