Evidence map›Paper›PMID 37055751›Full record

ArticleJournal of biomedical science2023

Integrated systems immunology approach identifies impaired effector T cell memory responses as a feature of progression to severe dengue fever.

Lisa J Ioannidis, Stephanie I Studniberg, Emily M Eriksson, Suhendro Suwarto, Dionisius Denis, Yang Liao, Wei Shi, Alexandra L Garnham, R Tedjo Sasmono, Diana S Hansen

Open access · diamondAbstract read
In one paragraph

Article in Journal of biomedical science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 19% 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.

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

9 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. T Cell Responses During Dengue Infection.Current topics in microbiology and immunology · 2026
    Review
  7. Review
  8. Review
  9. Article
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

10 authors at 4 institutions in 3 countries.

Lisa J Ioannidis *The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Stephanie I Studniberg *The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Emily M ErikssonThe Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
Suhendro SuwartoDivision of Tropical and Infectious Diseases, Department of Internal Medicine, Faculty of Medicine, Universitas Indonesia, Cipto Mangunkusumo National Hospital (RSCM), Jakarta, Indonesia.
Dionisius DenisEijkman Research Center for Molecular Biology, Jakarta, Indonesia.
Yang LiaoOlivia Newton-John Cancer Research Institute, Heidelberg, VIC, Australia.
Wei ShiOlivia Newton-John Cancer Research Institute, Heidelberg, VIC, Australia.
Alexandra L GarnhamThe Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia.
R Tedjo SasmonoEijkman Research Center for Molecular Biology, Jakarta, Indonesia.
Diana S HansenDepartment of Medical Biology, The University of Melbourne, Parkville, VIC, Australia. diana.hansen@monash.edu.ORCID http://orcid.org/0000-0003-4511-7918
The University of Melbourne · AUEijkman Institute for Molecular Biology · IDOlivia Newton-John Cancer Wellness & Research Centre · AUUniversity of Indonesia · ID

Funding

Australian Academy of Science Regional Collaboration GrantMinistry of Research and Technology of Indonesia Ministry of Research and Technology of IndonesiaNational Health and Medical Research Council 200466National Health and Medical Research Council Independent Medical Research Institutes Infrastructure Support Scheme
6 · The paper itself

Abstract

backgroundTypical symptoms of uncomplicated dengue fever (DF) include headache, muscle pains, rash, cough, and vomiting. A proportion of cases progress to severe dengue hemorrhagic fever (DHF), associated with increased vascular permeability, thrombocytopenia, and hemorrhages. Progression to severe dengue is difficult to diagnose at the onset of fever, which complicates patient triage, posing a socio-economic burden on health systems.

methodsTo identify parameters associated with protection and susceptibility to DHF, we pursued a systems immunology approach integrating plasma chemokine profiling, high-dimensional mass cytometry and peripheral blood mononuclear cell (PBMC) transcriptomic analysis at the onset of fever in a prospective study conducted in Indonesia.

resultsAfter a secondary infection, progression to uncomplicated dengue featured transcriptional profiles associated with increased cell proliferation and metabolism, and an expansion of ICOS

conclusionsOur results suggests that effector memory T cell activation might play an important role ameliorating severe disease symptoms during a secondary dengue infection, and in the absence of that response, a strong innate inflammatory response is required to control viral replication. Our research also identified discrete cell populations predicting increased odds of severe disease, with potential diagnostic value.

Indexed as

DengueSevere DengueHumansLeukocytes, MononuclearProspective StudiesT-LymphocytesDengue feverDengue hemorrhagic feverEffector memory T cellsNon-classical monocytes

Identifiers

PMID37055751
PMCPMC10103532
OpenAlexW4365450678

What OpenQuestion holds

Textmetadata
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.