Evidence map›Paper›PMID 31533998›Full record

ArticlemSphere2019

Antibody-Dependent Dengue Virus Entry Modulates Cell Intrinsic Responses for Enhanced Infection.

Candice Y Y Chan, John Zhong Heng Low, Esther Shuyi Gan, Eugenia Ziying Ong, Summer Li-Xin Zhang, Hwee Cheng Tan, Xiaoran Chai, Sujoy Ghosh, Eng Eong Ooi, Kuan Rong Chan

Open access · goldAbstract read
In one paragraph

Article in mSphere, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.1field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Dengue and severe dengue.Clinical microbiology reviews · 2025
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Observational
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Intra-Host Diversity of Dengue Virus in Mosquito Vectors.Frontiers in cellular and infection microbiology · 2022
    Review
  18. [Dengue virus E protein-based luciferase immunosorbent assay for detecting dengue virus IgG antibody].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2021
    Article
  19. 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

10 authors at 3 institutions in 1 country.

Candice Y Y ChanProgram in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.
John Zhong Heng LowProgram in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.
Esther Shuyi GanProgram in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.
Eugenia Ziying OngProgram in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.
Summer Li-Xin ZhangProgram in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.
Hwee Cheng TanProgram in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.
Xiaoran ChaiProgram in Cardiovascular & Metabolic Disorders, Duke-NUS Medical School, Singapore.
Sujoy GhoshProgram in Cardiovascular & Metabolic Disorders, Duke-NUS Medical School, Singapore.
Eng Eong OoiProgram in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.
Kuan Rong ChanProgram in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore kuanrong.chan@duke-nus.edu.sg.ORCID 0000-0002-2427-671X
Duke-NUS Medical School · SGNational University of Singapore · SGSingapore General Hospital · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dengue is caused by infection with any one of four dengue viruses (DENV); the risk of severe disease appears to be enhanced by the cross-reactive or subneutralizing levels of antibody from a prior DENV infection. These antibodies opsonize DENV entry through the activating Fc gamma receptors (FcγR), instead of infection through canonical receptor-mediated endocytosis, to result in higher levels of DENV replication. However, whether the enhanced replication is solely due to more efficient FcγR-mediated DENV entry or is also through FcγR-mediated alteration of the host transcriptome response to favor DENV infection remains unclear. Indeed, more efficient viral entry through activation of the FcγR can result in an increased viral antigenic load within target cells and confound direct comparisons of the host transcriptome response under antibody-dependent and antibody-independent conditions. Herein, we show that, despite controlling for the viral antigenic load in primary monocytes, the antibody-dependent and non-antibody-dependent routes of DENV entry induce transcriptome responses that are remarkably different. Notably, antibody-dependent DENV entry upregulated DENV host dependency factors associated with RNA splicing, mitochondrial respiratory chain complexes, and vesicle trafficking. Additionally, supporting findings from other studies, antibody-dependent DENV entry impeded the downregulation of ribosomal genes caused by canonical receptor-mediated endocytosis to increase viral translation. Collectively, our findings support the notion that antibody-dependent DENV entry alters host responses that support the viral life cycle and that host responses to DENV need to be defined in the context of its entry pathway.

Indexed as

Host Microbial InteractionsVirus InternalizationAntibodies, ViralAntibody-Dependent EnhancementAntigens, ViralCell LineCells, CulturedDengueDengue VirusHumansMonocytesReceptors, IgGSequence Analysis, RNATranscriptomeVirus ReplicationAntibodies, ViralAntigens, ViralReceptors, IgGdengue virushost responsevirus-host interactions

Identifiers

PMID31533998
PMCPMC6751492
OpenAlexW2974230966

What OpenQuestion holds

Textmetadata
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.