Epstein-Barr virus influences the induction of protective antibody responses in young African children vaccinated with the RTS,S malaria vaccine

The RTS,S vaccine provides moderate protection against malaria in children, which may be due in part to environmental factors. Cytomegalovirus (CMV) and Epstein-Barr virus (EBV) infections are prevalent in Africa and potentially contribute to suboptimal vaccine responses. We evaluated whether latent CMV/EBV infections impact RTS,S-induced antibodies in 314 vaccinated children aged 5-29 months in West Africa. While no strong associations were observed for CMV, children seropositive for EBV had lower antigen-specific IgG and IgA, which have been linked with protective malaria immunity. These results may partly explain why malaria vaccines are suboptimal in populations where early CMV/EBV infections are prevalent.

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Publication Details

Journal
medRxiv
Published
2026-11-05
DOI
https://doi.org/10.64898/2026.11.03.26367212
Primary Topic
Malaria Research and Control
Type
preprint
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preprint

Epstein-Barr virus influences the induction of protective antibody responses in young African children vaccinated with the RTS,S malaria vaccine

Jean‐Bosco Ouédraogo, Alassane Dicko, Alexander W. Harris, Halidou Tinto et al.
medRxiv
Malaria Research and Control
preprint

Epstein-Barr virus influences the induction of protective antibody responses in young African children vaccinated with the RTS,S malaria vaccine

Jean‐Bosco Ouédraogo, Alassane Dicko, Alexander W. Harris, Halidou Tinto, Daniel Chandramohan, Brian M Greenwood, Issaka Sagara, Issaka Zongo, Adam Thomas, Liriye Kurtovic, James G. Beeson
preprint en

Abstract

The RTS,S vaccine provides moderate protection against malaria in children, which may be due in part to environmental factors. Cytomegalovirus (CMV) and Epstein-Barr virus (EBV) infections are prevalent in Africa and potentially contribute to suboptimal vaccine responses. We evaluated whether latent CMV/EBV infections impact RTS,S-induced antibodies in 314 vaccinated children aged 5-29 months in West Africa. While no strong associations were observed for CMV, children seropositive for EBV had lower antigen-specific IgG and IgA, which have been linked with protective malaria immunity. These results may partly explain why malaria vaccines are suboptimal in populations where early CMV/EBV infections are prevalent.

medRxiv
Burnet Institute (AU), London School of Hygiene & Tropical Medicine (GB), Université des Sciences, des Techniques et des Technologies de Bamako (ML), Institut de Recherche en Sciences de la Santé (BF)
Malaria Research and Control
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