Pfs230 domain 12 is a potent malaria transmission–blocking vaccine candidate

Malaria transmission-blocking vaccines (TBV) target sexual stage parasites that are transmitted to mosquitoes and are critical for spread of the pathogen. The clinically most advanced TBV candidate contains part of the Pro-domain (Pro) and Domain 1 (D1) of <i>Plasmodium falciparum</i> surface protein Pfs230. Subunit vaccines that contain other domains of Pfs230 have so far failed to induce functional antibodies. Here, we produced eight single-domain fragments of Pfs230 in <i>Drosophila melanogaster</i> S2 cells and assessed their immunogenicity in mouse immunizations. In addition to D1-specific antibodies, antibodies raised against D12 showed strong functional transmission-reducing activity in membrane feeding assays with cultured parasites, an activity that was complement dependent. Murine D12-specific antibodies further reduced mosquito transmission of parasites acquired from naturally infected parasite carriers. The D12 antigen was recognized by sera from an all-age cohort of individuals who had been naturally exposed to <i>P. falciparum</i> with antibody levels increasing with age. In conclusion, we identified Pfs230D12 as a promising TBV candidate.

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Publication Details

Journal
Science Advances
Published
2025-11-07
DOI
https://doi.org/10.1126/sciadv.adw8216
Primary Topic
Invertebrate Immune Response Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Pfs230 domain 12 is a potent malaria transmission–blocking vaccine candidate

Eizo Takashima, Dari F. Da, Karina Teelen, Teun Bousema et al.
Science Advances
Invertebrate Immune Response Mechanisms
article

Pfs230 domain 12 is a potent malaria transmission–blocking vaccine candidate

Eizo Takashima, Dari F. Da, Karina Teelen, Teun Bousema, Anna Cohuet, Rianne Stoter, Geert‐Jan van Gemert, Marieke Meijer, Lisanne Hubregtse, Cornelia G. Spruijt, Maartje R. Inklaar, Roch K. Dabiré, Roos M. de Jong, Matthijs M. Jore, Hikaru Nagaoka, Ezra T. Bekkering, Takafumi Tsuboi, Michiel Vermeulen, Emmanuel Arinaitwe, Marga van de Vegte-Bolmer, Sanne Grievink
article en

Abstract

Malaria transmission-blocking vaccines (TBV) target sexual stage parasites that are transmitted to mosquitoes and are critical for spread of the pathogen. The clinically most advanced TBV candidate contains part of the Pro-domain (Pro) and Domain 1 (D1) of <i>Plasmodium falciparum</i> surface protein Pfs230. Subunit vaccines that contain other domains of Pfs230 have so far failed to induce functional antibodies. Here, we produced eight single-domain fragments of Pfs230 in <i>Drosophila melanogaster</i> S2 cells and assessed their immunogenicity in mouse immunizations. In addition to D1-specific antibodies, antibodies raised against D12 showed strong functional transmission-reducing activity in membrane feeding assays with cultured parasites, an activity that was complement dependent. Murine D12-specific antibodies further reduced mosquito transmission of parasites acquired from naturally infected parasite carriers. The D12 antigen was recognized by sera from an all-age cohort of individuals who had been naturally exposed to <i>P. falciparum</i> with antibody levels increasing with age. In conclusion, we identified Pfs230D12 as a promising TBV candidate.

Science AdvancesVol. 11(45)
Centre National de la Recherche Scientifique (FR), Radboud University Nijmegen (NL), Université de Montpellier (FR), Radboud University Medical Center (NL), Maladies Infectieuses et Vecteurs: Écologie, Génétique, Évolution et Contrôle (FR), CellFree Sciences (Japan) (JP), Infectious Diseases Research Collaboration (UG), Institut de Recherche en Sciences de la Santé (BF), Institut de Recherche pour le Développement (FR), Ehime University (JP)
European Commission, Nederlandse Organisatie voor Wetenschappelijk Onderzoek, Radboud Universitair Medisch Centrum, National Institutes of Health
Openalex Percentile: Top 65%
Invertebrate Immune Response Mechanisms
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