Evidence map›Paper›PMID 26657027›Full record

ArticleScientific reports2015

Infectious dengue vesicles derived from CD61+ cells in acute patient plasma exhibited a diaphanous appearance.

Alan Yi-Hui Hsu, Shang-Rung Wu, Jih-Jin Tsai, Po-Lin Chen, Ya-Ping Chen, Tsai-Yun Chen, Yu-Chih Lo, Tzu-Chuan Ho, Meed Lee, Min-Ting Chen and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Plants (Basel, Switzerland) · 2022
    Article
  4. Article
  5. Review
  6. Review
  7. Dengue type 1 viruses circulating in humans are highly infectious and poorly neutralized by human antibodies.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. 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

12 authors.

Alan Yi-Hui HsuDepartment of Microbiology and Immunology, Tainan, Taiwan.
Shang-Rung WuInstitute of Oral Medicine, National Cheng Kung University, Tainan, Taiwan.
Jih-Jin TsaiTropical Medicine Center, Kaohsiung, Taiwan.
Po-Lin ChenDepartment of Internal Medicine, National Cheng Kung University, Tainan, Taiwan.
Ya-Ping ChenDepartment of Internal Medicine, National Cheng Kung University, Tainan, Taiwan.
Tsai-Yun ChenDepartment of Internal Medicine, National Cheng Kung University, Tainan, Taiwan.
Yu-Chih LoCenter of Infectious Disease and Signaling Research, Tainan, Taiwan.
Tzu-Chuan HoDepartment of Microbiology and Immunology, Tainan, Taiwan.
Meed LeeDepartment of Microbiology and Immunology, Tainan, Taiwan.
Min-Ting ChenInstitute of Oral Medicine, National Cheng Kung University, Tainan, Taiwan.
Yen-Chi ChiuInstitute of Oral Medicine, National Cheng Kung University, Tainan, Taiwan.
Guey Chuen PerngDepartment of Microbiology and Immunology, Tainan, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The levels of neutralizing antibody to a pathogen are an effective indicator to predict efficacy of a vaccine in trial. And yet not all the trial vaccines are in line with the theory. Using dengue virus (DENV) to investigate the viral morphology affecting the predictive value, we evaluated the viral morphology in acute dengue plasma compared to that of Vero cells derived DENV. The virions in plasma were infectious and heterogeneous in shape with a "sunny-side up egg" appearance, viral RNA was enclosed with CD61+ cell-derived membrane interspersed by the viral envelope protein, defined as dengue vesicles. The unique viral features were also observed from ex vivo infected human bone marrow. Dengue vesicles were less efficiently neutralized by convalescent patient serum, compared to virions produced from Vero cells. Our results exhibit a reason why potencies of protective immunity fail in vivo and significantly impact dengue vaccine and drug development.

Indexed as

AnimalsBiological TransportBone Marrow CellsCapsid ProteinsCell MembraneChlorocebus aethiopsCytoplasmic VesiclesDengueDengue VirusHumansIntegrin beta3MegakaryocytesPhenotypeSerogroupVero CellsViral LoadCapsid ProteinsIntegrin beta3

Identifiers

PMID26657027
PMCPMC4675971

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.