Evidence map›Paper›PMID 37200264›Full record

ArticlePloS one2023

A nonstructural protein 1 capture enzyme-linked immunosorbent assay specific for dengue viruses.

Pei-Yin Lim, Appanna Ramapraba, Thomas Loy, Angeline Rouers, Tun-Linn Thein, Yee-Sin Leo, Dennis R Burton, Katja Fink, Cheng-I Wang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

9 authors at 3 institutions in 2 countries.

Pei-Yin LimSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.ORCID 0000-0003-4401-1265
Appanna RamaprabaSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Thomas LoySingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Angeline RouersSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Tun-Linn TheinNational Centre for Infectious Diseases, Singapore, Singapore.
Yee-Sin LeoNational Centre for Infectious Diseases, Singapore, Singapore.
Dennis R BurtonDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, United States of America.
Katja FinkSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Cheng-I WangSingapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
Agency for Science, Technology and Research · SGNational Centre for Infectious Diseases · SGScripps Research Institute · US

Funding

Resource for Biocomputing Visualization and InformaticsP41GM103311 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FERRIN, THOMAS E · 2012 to 2017
$8.2M
NIGMS NIH HHS P41 GM103311
6 · The paper itself

Abstract

Dengue non-structural protein (NS1) is an important diagnostic marker during the acute phase of infection. Because NS1 is partially conserved across the flaviviruses, a highly specific DENV NS-1 diagnostic test is needed to differentiate dengue infection from Zika virus (ZIKV) infection. In this study, we characterized three newly isolated antibodies against NS1 (A2, D6 and D8) from a dengue-infected patient and a previously published human anti-NS1 antibody (Den3). All four antibodies recognized multimeric forms of NS1 from different serotypes. A2 bound to NS1 from DENV-1, -2, and -3, D6 bound to NS1 from DENV-1, -2, and -4, and D8 and Den3 interacted with NS1 from all four dengue serotypes. Using a competition ELISA, we found that A2 and D6 bound to overlapping epitopes on NS1 whereas D8 recognized an epitope distinct from A2 and D6. In addition, we developed a capture ELISA that specifically detected NS1 from dengue viruses, but not ZIKV, using Den3 as the capture antibody and D8 as the detecting antibody. This assay detected NS1 from all the tested dengue virus strains and dengue-infected patients. In conclusion, we established a dengue-specific capture ELISA using human antibodies against NS1. This assay has the potential to be developed as a point-of-care diagnostic tool.

Indexed as

DengueDengue VirusZika VirusZika Virus InfectionAntibodies, ViralCross ReactionsEnzyme-Linked Immunosorbent AssayEpitopesHumansSensitivity and SpecificityViral Nonstructural ProteinsAntibodies, ViralEpitopesViral Nonstructural Proteins

Identifiers

PMID37200264
PMCPMC10194908
OpenAlexW4377093213

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.