Published December 8, 2018
| Version v1
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Data from: Unravelling the immune signature of Plasmodium falciparum transmission-reducing immunity
Authors/Creators
- Stone, Will J. R.1
- Campo, Joseph J.2
- Ouédraogo, André Lin3
- Meerstein-Kessel, Lisette1
- Morlais, Isabelle4
- Da, Dari5
- Cohuet, Anna6
- Nsango, Sandrine4
- Sutherland, Colin J.7
- van de Vegte-Bolmer, Marga8
- Siebelink-Stoter, Rianne8
- van Gemert, Geert-Jan8
- Graumans, Wouter8
- Lanke, Kjerstin8
- Shandling, Adam D.2
- Pablo, Jozelyn V.2
- Teng, Andy A.2
- Jones, Sophie7
- de Jong, Roos M.8
- Fabra-García, Amanda8
- Bradley, John9
- Roeffen, Will8
- Lasonder, Edwin10
- Gremo, Giuliana11
- Schwarzer, Evelin11
- Drakeley, Chris J.7
- Singh, Susheel K.12
- Theisen, Michael12
- Felgner, Phil13
- Marti, Matthias14
- Sauerwein, Robert1
- Bousema, Teun1
- Jore, Matthijs M.8
- 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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Additional details
Related works
- Is cited by
- 10.1038/s41467-017-02646-2 (DOI)