Evidence map›Paper›PMID 42562883›Full record

ArticleEMBO molecular medicine2026

Dengue virus envelope epitope-specific antibodies are associated with protection from severe dengue.

Sokchea Lay, Heidi Auerswald, Sievleang Heng, Sopheak Sorn, Sreymom Ken, Veronica Duran, David Esteban Rebellón Sanchez, Daniela Vinueza, Luis Angel Villar Centeno, Fernando Rosso and 8 more

Abstract read
In one paragraph

Article in EMBO molecular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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

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

18 authors.

Sokchea LayImmunology Unit, Institut Pasteur du Cambodge, Pasteur Network, Phnom Penh, Cambodia.
Heidi AuerswaldVirology Unit, Institut Pasteur du Cambodge, Pasteur Network, Phnom Penh, Cambodia. hauerswald@izs.it.ORCID http://orcid.org/0000-0002-4717-7618
Sievleang HengImmunology Unit, Institut Pasteur du Cambodge, Pasteur Network, Phnom Penh, Cambodia.ORCID http://orcid.org/0009-0007-8341-1209
Sopheak SornEpidemiology and Public Health Unit, Institut Pasteur du Cambodge, Pasteur Network, Phnom Penh, Cambodia.
Sreymom KenVirology Unit, Institut Pasteur du Cambodge, Pasteur Network, Phnom Penh, Cambodia.
Veronica DuranDepartment of Medicine, Department of Microbiology and Immunology, Stanford University, Stanford, CA, USA.
David Esteban Rebellón SanchezClinical Research Center, Fundación Valle del Lili, Cali, Colombia.
Daniela VinuezaClinical Research Center, Fundación Valle del Lili, Cali, Colombia.
Luis Angel Villar CentenoCenter for Care and Diagnosis of Infectious Diseases (CDI/INFOVIDA Foundation), Bucaramanga, Colombia.
Fernando RossoClinical Research Center, Fundación Valle del Lili, Cali, Colombia.
Shirit EinavDepartment of Medicine, Department of Microbiology and Immunology, Stanford University, Stanford, CA, USA.
Anavaj SakuntabhaiUnit of Ecology and Emergence of arthropod-borne pathogens, Institut Pasteur, Université Paris Cité, CNRS UMR 2000, 75015, Paris, France.
Felix A ReyStructural Virology Unit, Institut Pasteur, Université Paris Cité, CNRS UMR3569, 75015, Paris, France.ORCID http://orcid.org/0000-0002-9953-7988
Kevin K AriënVirology Unit, Department of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Sowath LyEpidemiology and Public Health Unit, Institut Pasteur du Cambodge, Pasteur Network, Phnom Penh, Cambodia.
Veasna DuongVirology Unit, Institut Pasteur du Cambodge, Pasteur Network, Phnom Penh, Cambodia.
Giovanna Barba-Spaeth *Structural Virology Unit, FlavImmunity Group, Université Paris Cité, Institut Pasteur, Paris, France. giovanna.barba-spaeth@pasteur.fr.
Tineke Cantaert *Immunology Unit, Institut Pasteur du Cambodge, Pasteur Network, Phnom Penh, Cambodia. tineke.cantaert@pasteur.fr.ORCID http://orcid.org/0000-0002-8911-1502

Funding

Inter-regional study of transmission, adaptation and pathogenesis of viruses with pandemic potential in Southeast Asia and West/Central AfricaU01AI151758 · NIAID · INSTITUT PASTEUR · PI SAKUNTABHAI, ANAVAJ, SIMON-LORIERE, ETIENNE · 2020 to 2024
$6.7M
Mechanisms of antibody-dependent enhancement of SARS-CoV-2 infectionR01AI137276 · NIAID · ROCKEFELLER UNIVERSITY · PI Stylianos Bournazos · 2018 to 2026
$4.5M
Advancing the development of a novel class of small molecules for treating pan-coronavirus infectionsR01AI158569 · NIAID · STANFORD UNIVERSITY · PI EINAV, SHIRIT · 2021 to 2025
$3.7M
Comprehensive characterization of the genetic factors and the host immune response associated to protection from clinical Plasmodium vivax malariaR01AI175134 · NIAID · INSTITUT PASTEUR DU CAMBODGE · PI TINEKE CANTAERT, Jean POPOVICI · 2023 to 2026
$2.3M
Defense Threat Reduction Fundamental Research to Counter Weapons of Mass Destruction HDTRA11810039Department of Defense (DoD) office of the Congressionally Directed Medical Research Programs (CDMRP)/Peer Reviewed Medical Research Program (PRMRP), Catalyst and Transformational Awards from Dr. Ralph W81XWH1910235DoD office of the CDMRP/PRMRP W81XWH2210283EC | HORIZON EUROPE Framework Programme (Horizon Europe) 101137033HHS | National Institutes of Health (NIH) 1U01AI151758HHS | National Institutes of Health (NIH) AI137276HHS | National Institutes of Health (NIH) AI175134HHS | National Institutes of Health (NIH) RO1AI158569Institut Pasteur (Pasteur Institute) PTR-212-19NIAID NIH HHS R01 AI137276NIAID NIH HHS R01 AI158569NIAID NIH HHS R01 AI175134NIAID NIH HHS U01 AI151758Wellcome TrustWellcome Trust (WT) 311543/Z/24/Z
6 · The paper itself

Abstract

Our understanding of a protective humoral immune response to dengue virus (DENV) remains limited. The envelope (E) protein is the main antibody (Ab) target. While anti-fusion loop (FL) epitope monoclonal Abs (mAbs) can induce antibody dependent enhancement (ADE) in vitro, some mAbs targeting quaternary epitopes can cross-neutralize different DENV serotypes. However, the contribution of each Ab subset to disease outcome remains poorly characterized. We defined DENV2 E epitope-specific Abs dynamics and assessed their association with disease outcome in a cohort of hospitalized and subclinical dengue patients during post-primary DENV2 infection. We quantified and isolated anti-E epitope-specific Abs and tested their enhancing and neutralizing capacity. During the critical phase, FL-targeting antibodies were increased in hospitalized patients compared to subclinical cases. Antibodies targeting quaternary epitopes were reduced in severe dengue compared to classical dengue fever patients. Functionally, quaternary epitope-targeting antibodies showed stronger neutralization and cross-neutralization properties, while FL-binding antibodies displayed stronger in vitro enhancement. These findings show that anti-DENV2 E epitope-specific Ab proportions correlate with disease susceptibility and severity, with important implications for novel vaccine design.

Indexed as

Antibodies, ViralDengueDengue VirusEpitopesSevere DengueViral Envelope ProteinsAntibodies, MonoclonalAntibodies, NeutralizingFemaleHumansAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralEpitopesViral Envelope Proteins

Identifiers

PMID42562883
PMCPMC13562538

What OpenQuestion holds

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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.