Evidence map›Paper›PMID 29078270›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Synergistic malaria vaccine combinations identified by systematic antigen screening.

Leyla Y Bustamante, Gareth T Powell, Yen-Chun Lin, Michael D Macklin, Nadia Cross, Alison Kemp, Paula Cawkill, Theo Sanderson, Cecile Crosnier, Nicole Muller-Sienerth and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
7.4field-weighted citation impact, top 3% 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

42 citing papers in PubMed, 64 citations in OpenAlex.

  1. Trial
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  3. An mRNA-lipid nanoparticle vaccine targeting theMolecular therapy. Nucleic acids · 2026
    Article
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  7. Cells · 2025
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  20. Biophysical Tools and Concepts Enable Understanding of Asexual Blood Stage Malaria.Frontiers in cellular and infection microbiology · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 2 countries.

Leyla Y BustamanteMalaria Programme, Wellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom.
Gareth T PowellCell Surface Signalling Laboratory, Wellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom.
Yen-Chun LinCavendish Laboratory, University of Cambridge, Cambridge CB3 0HE, United Kingdom.
Michael D MacklinDivision of Infectious Diseases, Department of Medicine, Indiana University School of Medicine, Indianapolis, IN 46202.
Nadia CrossMalaria Programme, Wellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom.
Alison KempMalaria Programme, Wellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom.
Paula CawkillMalaria Programme, Wellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom.
Theo SandersonMalaria Programme, Wellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom.
Cecile CrosnierCell Surface Signalling Laboratory, Wellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom.
Nicole Muller-SienerthCell Surface Signalling Laboratory, Wellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom.
Ogobara K DoumboMalaria Research and Training Centre, Department of Epidemiology of Parasitic Diseases, International Center of Excellence in Research, University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Boubacar TraoreMalaria Research and Training Centre, Department of Epidemiology of Parasitic Diseases, International Center of Excellence in Research, University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Peter D CromptonLaboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852.
Pietro CicutaCavendish Laboratory, University of Cambridge, Cambridge CB3 0HE, United Kingdom.ORCID 0000-0002-9193-8496
Tuan M TranDivision of Infectious Diseases, Department of Medicine, Indiana University School of Medicine, Indianapolis, IN 46202.ORCID 0000-0002-1928-861X
Gavin J WrightCell Surface Signalling Laboratory, Wellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom.
Julian C RaynerMalaria Programme, Wellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom; julian.rayner@sanger.ac.uk.
Wellcome Sanger Institute · GBIndiana University School of MedicineUniversity of Cambridge · GBNational Institutes of Health · US

Funding

Mechanisms of naturally-acquired immunity to malaria and clinical trials of anti-malaria monoclonal antibodiesZIAAI001155 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI CROMPTON, PETER · 2011 to 2025
$30.9M
Defining clinical and sterile immunity to Plasmodium falciparum infection using systems biology approachesK08AI125682 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI TRAN, TUAN MANH · 2017 to 2021
$926k
Indiana Clinical and Translational Science Institute-K12 ProgramKL2TR000163 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI SHEKHAR, ANANTHA · 2012 to 2013
$720k
Medical Research Council MR/J002283/1NCATS NIH HHS KL2 TR000163NIAID NIH HHS K08 AI125682Wellcome TrustWellcome Trust 090851
6 · The paper itself

Abstract

A highly effective vaccine would be a valuable weapon in the drive toward malaria elimination. No such vaccine currently exists, and only a handful of the hundreds of potential candidates in the parasite genome have been evaluated. In this study, we systematically evaluated 29 antigens likely to be involved in erythrocyte invasion, an essential developmental stage during which the malaria parasite is vulnerable to antibody-mediated inhibition. Testing antigens alone and in combination identified several strain-transcending targets that had synergistic combinatorial effects in vitro, while studies in an endemic population revealed that combinations of the same antigens were associated with protection from febrile malaria. Video microscopy established that the most effective combinations targeted multiple discrete stages of invasion, suggesting a mechanistic explanation for synergy. Overall, this study both identifies specific antigen combinations for high-priority clinical testing and establishes a generalizable approach that is more likely to produce effective vaccines.

Indexed as

Antibodies, ProtozoanAntigens, ProtozoanCell LineErythrocytesHEK293 CellsHumansMalaria, FalciparumMalaria VaccinesPlasmodium falciparumProspective StudiesProtozoan ProteinsAntibodies, ProtozoanAntigens, ProtozoanMalaria VaccinesProtozoan Proteinsantigen combinationserythrocyte invasionmalariaPlasmodium falciparumvaccine

Identifiers

PMID29078270
PMCPMC5692528
OpenAlexW2765989691

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.