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13-valent pneumococcal conjugate vaccine-induced B cells produce serotype 6B but not serotype 3 capsule-specific IgG antibodies in young Malawian adults

  • G. Tembo
  • , D. Hoving
  • , A. C. de Kroon
  • , L. Chimgoneko
  • , T. Nthandira
  • , B. Galafa
  • , F. Thole
  • , E. Nsomba
  • , D. Dula
  • , C. Ngoliwa
  • , N. Toto
  • , L. Makhaza
  • , A. Muyaya
  • , E. Kudowa
  • , A. E. Chirwa
  • , M. Y.R. Henrion
  • , T. Chikaonda
  • , B. C. Urban
  • , D. M. Ferreira
  • , K. C. Jambo
  • S. P. Jochems, S. B. Gordon
  • Malawi-Liverpool-Wellcome Trust Clinical Research Programme
  • Leiden University
  • University of Oxford
  • University of Edinburgh

Research output: Contribution to journalArticlepeer-review

Abstract

Pneumococcal conjugate vaccine (PCV13) introduction has reduced vaccine-type carriage and disease; however pneumococcal carriage persists at high rates particularly in high-transmission settings. Serotype 3 remains a particular problem in Malawi and globally, with high carriage rates, as well as strain resistance to antibiotics and antibody-mediated killing. We studied antibody and B cell responses to PCV13 in 65 healthy Malawian adults (18–40 years) taking part in a randomized controlled trial. Serum, nasal fluid, and PBMC samples were collected before and after vaccination. Anti-capsular IgG for serotypes 3 and 6B were measured by ELISA, and capsule-specific B cells were assessed by spectral flow cytometry. PCV13 increased both serum and mucosal IgG levels, and IgG+ B cells in blood for serotype 6B but not serotype 3. The poor immunogenicity of serotype 3 capsular polysaccharide in Malawian young adults highlights the need for alternative vaccines to address persistent serotype 3 carriage and disease.

Original languageEnglish
Article number128269
JournalVaccine
Volume75
DOIs
Publication statusPublished - 22 Jan 2026

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Anti-CPS
  • PCV13
  • Pneumococcus
  • Polysaccharide-specific B cell

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