Persistence of Anti-SE36 Antibodies Induced by the Malaria Vaccine Candidate BK-SE36/CpG in 5–10-Year-Old Burkinabe Children Naturally Exposed to Malaria

Author:

Nebie Issa1,Palacpac Nirianne Marie Q.2ORCID,Bougouma Edith Christiane1,Diarra Amidou1,Ouédraogo Alphonse1ORCID,D’Alessio Flavia3,Houard Sophie3,Tiono Alfred B.1ORCID,Cousens Simon4,Horii Toshihiro2,Sirima Sodiomon B.1ORCID

Affiliation:

1. Groupe de Recherche Action en Santé (GRAS), Ouagadougou 10248, Burkina Faso

2. Department of Malaria Vaccine Development, Research Institute for Microbial Diseases, Osaka University, Suita 565-0871, Osaka, Japan

3. European Vaccine Initiative, UniversitätsKlinikum Heidelberg, Voßstraße 2, 69115 Heidelberg, Germany

4. Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, London WC1E 7HT, UK

Abstract

Information on the dynamics and decline/persistence of antibody titres is important in vaccine development. A recent vaccine trial in malaria-exposed, healthy African adults and children living in a malaria hyperendemic and seasonal area (Ouagadougou, Burkina Faso) was the first study in which BK-SE36/CpG was administered to different age groups. In 5- to 10-year-old children, the risk of malaria infection was markedly lower in the BK-SE36/CpG arm compared to the control arm. We report here data on antibody titres measured in this age-group after the high malaria transmission season of 2021 (three years after the first vaccine dose was administered). At Year 3, 83% of children had detectable anti-SE36 total IgG antibodies. Geometric mean antibody titres and the proportion of children with detectable anti-SE36 antibodies were markedly higher in the BK-SE36/CpG arm than the control (rabies) arm. The information obtained in this study will guide investigators on future vaccine/booster schedules for this promising blood-stage malaria vaccine candidate.

Funder

Global Health Innovative Technology Fund

Translational Research Network Program

NPC

Publisher

MDPI AG

Reference56 articles.

1. World Health Organization (2024, January 18). World Malaria Report, Available online: https://www.who.int/teams/global-malaria-programme/reports/world-malaria-report-2023.

2. Correlating efficacy and immunogenicity in malaria vaccine trials;McCall;Semin. Immunol.,2018

3. Malaria Vaccines: Progress to Date;Stanisic;BioDrugs,2023

4. Takashima, E., Otsuki, H., Morita, M., Ito, D., Nagaoka, H., Yuguchi, T., Hassan, I., and Tsuboi, T. (2024). The need for novel asexual blood-stage malaria vaccine candidates for Plasmodium falciparum. Biomolecules, 14.

5. World Health Organization (2024, January 18). Global Technical Strategy for Malaria 2016–2030, 2021 Update. Available online: https://www.who.int/publications/i/item/9789240031357.

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