Evidence map›Paper›PMID 29186193›Full record

ArticlePLoS pathogens2017

RIG-I-like receptor activation by dengue virus drives follicular T helper cell formation and antibody production.

Joris K Sprokholt, Tanja M Kaptein, John L van Hamme, Ronald J Overmars, Sonja I Gringhuis, Teunis B H Geijtenbeek

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

39 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Innate Immune and Inflammatory Responses to Dengue Virus Infection.Current topics in microbiology and immunology · 2026
    Review
  5. T Cell Responses During Dengue Infection.Current topics in microbiology and immunology · 2026
    Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Viruses · 2022
    Review
  17. Review
  18. Review
  19. Innate and adaptive immune evasion by dengue virus.Frontiers in cellular and infection microbiology · 2022
    Review
  20. 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

6 authors at 1 institution in 1 country.

Joris K SprokholtDepartment of Experimental Immunology, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.
Tanja M KapteinDepartment of Experimental Immunology, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.
John L van HammeDepartment of Experimental Immunology, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.
Ronald J OvermarsDepartment of Experimental Immunology, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.
Sonja I GringhuisDepartment of Experimental Immunology, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.
Teunis B H GeijtenbeekDepartment of Experimental Immunology, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0002-5710-2839
Amsterdam UMC Location University of Amsterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Follicular T helper cells (TFH) are fundamental in orchestrating effective antibody-mediated responses critical for immunity against viral infections and effective vaccines. However, it is unclear how virus infection leads to TFH induction. We here show that dengue virus (DENV) infection of human dendritic cells (DCs) drives TFH formation via crosstalk of RIG-I-like receptor (RLR) RIG-I and MDA5 with type I Interferon (IFN) signaling. DENV infection leads to RLR-dependent IKKε activation, which phosphorylates IFNα/β receptor-induced STAT1 to drive IL-27 production via the transcriptional complex ISGF3. Inhibiting RLR activation as well as neutralizing antibodies against IL-27 prevented TFH formation. DENV-induced CXCR5+PD-1+Bcl-6+ TFH cells secreted IL-21 and activated B cells to produce IgM and IgG. Notably, RLR activation by synthetic ligands also induced IL-27 secretion and TFH polarization. These results identify an innate mechanism by which antibodies develop during viral disease and identify RLR ligands as potent adjuvants for TFH-promoting vaccination strategies.

Indexed as

Antibodies, ViralAntibody FormationB-LymphocytesDEAD Box Protein 58Dendritic CellsDengueDengue VirusHumansInterferon-Induced Helicase, IFIH1Interleukin-21Interleukin-27InterleukinsLymphocyte ActivationReceptors, ImmunologicT-Lymphocytes, Helper-InducerAntibodies, ViralDEAD Box Protein 58IFIH1 protein, humanInterferon-Induced Helicase, IFIH1Interleukin-21Interleukin-27InterleukinsReceptors, ImmunologicRIGI protein, human

Identifiers

PMID29186193
PMCPMC5724900
OpenAlexW2770345881

What OpenQuestion holds

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LicenceCC BY
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.