Evidence map›Paper›PMID 36792575›Full record

ArticleImmunity2023

Potent transmission-blocking monoclonal antibodies from naturally exposed individuals target a conserved epitope on Plasmodium falciparum Pfs230.

Danton Ivanochko, Amanda Fabra-García, Karina Teelen, Marga van de Vegte-Bolmer, Geert-Jan van Gemert, Jocelyn Newton, Anthony Semesi, Marloes de Bruijni, Judith Bolscher, Jordache Ramjith and 15 more

Open access · hybridAbstract read
In one paragraph

Article in Immunity, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
8.4field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Pf8: an open dataset ofWellcome open research · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 9 institutions in 4 countries.

Danton IvanochkoProgram in Molecular Medicine, the Hospital for Sick Children Research Institute, Toronto, ON, Canada.
Amanda Fabra-GarcíaDepartment of Medical Microbiology, Radboudumc, Nijmegen, the Netherlands.
Karina TeelenDepartment of Medical Microbiology, Radboudumc, Nijmegen, the Netherlands.
Marga van de Vegte-BolmerDepartment of Medical Microbiology, Radboudumc, Nijmegen, the Netherlands.
Geert-Jan van GemertDepartment of Medical Microbiology, Radboudumc, Nijmegen, the Netherlands.
Jocelyn NewtonProgram in Molecular Medicine, the Hospital for Sick Children Research Institute, Toronto, ON, Canada.
Anthony SemesiProgram in Molecular Medicine, the Hospital for Sick Children Research Institute, Toronto, ON, Canada.
Marloes de BruijniTropIQ Health Sciences, Nijmegen, the Netherlands.
Judith BolscherTropIQ Health Sciences, Nijmegen, the Netherlands.
Jordache RamjithRadboud Institute for Health Sciences, Department for Health Evidence, Biostatistics Section, Radboudumc, Nijmegen, the Netherlands.
Marta SzabatAbCellera Biologics Inc., Vancouver, BC, Canada.
Stefanie VogtAbCellera Biologics Inc., Vancouver, BC, Canada.
Lucas KraftAbCellera Biologics Inc., Vancouver, BC, Canada.
Sherie DuncanAbCellera Biologics Inc., Vancouver, BC, Canada.
Shwu-Maan LeePATH's Malaria Vaccine Initiative, Washington, DC 20001, USA.
Moses R KamyaInfectious Disease Research Collaboration, Kampala, Uganda.
Margaret E FeeneyDepartment of Medicine, University of California, San Francisco, San Francisco, CA, USA; Department of Pediatrics, University of California, San Francisco, San Francisco, CA, USA.
Prasanna JagannathanDepartment of Microbiology and Immunology, Stanford University, Stanford, CA, USA.
Bryan GreenhouseDepartment of Medicine, University of California, San Francisco, San Francisco, CA, USA.
Robert W SauerweinTropIQ Health Sciences, Nijmegen, the Netherlands.
C Richter KingPATH's Malaria Vaccine Initiative, Washington, DC 20001, USA.
Randall S MacGillPATH's Malaria Vaccine Initiative, Washington, DC 20001, USA.
Teun BousemaDepartment of Medical Microbiology, Radboudumc, Nijmegen, the Netherlands. Electronic address: teun.bousema@radboudumc.nl.
Matthijs M JoreDepartment of Medical Microbiology, Radboudumc, Nijmegen, the Netherlands. Electronic address: matthijs.jore@radboudumc.nl.
Jean-Philippe JulienProgram in Molecular Medicine, the Hospital for Sick Children Research Institute, Toronto, ON, Canada; Departments of Biochemistry and Immunology, University of Toronto, Toronto, ON, Canada. Electronic address: jean-philippe.julien@sickkids.ca.
Radboud University Nijmegen · NLAbCellera (Canada) · CAHospital for Sick Children · CATropIQ Health Sciences · NLU.S. President's Malaria Initiative · USUniversity of California, San Francisco · USInfectious Diseases Research Collaboration · UGStanford University · USUniversity of Toronto · CA

Funding

Transmission ProjectU19AI089674 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MATTHEW G DORSEY, MOSES Robert KAMYA · 2010 to 2026
$29.3M
The role of γδ T cells in fetal and infant immune defense against malariaR01AI093615 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FEENEY, MARGARET E · 2011 to 2025
$9.1M
High-Speed High-Sensitivity Detector for X-ray Micro-Crystallography at GM/CA@APSS10OD012289 · OD · UNIVERSITY OF CHICAGO · PI FISCHETTI, ROBERT F. · 2014 to 2014
$2.0M
Mentoring Translational Researchers for Careers in Pediatric Global HealthK24AI113002 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FEENEY, MARGARET E · 2014 to 2023
$1.9M
Mentoring translational scientists in international infectious disease researchK24AI144048 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Bryan R Greenhouse · 2019 to 2026
$1.6M
NIAID NIH HHS K24 AI113002NIAID NIH HHS K24 AI144048NIAID NIH HHS R01 AI093615NIAID NIH HHS U19 AI089674NIH HHS S10 OD012289
6 · The paper itself

Abstract

Pfs230 is essential for Plasmodium falciparum transmission to mosquitoes and is the protein targeted by the most advanced malaria-transmission-blocking vaccine candidate. Prior understanding of functional epitopes on Pfs230 is based on two monoclonal antibodies (mAbs) with moderate transmission-reducing activity (TRA), elicited from subunit immunization. Here, we screened the B cell repertoire of two naturally exposed individuals possessing serum TRA and identified five potent mAbs from sixteen Pfs230 domain-1-specific mAbs. Structures of three potent and three low-activity antibodies bound to Pfs230 domain 1 revealed four distinct epitopes. Highly potent mAbs from natural infection recognized a common conformational epitope that is highly conserved across P. falciparum field isolates, while antibodies with negligible TRA derived from natural infection or immunization recognized three distinct sites. Our study provides molecular blueprints describing P. falciparum TRA, informed by contrasting potent and non-functional epitopes elicited by natural exposure and vaccination.

Indexed as

Malaria, FalciparumMalaria VaccinesAnimalsAntibodies, MonoclonalAntibodies, ProtozoanAntigens, ProtozoanEpitopesHumansPlasmodium falciparumProtozoan ProteinsAntibodies, MonoclonalAntibodies, ProtozoanAntigens, ProtozoanEpitopesMalaria VaccinesProtozoan Proteinshuman monoclonal antibodiesmalarianatural infectionPfs230Plasmodium falciparumtransmission-blocking

Identifiers

PMID36792575
PMCPMC9942874
OpenAlexW4320730854

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.