Evidence map›Paper›PMID 40980580›Full record

ArticleOpen forum infectious diseases2025

Anti-Nonstructural Protein 1 Antibody Kinetics and Their Association With Disease Severity in Pediatric Dengue.

Sansanee Noisakran, Patchanika Hengtrakool, Kattaleeya Jindapornprasert, Chunya Puttikhunt, Tanapan Prommool, Nattaya Tangthawornchaikul, Nuttapong Kaewjiw, Pucharee Songprakhon, Kanokwan Sriruksa, Wannee Limpitikul and 3 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the 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
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

1 citing paper in PubMed.

  1. 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

13 authors.

Sansanee NoisakranMolecular Biology of Dengue and Flaviviruses Research Team, Medical Molecular Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Bangkok, Thailand.ORCID https://orcid.org/0000-0002-9336-3331
Patchanika HengtrakoolDepartment of Immunology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Kattaleeya JindapornprasertMolecular Biology of Dengue and Flaviviruses Research Team, Medical Molecular Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Bangkok, Thailand.
Chunya PuttikhuntMolecular Biology of Dengue and Flaviviruses Research Team, Medical Molecular Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Bangkok, Thailand.ORCID https://orcid.org/0000-0003-1611-2667
Tanapan PrommoolMolecular Biology of Dengue and Flaviviruses Research Team, Medical Molecular Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Bangkok, Thailand.ORCID https://orcid.org/0000-0002-1967-2670
Nattaya TangthawornchaikulMolecular Biology of Dengue and Flaviviruses Research Team, Medical Molecular Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Bangkok, Thailand.ORCID https://orcid.org/0009-0005-2055-8217
Nuttapong KaewjiwDivision of Dengue Hemorrhagic Fever Research, Department of Research, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Pucharee SongprakhonDivision of Molecular Medicine, Department of Research, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Kanokwan SriruksaDepartment of Pediatric, Khon Kaen Hospital, Ministry of Public Health, Khon Kaen, Thailand.
Wannee LimpitikulDepartment of Pediatric, Songkhla Hospital, Ministry of Public Health, Songkhla, Thailand.
Dumrong MairiangMolecular Biology of Dengue and Flaviviruses Research Team, Medical Molecular Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Bangkok, Thailand.ORCID https://orcid.org/0000-0002-2743-0145
Panisadee AvirutnanDivision of Dengue Hemorrhagic Fever Research, Department of Research, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.ORCID https://orcid.org/0000-0003-0053-3045
Prida MalasitMolecular Biology of Dengue and Flaviviruses Research Team, Medical Molecular Biotechnology Research Group, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Bangkok, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Dengue is an immune-mediated disease with severe manifestations often linked to secondary infections. Dengue virus nonstructural protein 1 (DENV NS1) and corresponding antibodies are thought to play a crucial role in disease pathogenesis. Methods: This study investigated the kinetics of anti-NS1 antibody responses in relation to NS1 levels and NS1 immune complexes (ICs) in pediatric dengue patients with varying disease severity following secondary DENV infections with all four serotypes, using retrospective plasma samples collected in Thailand and analyzed by enzyme-linked immunosorbent assays (ELISAs). Plasma samples from pediatric patients with other febrile illnesses (OFI) and healthy adults served as non-dengue control groups. Results: Anti-NS1 IgG (particularly IgG1 and IgG4) and IgA persisted for at least 6 months after illness and were associated with increased dengue severity, whereas the shorter-lived anti-NS1 IgM was higher in patients with milder dengue. Anti-NS1 IgG also persisted notably longer than anti-DENV IgG. Anti-NS1 IgG3 showed a transient surge across all four serotypes, suggesting its potential as a marker of recent infection. NS1 proteins and NS1 ICs were positively correlated, inversely related to anti-NS1 IgG, and strongly associated with severe dengue. Conclusions: Anti-NS1 antibody isotypes and IgG subclasses exhibited distinct associations with dengue severity, influenced by both infecting serotypes and time since illness onset. Correlations among NS1, anti-NS1 antibodies, and NS1 ICs were observed during the acute phase of secondary infection, potentially influencing dengue disease outcomes. These findings enhance our understanding of dengue immunopathogenesis and may inform improved diagnostic and surveillance tools.

Indexed as

antibody isotypes and IgG subclassesanti-NS1 antibodydengueimmune complexesNS1 protein

Identifiers

PMID40980580
PMCPMC12448948

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.