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February 28, 2026npj Vaccines0 citationsOpen Access

Pooled analysis of PCV13 efficacy from controlled human infection trials in Malawi and the UK

EKEvaristar KudowaGTGodwin TemboACAnthony E. Chirwa

Key Points

  • This analysis aims to evaluate the efficacy of the PCV13 vaccine against pneumococcal serotype 6B carriage and explore sex-based differences.
  • Conducted pooled analysis of two randomised controlled trials in Malawi and the UK.
  • Examined vaccine efficacy and immunological responses based on sex differences.
  • Measured colonisation rates and IgG titres pre- and post-vaccination.
  • PCV-13 reduced pneumococcal colonisation by 76% (p < 0.001).
  • Female carriers exhibited higher carriage rates (28% vs. 19%, p = 0.066).
  • Baseline IgG titres were significantly higher in females in Malawi (2.62 µg/ml vs. 2.05 µg/ml, p = 0.015).
  • Post-vaccination IgG titres did not differ by sex.

Abstract

Abstract We conducted the first pooled analysis of two randomised controlled vaccine trials on experimental pneumococcal serotype 6B carriage, registered in Malawi (PACTR202008503507113) and the UK (ISRCTN45340436). This post-hoc exploratory study examined the sex-based differences in carriage, vaccine efficacy and vaccine-induced responses. PCV-13 reduced colonisation by 76% ( p < 0.001) with non-significant interaction by sex (RR = 1.549, p = 0.413). Females showed a higher carriage rate than males (28% vs. 19%, p = 0.066). Baseline anti-6B Capsular Polysaccharide Immunoglobulin G (IgG) titres were higher in females, significantly in Malawi (2.62 µg/ml vs males 2.05 µg/ml, p = 0.015). Post-vaccination titres did not differ by sex. The pooled fold change in IgG pre-post vaccination, was higher in vaccinated females (5.47 vs 3.30, p = 0.053). This analysis demonstrates the utility and challenges of integrating CHIM data between diverse settings to evaluate vaccine efficacy, describe inter-setting differences, investigate biological and immunological factors influencing protection against pneumococcal carriage and ultimately inform future vaccine development strategies.

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Cite This Study

Kudowa et al. (2026) studied this question.

synapsesocial.com/papers/69a2877b0a974eb0d3c033a5https://doi.org/10.1038/s41541-026-01381-4
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