Evidence map›Paper›PMID 42236711›Full record

ArticleNature communications2026

Heterogeneity and dynamics of DENV-specific CD8 + T cells in dengue infection.

Sirawit Srikor, Waradon Sungnak, Chawinya Trakoolsoontorn, Tiraput Poonpanichakul, Natnicha Jiravejchakul, Damita Jevapatarakul, Narita Thungsatianpun, Anunya Opasawatchai, Lisa Dratva, Lorenz Kretschmer and 11 more

Abstract read
In one paragraph

Article in Nature communications, 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

21 authors.

Sirawit Srikor *Department of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.ORCID http://orcid.org/0009-0008-1528-3441
Waradon Sungnak *Department of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.ORCID http://orcid.org/0000-0002-0136-4960
Chawinya TrakoolsoontornDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Tiraput PoonpanichakulDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.ORCID http://orcid.org/0000-0002-3651-3575
Natnicha JiravejchakulDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Damita JevapatarakulDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.ORCID http://orcid.org/0000-0002-8126-6964
Narita ThungsatianpunDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Anunya OpasawatchaiIntegrative Computational BioScience (ICBS) Center, Mahidol University, Nakhon Pathom, Thailand.
Lisa DratvaCambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, Cambridge Biomedical Campus, University of Cambridge, Cambridge, UK.
Lorenz KretschmerCambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, Cambridge Biomedical Campus, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0003-0987-8429
DENFREE Thailand
Oranart MatangkasombutDepartment of Microbiology and Center of Excellence on Oral Microbiology and Immunology, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.
Gavin ScreatonCAMS Oxford Institute, Chinese Academy of Medical Sciences & Peking Union Medical College, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-3549-4309
Wanwisa DejnirattisaiDivision of Emerging Infectious Disease, Research Department, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkoknoi, Bangkok, Thailand.
Thaneeya DuangchindaMolecular Biology of Dengue and Flaviviruses Research Team, National Center for Genetic Engineering and Biotechnology, National Science and Development Agency, NSTDA, Pathum Thani, Thailand.
Jongeun ParkGraduate School of Medical Science and Engineering, KAIST, Daejeon, Republic of Korea.ORCID http://orcid.org/0000-0002-1687-2423
Kerstin MeyerWellcome Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, UK.
Juthathip MongkolsapayaCAMS Oxford Institute, Chinese Academy of Medical Sciences & Peking Union Medical College, University of Oxford, Oxford, UK.
Varodom CharoensawanIntegrative Computational BioScience (ICBS) Center, Mahidol University, Nakhon Pathom, Thailand. varodom.cha@mahidol.ac.th.ORCID http://orcid.org/0000-0002-2199-4126
Sarah A TeichmannCambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, Cambridge Biomedical Campus, University of Cambridge, Cambridge, UK. sat1003@cam.ac.uk.ORCID http://orcid.org/0000-0002-6294-6366
Ponpan MatangkasombutDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand. ponpan.mat@mahidol.ac.th.ORCID http://orcid.org/0000-0003-0101-4386

Funding

National Science and Technology Development Agency (NSTDA) FDA-CO-561-7176-THWellcome Trust
6 · The paper itself

Abstract

Dengue virus (DENV) is a major global health threat, with secondary heterotypic infections potentially inducing detrimental memory immune responses. Antigen-specific CD8 + T cells contribute to both protection and pathogenicity, yet how their phenotypic heterogeneity relates to disease severity remains unclear. Here, we performed plate-based single-cell RNA sequencing of circulating DENV-specific CD8 + T cells identified by HLA tetramers loaded with DENV NS3-derived epitopes. Using tetramer binding to peptides corresponding to the currently and serologically inferred dominant previously infecting serotypes, we identify distinct CD8 + T cell subsets associated with disease severity. Asymptomatic dengue is enriched for lower tetramer binding cells with moderate cytotoxic programs, whereas dengue hemorrhagic fever is associated with high tetramer binding CX3CR1 + CD8 + T cells exhibiting enhanced expression of genes related to T cell receptor signaling and cytotoxicity. T cell receptor repertoires are similar among symptomatic cases but displayed temporal dynamics. Overall, DENV NS3-specific CD8 + T cells across disease severity and time are associated with distinct transcriptomic states and T cell receptor features.

Indexed as

CD8-Positive T-LymphocytesDengueDengue VirusCX3C Chemokine Receptor 1DEAD-box RNA HelicasesEpitopes, T-LymphocyteHumansNucleoside-TriphosphataseReceptors, Antigen, T-CellSerine EndopeptidasesSevere DengueSingle-Cell AnalysisViral Nonstructural ProteinsViral ProteasesCX3C Chemokine Receptor 1CX3CR1 protein, humanDEAD-box RNA HelicasesEpitopes, T-LymphocyteNS3 protein, flavivirusNucleoside-TriphosphataseReceptors, Antigen, T-CellSerine EndopeptidasesViral Nonstructural ProteinsViral Proteases

Identifiers

PMID42236711
PMCPMC13392236

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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.