AI Article Synopsis

  • - The introduction of pneumococcal conjugate vaccines (PCVs) in children has significantly reduced pneumococcal disease globally, with two main types being PHiD-CV and PCV13.
  • - Although these vaccines differ in some serotype compositions, their overall impact on reducing disease burden in children is similar, suggesting that the presence of different serotypes doesn't always lead to different outcomes.
  • - PHiD-CV lacks protection against serotype 3, while PCV13 shows inconsistent results against it; both vaccines lead to some replacement of vaccine-targeted serotypes with non-vaccine strains, ultimately resulting in similar levels of overall disease burden.

Article Abstract

The worldwide implementation of pneumococcal conjugate vaccines (PCVs) in children has reduced the overall pneumococcal disease burden. Two PCVs are widely available for infant vaccination: the pneumococcal non-typeable protein D conjugate vaccine (PHiD-CV) and the 13-valent PCV (PCV13). While these PCVs differ in serotype composition (PCV13 includes polysaccharides of serotypes 3, 6A and 19A; PHiD-CV does not), their impact on the overall pneumococcal disease burden in children is comparable. This commentary summarizes the evidence of comparability between PHiD-CV and PCV13 and explores why differences in serotype composition may not necessarily translate into a differential clinical impact. Both vaccines confer similarly high protection against disease caused by vaccine serotypes and lead to a partial replacement by non-vaccine serotypes. PHiD-CV does not protect against serotype 3 disease (not included in the vaccine) and PCV13's effect on this serotype has been inconsistent. PHiD-CV provides some cross-protection against disease caused by vaccine-related serotype 19A but neither vaccine has fully controlled 19A disease. While protection against 19A is higher for PCV13 than PHiD-CV, replacement by non-PCV13 serotypes in settings with a PCV13 program appears to compensate for this difference. This results in a similar residual overall disease burden with both vaccines.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8920200PMC
http://dx.doi.org/10.1080/21645515.2021.1872341DOI Listing

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