Evidence map›Paper›PMID 33976375›Full record

ArticleCommunications biology2021

Dengue virus-free defective interfering particles have potent and broad anti-dengue virus activity.

Dongsheng Li, Min-Hsuan Lin, Daniel J Rawle, Hongping Jin, Zhonglan Wu, Lu Wang, Mary Lor, Mazhar Hussain, John Aaskov, David Harrich

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

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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 2 countries.

Dongsheng Li *Department of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Min-Hsuan Lin *Department of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Daniel J RawleDepartment of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.ORCID http://orcid.org/0000-0001-7248-0101
Hongping JinDepartment of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Zhonglan WuNingxia Center for Disease Control and Prevention, Ningxia, China.
Lu WangDepartment of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Mary LorDepartment of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Mazhar HussainInstitute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, QLD, Australia.
John AaskovInstitute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, QLD, Australia.
David HarrichDepartment of Cell and Molecular Biology, QIMR Berghofer Medical Research Institute, Herston, QLD, Australia. David.Harrich@qimrberghofer.edu.au.ORCID http://orcid.org/0000-0003-3690-0150
QIMR Berghofer Medical Research Institute · AUQueensland University of Technology · AUNingxia Center for Diseases Prevention and Control · CN

Funding

Wellcome Trust
6 · The paper itself

Abstract

Dengue virus (DENV) is spread from human to human through the bite of the female Aedes aegypti mosquito and leads to about 100 million clinical infections yearly. Treatment options and vaccine availability for DENV are limited. Defective interfering particles (DIPs) are considered a promising antiviral approach but infectious virus contamination has limited their development. Here, a DENV-derived DIP production cell line was developed that continuously produced DENV-free DIPs. The DIPs contained and could deliver to cells a DENV serotype 2 subgenomic defective-interfering RNA, which was originally discovered in DENV infected patients. The DIPs released into cell culture supernatant were purified and could potently inhibit replication of all DENV serotypes in cells. Antiviral therapeutics are limited for many viral infection. The DIP system described could be re-purposed to make antiviral DIPs for many other RNA viruses such as SARS-CoV-2, yellow fever, West Nile and Zika viruses.

Indexed as

Defective VirusesVirus ReplicationAnimalsCell Line, TumorChlorocebus aethiopsDengueDengue VaccinesDengue VirusGenes, ReporterHEK293 CellsHost-Pathogen InteractionsHumansLuminescent ProteinsRNA, ViralVero CellsViral LoadDengue VaccinesLuminescent ProteinsRNA, Viral

Identifiers

PMID33976375
PMCPMC8113447
OpenAlexW3160337431

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.