Evidence map›Paper›PMID 28283425›Full record

ArticleEBioMedicine2017

A Rapid Zika Diagnostic Assay to Measure Neutralizing Antibodies in Patients.

Chao Shan, Xuping Xie, Ping Ren, Michael J Loeffelholz, Yujiao Yang, Andrea Furuya, Alan P Dupuis, Laura D Kramer, Susan J Wong, Pei-Yong Shi

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
11.4field-weighted citation impact, top 1% 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

45 citing papers in PubMed, 65 citations in OpenAlex.

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  12. Zika virus serological diagnosis: commercial tests and monoclonal antibodies as tools.The journal of venomous animals and toxins including tropical diseases · 2020
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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 1 country.

Chao ShanDepartment of Biochemistry & Molecular Biology, University of Texas Medical Branch, Galveston, TX, USA.
Xuping XieDepartment of Biochemistry & Molecular Biology, University of Texas Medical Branch, Galveston, TX, USA.
Ping RenDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, USA.
Michael J LoeffelholzDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, USA.
Yujiao YangDepartment of Biochemistry & Molecular Biology, University of Texas Medical Branch, Galveston, TX, USA.
Andrea FuruyaWadsworth Center, New York State Department of Health, Albany, NY, USA.
Alan P DupuisWadsworth Center, New York State Department of Health, Albany, NY, USA.
Laura D KramerWadsworth Center, New York State Department of Health, Albany, NY, USA.
Susan J WongWadsworth Center, New York State Department of Health, Albany, NY, USA.
Pei-Yong ShiDepartment of Biochemistry & Molecular Biology, University of Texas Medical Branch, Galveston, TX, USA; Department of Pharmacology & Toxicology, University of Texas Medical Branch, Galveston, TX, USA; Sealy Center for Structural Biology & Molecular Biophysics, University of Texas Medical Branch, Galveston, TX, USA; Institute for Translational Science, University of Texas Medical Branch, Galveston, TX, USA. Electronic address: peshi@utmb.edu.
The University of Texas Medical Branch at Galveston · USNew York State Department of Health · USWadsworth Center · US

Funding

NCEZID CDC HHS U01 CK000512
6 · The paper itself

Abstract

The potential association of microcephaly and other congenital abnormalities with Zika virus (ZIKV) infection during pregnancy underlines the critical need for a rapid and accurate diagnosis. Due to the short duration of ZIKV viremia in infected patients, a serologic assay that detects antibody responses to viral infection plays an essential role in diagnosing patient specimens. The current serologic diagnosis of ZIKV infection relies heavily on the labor-intensive Plaque Reduction Neutralization Test (PRNT) that requires more than one-week turnaround time and represents a major bottleneck for patient diagnosis. To overcome this limitation, we have developed a high-throughput assay for ZIKV and dengue virus (DENV) diagnosis that can attain the "gold standard" of the current PRNT assay. The new assay is homogeneous and utilizes luciferase viruses to quantify the neutralizing antibody titers in a 96-well format. Using 91 human specimens, we showed that the reporter diagnostic assay has a higher dynamic range and maintains the relative specificity of the traditional PRNT assay. Besides the improvement of assay throughput, the reporter virus technology has also shortened the turnaround time to less than two days. Collectively, our results suggest that, along with the viral RT-PCR assay, the reporter virus-based serologic assay could be potentially used as the first-line test for clinical diagnosis of ZIKV infection as well as for vaccine clinical trials.

Indexed as

AnimalsAntibodies, NeutralizingCell LineChlorocebus aethiopsCricetinaeCricetulusHumansNeutralization TestsReagent Kits, DiagnosticSensitivity and SpecificityVero CellsZika Virus InfectionAntibodies, NeutralizingReagent Kits, DiagnosticDengue virusFlavivirus diagnosisNeutralization assaySerologic assayZika virus

Identifiers

PMID28283425
PMCPMC5360589
OpenAlexW2592799286

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.