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
Authors:
- Issa NebieIssa Nebie
- Nirianne Marie Q. PalacpacNirianne Marie Q. Palacpac
- Edith Christiane BougoumaEdith Christiane Bougouma
- Amidou DiarraAmidou Diarra
- Alphonse OuédraogoAlphonse Ouédraogo
- Flavia D’alessioFlavia D’alessio
- Sophie HouardSophie Houard
- Alfred B. TionoAlfred B. Tiono
- Simon CousensSimon Cousens
- Toshihiro HoriiToshihiro Horii
- Sodiomon B. SirimaSodiomon B. Sirima
Open Access
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.Keywords
Funding Information
- Global Health Innovative Technology Fund (G2016-106, G2019-208, JP20lm0203135, AMED)
- Translational Research Network program (G2016-106, G2019-208, JP20lm0203135, AMED)
- NPC (G2016-106, G2019-208, JP20lm0203135, AMED)
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