Evidence map›Paper›PMID 36792574›Full record

ArticleImmunity2023

Highly potent, naturally acquired human monoclonal antibodies against Pfs48/45 block Plasmodium falciparum transmission to mosquitoes.

Amanda Fabra-García, Sophia Hailemariam, Roos M de Jong, Kirsten Janssen, Karina Teelen, Marga van de Vegte-Bolmer, Geert-Jan van Gemert, Danton Ivanochko, Anthony Semesi, Brandon McLeod and 18 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 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
11.3field-weighted citation impact, top 1% 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

22 citing papers in PubMed, 37 citations in OpenAlex.

  1. Magnitude and durability of ProC6C-AlOH/Matrix-MHuman vaccines & immunotherapeutics · 2025
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  14. Seroprevalence of antibodies toFrontiers in immunology · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors at 9 institutions in 4 countries.

Amanda Fabra-GarcíaDepartment of Medical Microbiology, Radboudumc, Nijmegen, the Netherlands.
Sophia HailemariamProgram in Molecular Medicine, The Hospital for Sick Children Research Institute, Toronto, ON, Canada; Department of Biochemistry, University of Toronto, Toronto, ON, Canada.
Roos M de JongDepartment of Medical Microbiology, Radboudumc, Nijmegen, the Netherlands.
Kirsten JanssenDepartment 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.
Danton IvanochkoProgram 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.
Brandon McLeodProgram in Molecular Medicine, The Hospital for Sick Children Research Institute, Toronto, ON, Canada; Department of Biochemistry, University of Toronto, Toronto, ON, Canada.
Martijn W VosTropIQ Health Sciences, Nijmegen, the Netherlands.
Marloes H C de BruijniTropIQ Health Sciences, Nijmegen, the Netherlands.
Judith M BolscherTropIQ Health Sciences, 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.
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.
Koen J DecheringTropIQ Health Sciences, Nijmegen, the Netherlands.
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.
Jean-Philippe JulienProgram in Molecular Medicine, The Hospital for Sick Children Research Institute, Toronto, ON, Canada; Department of Biochemistry, University of Toronto, Toronto, ON, Canada; Department of Immunology, University of Toronto, Toronto, ON, Canada. Electronic address: jean-philippe.julien@sickkids.ca.
Matthijs M JoreDepartment of Medical Microbiology, Radboudumc, Nijmegen, the Netherlands. Electronic address: matthijs.jore@radboudumc.nl.
Radboud University Nijmegen · NLTropIQ Health Sciences · NLAbCellera (Canada) · CAUniversity of Toronto · CAHospital for Sick Children · CAUniversity of California, San Francisco · USU.S. President's Malaria Initiative · USInfectious Diseases Research Collaboration · UGStanford University · US

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

Malaria transmission-blocking vaccines (TBVs) aim to induce antibodies that interrupt malaria parasite development in the mosquito, thereby blocking onward transmission, and provide a much-needed tool for malaria control and elimination. The parasite surface protein Pfs48/45 is a leading TBV candidate. Here, we isolated and characterized a panel of 81 human Pfs48/45-specific monoclonal antibodies (mAbs) from donors naturally exposed to Plasmodium parasites. Genetically diverse mAbs against each of the three domains (D1-D3) of Pfs48/45 were identified. The most potent mAbs targeted D1 and D3 and achieved >80% transmission-reducing activity in standard membrane-feeding assays, at 10 and 2 μg/mL, respectively. Co-crystal structures of D3 in complex with four different mAbs delineated two conserved protective epitopes. Altogether, these Pfs48/45-specific human mAbs provide important insight into protective and non-protective epitopes that can further our understanding of transmission and inform the design of refined malaria transmission-blocking vaccine candidates.

Indexed as

CulicidaeMalariaMalaria, FalciparumMalaria VaccinesAnimalsAntibodies, MonoclonalAntibodies, ProtozoanHumansPlasmodium falciparumProtozoan ProteinsAntibodies, MonoclonalAntibodies, ProtozoanMalaria VaccinesProtozoan Proteinscrystallographyhuman monoclonal antibodiesmalariaPfs48/45Plasmodium falciparumtransmission-blocking vaccinetransmission-reducing activity

Identifiers

PMID36792574
PMCPMC9942873
OpenAlexW4320730822

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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 OpenQuestion graph.