Evidence map›Paper›PMID 42030969›Full record

Trial reportThe Lancet. Infectious diseases2026

Duration and association with protection of NANP-repeat-specific and C-terminus-specific anti-circumsporozoite protein IgG responses following RTS,S/AS01

Maria Lara-Escandell, Lina Sánchez, Dídac Macià, Chenjerai Jairoce, Maxmillian Mpina, Hermann Sorgho, Selidji Todagbe Agnandji, David Dosoo, Ben Gyan, Marta Vidal and 17 more

Erratum issuedAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The Lancet. Infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors.

Maria Lara-EscandellISGlobal, Barcelona, Spain; Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, Barcelona, Spain.
Lina SánchezISGlobal, Barcelona, Spain; Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, Barcelona, Spain.
Dídac MaciàISGlobal, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), Barcelona, Spain.
Chenjerai JairoceManhiça Health Research Center (CISM), Maputo, Mozambique.
Maxmillian MpinaBiomedical Research and Clinical Trials Department, Ifakara Health Institute, Tanzania.
Hermann SorghoUnité de Recherche Clinique de Nanoro, Institut de Recherche en Sciences de la Santé, Nanoro, Burkina Faso.
Selidji Todagbe AgnandjiCentre de Recherches Médicales de Lambaréné (CERMEL), Lambaréné, Gabon; Institute of Medical Microbiology, University Hospital Münster, Münster, Germany.
David DosooKintampo Health Research Centre, Research & Development Division, Ghana Health Service, Kintampo, Ghana.
Ben GyanKintampo Health Research Centre, Research & Development Division, Ghana Health Service, Kintampo, Ghana; Noguchi Memorial Institute for Medical Research, University of Ghana, Accra, Ghana.
Marta VidalISGlobal, Barcelona, Spain.
Alfons JiménezISGlobal, Barcelona, Spain; Centro de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), Barcelona, Spain.
Robert Andrew MitchellISGlobal, Barcelona, Spain; Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, Barcelona, Spain.
Daniel Medina-ExpósitoISGlobal, Barcelona, Spain.
Laura PuyolISGlobal, Barcelona, Spain.
Rebeca SantanoISGlobal, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), Barcelona, Spain.
Sheetij DuttaWalter Reed Army Institute of Research, Silver Spring, MD, USA.
Seth Owusu-AgyeiKintampo Health Research Centre, Research & Development Division, Ghana Health Service, Kintampo, Ghana.
Kwaku Poku AsanteKintampo Health Research Centre, Research & Development Division, Ghana Health Service, Kintampo, Ghana.
Halidou TintoUnité de Recherche Clinique de Nanoro, Institut de Recherche en Sciences de la Santé, Nanoro, Burkina Faso.
Pedro AideManhiça Health Research Center (CISM), Maputo, Mozambique.
Augusto NhabombaManhiça Health Research Center (CISM), Maputo, Mozambique.
Benjamin MordmüellerCentro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), Barcelona, Spain; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, Netherlands.
Claudia DaubenbergerUniversity of Basel, Basel, Switzerland; Swiss Tropical and Public Health Institute, Allschwil, Switzerland.
Ruth AguilarISGlobal, Barcelona, Spain.
John WaitumbiUS Army Medical Research Directorate-Africa, Kenya Medical Research Institute, Nairobi, Kenya.
Gemma MoncunillISGlobal, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), Barcelona, Spain. Electronic address: gemma.moncunill@isglobal.org.
Carlota DobañoISGlobal, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), Barcelona, Spain. Electronic address: carlota.dobano@isglobal.org.

Funding

Baseline host and environmental factors that impact pre-erythrocytic malaria vaccine (hypo)responsiveness in endemic regionsU01AI165745 · NIAID · LEIDEN UNIVERSITY MEDICAL CENTER · PI Maria Yazdanbakhsh · 2022 to 2026
$3.3M
Understanding RTS,S malaria vaccine-induced protection through integrated analysiR01AI095789 · NIAID · BARCELONA INTERNATIONAL HEALTH RES CTR · PI DOBANO, CARLOTA · 2012 to 2016
$3.2M
NIAID NIH HHS R01 AI095789NIAID NIH HHS U01 AI165745
6 · The paper itself

Abstract

backgroundThe RTS,S/AS01

methodsIn this observational study, we evaluated IgG responses to NANP-repeat, C-terminus, and full-length circumsporozoite protein constructs at five timepoints before and after primary and booster vaccination, in children aged 5-17 months from six African countries enrolled in the RTS,S/AS01

findingsBetween May 25, 2009, to March 5, 2010, 1292 children were recruited and included for analysis in this study. IgG levels declined more slowly for C-terminus than for NANP-repeat over 17 months after primary vaccination (geometric mean fold change 0·099 [95% CI 0·089-0·110] vs 0·055 [0·048-0·062]; p<0·0001). The booster significantly enhanced C-terminal IgG, exceeding post-primary peak levels (geometric mean fold change 1·98 [95% CI 1·77-2·21]), whereas NANP-repeat responses were restored but remained below post-primary levels (geometric mean fold changes 0·57 [95% CI 0·51-0·63]). Higher circumsporozoite protein IgG levels correlated with reduced malaria risk, particularly during maintenance phases, with stronger associations for C-terminus, which remained independently protective after adjustment for NANP-repeat antibodies (hazard ratio 0·60, 95% CI 0·43-0·83; p=0·0021). After boosting, maintenance but not peak IgG levels correlated with reduced malaria risk.

interpretationIgG to circumsporozoite protein C-terminus are more durable than those to the NANP-repeats. Antibody maintenance emerges as a stronger predictor of RTS,S/AS01

fundingUSA National Institute of Allergy and Infectious Diseases, National Institutes of Health; PATH and Malaria Vaccine Initiative; Spanish Ministerio de Economía y Competitividad; Instituto de Salud Carlos III; CERCA programme; and Secretaria d'Universitats i Recerca del Departament d'Empresa i Coneixement, Generalitat de Catalunya.

Indexed as

Antibodies, ProtozoanImmunoglobulin GMalaria, FalciparumMalaria VaccinesPlasmodium falciparumProtozoan ProteinsFemaleHumansInfantMaleVaccinationAntibodies, Protozoancircumsporozoite protein, ProtozoanImmunoglobulin GMalaria VaccinesProtozoan ProteinsRTS,S-AS01E vaccine

Identifiers

PMID42030969
PMCPMC13261563

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.