Evidence map›Paper›PMID 30177933›Full record

ArticleFrontiers in immunology2018

The

Niloufar Kavian, Souad Mehlal, Mohamed Jeljeli, Nathaniel Edward Bennett Saidu, Carole Nicco, Olivier Cerles, Sandrine Chouzenoux, Anne Cauvet, Claire Camus, Mehdi Ait-Djoudi and 4 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

48 citing papers in PubMed, 116 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 1 country.

Niloufar KavianLaboratoire d'Immunologie, Hôpital Cochin, Paris, France.
Souad MehlalLaboratoire d'Immunologie, Hôpital Cochin, Paris, France.
Mohamed JeljeliLaboratoire d'Immunologie, Hôpital Cochin, Paris, France.
Nathaniel Edward Bennett SaiduINSERM U1016, Institut Cochin, Paris, France.
Carole NiccoINSERM U1016, Institut Cochin, Paris, France.
Olivier CerlesINSERM U1016, Institut Cochin, Paris, France.
Sandrine ChouzenouxINSERM U1016, Institut Cochin, Paris, France.
Anne CauvetINSERM U1016, Institut Cochin, Paris, France.
Claire CamusINSERM U1016, Institut Cochin, Paris, France.
Mehdi Ait-DjoudiINSERM U1016, Institut Cochin, Paris, France.
Christiane ChéreauINSERM U1016, Institut Cochin, Paris, France.
Saadia Kerdine-RömerUMR996 - Inflammation, Chemokines and Immunopathology, INSERM, Univ Paris-Sud, Université Paris-Saclay, Châtenay-Malabry, France.
Yannick AllanoreINSERM U1016, Institut Cochin, Paris, France.
Frederic BatteuxLaboratoire d'Immunologie, Hôpital Cochin, Paris, France.
Inserm · FRAssistance Publique – Hôpitaux de Paris · FRInstitut Cochin · FRUniversité Paris-Saclay · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic sclerosis (SSc) is an autoimmune disease with fibrosis of the skin and internal organs and vascular alterations. Dysregulations in the oxidant/antioxidant balance are known to be a major factor in the pathogenesis of the disease. Indeed, reactive oxygen species (ROS) trigger neoepitopes leading to a breach of immune tolerance and autoimmune responses, activate fibroblasts to proliferate and to produce excess of type I collagen. ROS also alter endothelial cells leading to vascular dysfunction. Glutathione (GSH) is the most potent antioxidant system in eukaryotic cells. Numerous studies have reported a defect in GSH in SSc animal models and humans, but the origin of this defect remains unknown. The transcription factor NRF2 is a key player in the antioxidant defense, as it can induce the transcription of antioxidant and cytoprotective genes, including GSH, through its interaction with the antioxidant response elements. In this work, we investigated whether NRF2 could be implicated in the pathogenesis of SSc, and if this pathway could represent a new therapeutic target in this orphan disease with no curative medicine. Skin biopsies from 11 patients and 10 controls were harvested, and skin fibroblasts were extracted. Experimental SSc was induced both in BALB/c and in

Indexed as

Antioxidant Response ElementsAutoimmunitySignal TransductionAdolescentAdultAgedAnimalsCase-Control StudiesCytokinesDisease Models, AnimalEndothelial CellsFemaleFibroblastsFibrosisGlutathioneHumansCytokinesGlutathioneHydrogen PeroxideInflammation MediatorsNF-E2-Related Factor 2Reactive Oxygen SpeciesfibrosisinflammationNrf2oxidative stresssystemic sclerosis

Identifiers

PMID30177933
PMCPMC6109691
OpenAlexW2885429255

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.