Evidence map›Paper›PMID 37889513›Full record

Trial reportThe Journal of infectious diseases2024

RTS,S/AS02A Malaria Vaccine-Induced IgG Responses Equally Recognize Native-Like Fucosylated and Nonfucosylated Plasmodium falciparum Circumsporozoite Proteins.

Chenjerai Jairoce, Dídac Macià, Jorge P Torres-Yaguana, Leonie Mayer, Marta Vidal, Rebeca Santano, Ramón Hurtado-Guerrero, Karine Reiter, David L Narum, Borja Lopez-Gutierrez and 7 more

Registry-linked trialOpen access · bronzeAbstract readRandomized Controlled TrialClinical Trial, Phase II
In one paragraph

Trial report in The Journal of infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00197041 (A Study to Evaluate the Safety, Immunogenicity and Efficacy of GlaxoSmithKline Biologicals' Candidate Malaria Vaccine RTS,S/AS02A, Administered Intramuscularly According to a 0, 1 and 2 Month Vaccination Schedule in Toddlers and Children Aged 1 to 4 Years in a Malaria-endemic Region of Mozambique.), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 84% 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.

NCT00197041 phase2completednot on this map

A Study to Evaluate the Safety, Immunogenicity and Efficacy of GlaxoSmithKline Biologicals' Candidate Malaria Vaccine RTS,S/AS02A, Administered Intramuscularly According to a 0, 1 and 2 Month Vaccination Schedule in Toddlers and Children Aged 1 to 4 Years in a Malaria-endemic Region of Mozambique.

TypeinterventionalSponsorGlaxoSmithKlineRan2003 to 2005Enrolled2,022ConditionsMalariaArmsRTS,S/AS02A
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Trial
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 7 institutions in 5 countries.

Chenjerai JairoceBarcelona Institute for Global Health (ISGlobal), Hospital Clínic-Universitat de Barcelona, Barcelona, Catalonia, Spain.
Dídac MaciàBarcelona Institute for Global Health (ISGlobal), Hospital Clínic-Universitat de Barcelona, Barcelona, Catalonia, Spain.
Jorge P Torres-YaguanaBarcelona Institute for Global Health (ISGlobal), Hospital Clínic-Universitat de Barcelona, Barcelona, Catalonia, Spain.
Leonie MayerBarcelona Institute for Global Health (ISGlobal), Hospital Clínic-Universitat de Barcelona, Barcelona, Catalonia, Spain.
Marta VidalBarcelona Institute for Global Health (ISGlobal), Hospital Clínic-Universitat de Barcelona, Barcelona, Catalonia, Spain.
Rebeca SantanoBarcelona Institute for Global Health (ISGlobal), Hospital Clínic-Universitat de Barcelona, Barcelona, Catalonia, Spain.
Ramón Hurtado-GuerreroInstitute of Biocomputation and Physics of Complex Systems, University of Zaragoza, Zaragoza, Spain.
Karine ReiterLaboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
David L NarumLaboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Borja Lopez-GutierrezEmerging Pathogens Institute, Department of Infectious Diseases and Immunology, College of Veterinary Medicine, University of Florida, Gainesville, Florida, USA.
Timothy HamerlyEmerging Pathogens Institute, Department of Infectious Diseases and Immunology, College of Veterinary Medicine, University of Florida, Gainesville, Florida, USA.
Jahit SacarlalCentro de Investigação em Saúde de Manhiça, Maputo, Mozambique.
Ruth AguilarBarcelona Institute for Global Health (ISGlobal), Hospital Clínic-Universitat de Barcelona, Barcelona, Catalonia, Spain.
Rhoel R DinglasanEmerging Pathogens Institute, Department of Infectious Diseases and Immunology, College of Veterinary Medicine, University of Florida, Gainesville, Florida, USA.
Gemma MoncunillBarcelona Institute for Global Health (ISGlobal), Hospital Clínic-Universitat de Barcelona, Barcelona, Catalonia, Spain.
Luis IzquierdoBarcelona Institute for Global Health (ISGlobal), Hospital Clínic-Universitat de Barcelona, Barcelona, Catalonia, Spain.
Carlota DobañoBarcelona Institute for Global Health (ISGlobal), Hospital Clínic-Universitat de Barcelona, Barcelona, Catalonia, Spain.ORCID 0000-0002-6751-4060
Barcelona Institute for Global Health · ESCentro de Investigación Biomédica en Red · ESUniversity of Florida · USManhiça Health Research Centre · MZNational Institutes of Health · USUniversité Claude Bernard Lyon 1 · FRUniversity of Copenhagen · DK

Funding

EuropeanEuropean CommissionEuropean Social Fund RYC2020-029886-I/AEI/10.13039/501100011033Fondation MérieuxFundación Ramón ArecesGeneralitat de CatalunyaGlaxoSmithKline Biologicals S.AMinistry of Science and Innovation, Spain PID2019-110810RB-I00/AEI/10.13039/501100011033National Institutes of Health, National Institute of Allergy and Infectious DiseasesPATHSocial Fund 2019 FI B 00986Spanish Agency for International Cooperation and DevelopmentSpanish Ministry of Science and Innovation CEX2018-000806-S
6 · The paper itself

Abstract

The RTS,S/AS02A malaria vaccine is based on the Plasmodium falciparum circumsporozoite protein (PfCSP), which is O-fucosylated on the sporozoite surface. We determined whether RTS,S/AS02A-induced immunoglobulin G (IgG) antibodies recognize vaccine-like nonfucosylated PfCSP better than native-like fucosylated PfCSP. Similar to previous vaccine trials, RTS,S/AS02A vaccination induced high anti-PfCSP IgG levels associated with malaria protection. IgG recognition of nonfucosylated and fucosylated PfCSP was equivalent, suggesting that PfCSP fucosylation does not affect antibody recognition. Clinical Trials Registration. NCT00197041.

Indexed as

Malaria, FalciparumMalaria VaccinesAntibodies, ProtozoanHumansImmunoglobulin GPlasmodium falciparumProtozoan ProteinsAntibodies, ProtozoanImmunoglobulin GMalaria VaccinesProtozoan Proteinsantibodiescircumsporozoite protein (PfCSP)fucosylationimmunogenicitymalariaPlasmodium falciparumRTS,S

Identifiers

PMID37889513
PMCPMC11491836
OpenAlexW4387966320

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.