Evidence map›Paper›PMID 39555079›Full record

ArticleFrontiers in immunology2024

ProC6C, a novel multi-stage malaria vaccine, elicits functional antibodies against the minor and central repeats of the Circumsporozoite Protein in human adults.

Jordan Plieskatt, Ebenezer Addo Ofori, Mohammad Naghizadeh, Kazutoyo Miura, Yevel Flores-Garcia, Nis Borbye-Lorenzen, Alfred B Tiono, Kristin Skogstrand, Issaka Sagara, Fidel Zavala and 1 more

Abstract readClinical Trial, Phase I
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Magnitude and durability of ProC6C-AlOH/Matrix-MHuman vaccines & immunotherapeutics · 2025
    Trial
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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

11 authors.

Jordan Plieskatt *Department for Congenital Disorders, Statens Serum Institut (SSI), Copenhagen, Denmark.
Ebenezer Addo Ofori *Department for Congenital Disorders, Statens Serum Institut (SSI), Copenhagen, Denmark.
Mohammad NaghizadehDepartment for Congenital Disorders, Statens Serum Institut (SSI), Copenhagen, Denmark.
Kazutoyo MiuraLaboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, United States.
Yevel Flores-GarciaDepartment of Molecular Microbiology and Immunology, Malaria Research Institute, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.
Nis Borbye-LorenzenDepartment for Congenital Disorders, Statens Serum Institut (SSI), Copenhagen, Denmark.
Alfred B TionoGroupe de Recherche Action en Santé (GRAS), Ouagadougou, Burkina Faso.
Kristin SkogstrandDepartment for Congenital Disorders, Statens Serum Institut (SSI), Copenhagen, Denmark.
Issaka SagaraMalaria Research and Training Center, Mali- National Institute of Allergy and Infectious Diseases International Center for Excellence in Research, University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Fidel ZavalaDepartment of Molecular Microbiology and Immunology, Malaria Research Institute, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.
Michael TheisenDepartment for Congenital Disorders, Statens Serum Institut (SSI), Copenhagen, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: ProC6C is a multi-stage malaria vaccine which includes Methods: The PfCSP response of ProC6C in Burkinabes in the Phase 1 trial (PACTR202201848463189) was profiled through the three vaccine administrations of 100 µg protein on Alhydrogel Results: A single administration of ProC6C-AlOH/Matrix-M seroconverted 19 of 20 volunteers against PfCSP and significantly enhanced antibody titers to major and minor repeats (and present through D180). At D70, ProC6C-AlOH/Matrix-M PfCSP antibodies were found to be similar to responder pools generated from Thai adults receiving RTS,S/AS01. Additionally, ProC6C antibodies were found to be competitive to established PfCSP antibodies such as mAb 317 and mAb L9. The purified and pooled IgG from human volunteers, used in a passive transfer mouse sporozoite challenge model, showed a median of 50% inhibition (P=0.0058). ProC6C PfCSP antibodies were functional in this Discussion: This analysis supports continued investigation of the antibody responses elicited by the ProC6C multi-stage malaria vaccine. This Phase 1 clinical trial demonstrated the short PfCSP sequence included in ProC6C can induce significant PfCSP antibodies in humans, which importantly were determined to be functional.

Indexed as

Antibodies, ProtozoanMalaria, FalciparumMalaria VaccinesPlasmodium falciparumProtozoan ProteinsAdultAnimalsBurkina FasoFemaleHumansMiceSporozoitesYoung AdultAntibodies, Protozoancircumsporozoite protein, ProtozoanMalaria VaccinesProtozoan ProteinsantibodiesCircumsporozoite proteinclinical trialCSPMalariaMatrix-Mvaccine

Identifiers

PMID39555079
PMCPMC11563800

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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.