Published December 8, 2018 | Version v1
Dataset Open

Data from: Unravelling the immune signature of Plasmodium falciparum transmission-reducing immunity

  • 1. Radboud University Nijmegen
  • 2. Antigen Discovery Inc., Irvine, USA*
  • 3. Bellevue Hospital Center
  • 4. Organisation de Coordination pour la lutte contre les Endémies en Afrique Centrale
  • 5. Nazi Boni University
  • 6. French National Centre for Scientific Research
  • 7. London School of Hygiene & Tropical Medicine
  • 8. Radboud Institute for Molecular Life Sciences
  • 9. Medical Research Council
  • 10. Plymouth University
  • 11. University of Turin
  • 12. Statens Serum Institut
  • 13. University of California, Irvine
  • 14. Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, USA*

Description

Infection with Plasmodium can elicit antibodies that inhibit parasite survival in the mosquito, when they are ingested in an infectious blood meal. Here, we determine the transmission-reducing activity (TRA) of naturally acquired antibodies from 648 malaria-exposed individuals using lab-based mosquito-feeding assays. Transmission inhibition is significantly associated with antibody responses to Pfs48/45, Pfs230, and to 43 novel gametocyte proteins assessed by protein microarray. In field-based mosquito-feeding assays the likelihood and rate of mosquito infection are significantly lower for individuals reactive to Pfs48/45, Pfs230 or to combinations of the novel TRA-associated proteins. We also show that naturally acquired purified antibodies against key transmission-blocking epitopes of Pfs48/45 and Pfs230 are mechanistically involved in TRA, whereas sera depleted of these antibodies retain high-level, complement-independent TRA. Our analysis demonstrates that host antibody responses to gametocyte proteins are associated with reduced malaria transmission efficiency from humans to mosquitoes.

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