Evidence map›Paper›PMID 28877177›Full record

ArticlePloS one2017

An in vitro diagnostic certified point of care single nucleotide test for IL28B polymorphisms.

Darragh Duffy, Estelle Mottez, Shaun Ainsworth, Tan-Phuc Buivan, Aurelie Baudin, Muriel Vray, Ben Reed, Arnaud Fontanet, Alexandra Rohel, Ventzislava Petrov-Sanchez and 5 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04029454 (Neovac 2 Burkina Faso), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 22% 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.

NCT04029454 nacompletednot on this mapstarted 2020, after this paper: background citation

Neovac 2 Burkina Faso: Impact of the Integration of Hepatitis B Birth Dose Vaccine Into the Infant Immunization Schedule: a Mixed Methods Study Including a Cluster-randomized Trial, an Anthropological Study and an Economic Evaluation

TypeinterventionalSponsorInstitut PasteurRan2020 to 2023Enrolled10,000ConditionsHepatitis BArmsbirth dose vaccination against hepatitis B strategy
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2023
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  3. Article
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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

15 authors at 5 institutions in 3 countries.

Darragh DuffyImmunobiology of Dendritic Cells, Institut Pasteur, Paris, France.ORCID http://orcid.org/0000-0002-8875-2308
Estelle MottezCentre for Translational Research, Institut Pasteur, Paris, France.
Shaun AinsworthGenedrive plc, Manchester, United Kingdom.
Tan-Phuc BuivanCentre for Translational Research, Institut Pasteur, Paris, France.
Aurelie BaudinUniversité Paris Descartes et Département d'hépatologie, Groupe Hospitalier Cochin Hôtel- Dieu, Paris, France.
Muriel VrayEmerging Disease Epidemiology Unit, Institut Pasteur, Paris, France.
Ben ReedGenedrive plc, Manchester, United Kingdom.
Arnaud FontanetEmerging Disease Epidemiology Unit, Institut Pasteur, Paris, France.
Alexandra RohelANRS (France REcherche Nord&Sud Sida-hiv Hépatites), Paris, France.
Ventzislava Petrov-SanchezANRS (France REcherche Nord&Sud Sida-hiv Hépatites), Paris, France.
Laurent AbelLaboratory of Human Genetics of Infectious Diseases, Necker Branch, Inserm U1163, Paris, France.
Ioannis TheodorouDepartment of Immunology, AP-HP, La Pitie Salpetriere, Paris, France.
Gino MieleGenedrive plc, Manchester, United Kingdom.
Stanislas PolImmunobiology of Dendritic Cells, Institut Pasteur, Paris, France.
Matthew L AlbertImmunobiology of Dendritic Cells, Institut Pasteur, Paris, France.
Inserm · FRAgence Nationale de Recherches sur le Sida et les Hépatites Virales · FRConservatoire National des Arts et Métiers · FRSorbonne Université · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Numerous genetic polymorphisms have been identified as associated with disease or treatment outcome, but the routine implementation of genotyping into actionable medical care remains limited. Point-of-care (PoC) technologies enable rapid and real-time treatment decisions, with great potential for extending molecular diagnostic approaches to settings with limited medical infrastructure (e.g., CLIA certified diagnostic laboratories). With respect to resource-limited settings, there is a need for simple devices to implement biomarker guided treatment strategies. One relevant example is chronic hepatitis C infection, for which several treatment options are now approved. Single nucleotide polymorphisms (SNPs) in the IL-28B / IFNL3 locus have been well described to predict both spontaneous clearance and response to interferon based therapies. We utilized the Genedrive® platform to develop an assay for the SNP rs12979860 variants (CC, CT and TT). The assay utilizes a hybrid thermal engine, permitting rapid heating and cooling, enabling an amplification based assay with genetic variants reported using endpoint differential melting cure analysis in less than 60 minutes. We validated this assay using non-invasive buccal swab sampling in a prospective study of 246 chronic HCV patients, achieving 100% sensitivity and 100% specificity (95% exact CI: 98.8-100%)) in 50 minutes as compared to conventional lab based PCR testing. Our results provide proof of concept that precision medicine is feasible in resource-limited settings, offering the first CE-IVD (in vitro diagnostics) validated PoC SNP test. We propose that IL-28B genotyping may be useful for directing patients towards lower cost therapies, and rationing use of costly direct antivirals for use in those individuals showing genetic risk.

Indexed as

Point-of-Care SystemsAdultAgedAged, 80 and overDemographyFemaleHepatitis C, ChronicHumansInterferon LambdaInterferonsInterleukinsMaleMiddle AgedPolymorphism, Single NucleotideReproducibility of ResultsYoung AdultInterferon Lambdainterferon-lambda, humanInterferonsInterleukins

Identifiers

PMID28877177
PMCPMC5587232
OpenAlexW2753159425

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.