Evidence map›Paper›PMID 34504485›Full record

ArticleFrontiers in immunology2021

Elevated Fibronectin Levels in Profibrotic CD14

Michał Rudnik, Amela Hukara, Ievgeniia Kocherova, Suzana Jordan, Janine Schniering, Vincent Milleret, Martin Ehrbar, Karin Klingel, Carol Feghali-Bostwick, Oliver Distler and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

41 citing papers in PubMed, 53 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

12 authors at 4 institutions in 4 countries.

Michał RudnikDepartment of Rheumatology, Center of Experimental Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Amela HukaraDepartment of Rheumatology, Center of Experimental Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Ievgeniia KocherovaDepartment of Rheumatology, Center of Experimental Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Suzana JordanDepartment of Rheumatology, Center of Experimental Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Janine SchnieringDepartment of Rheumatology, Center of Experimental Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Vincent MilleretDepartment of Obstetrics, University Hospital Zurich, Zurich, Switzerland.
Martin EhrbarDepartment of Obstetrics, University Hospital Zurich, Zurich, Switzerland.
Karin KlingelDepartment of Molecular Pathology, University Hospital Tuebingen, Tuebingen, Germany.
Carol Feghali-BostwickDivision of Rheumatology, Medical University of South Carolina, Charleston, SC, United States.
Oliver DistlerDepartment of Rheumatology, Center of Experimental Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Przemysław BłyszczukDepartment of Rheumatology, Center of Experimental Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Gabriela KaniaDepartment of Rheumatology, Center of Experimental Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
University Hospital of Zurich · CHUniversity of Zurich · CHMedical University of South Carolina · USUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Systemic sclerosis (SSc) is an autoimmune disease characterized by overproduction of extracellular matrix (ECM) and multiorgan fibrosis. Animal studies pointed to bone marrow-derived cells as a potential source of pathological ECM-producing cells in immunofibrotic disorders. So far, involvement of monocytes and macrophages in the fibrogenesis of SSc remains poorly understood. Methods and Results: Immunohistochemistry analysis showed accumulation of CD14 Conclusions: Our findings identified activated profibrotic signature with elevated production of profibrotic fibronectin in CD14

Indexed as

AdultAgedBiomarkersCase-Control StudiesCell DifferentiationCytokinesDisease SusceptibilityFemaleFibroblastsFibronectinsHumansLipopolysaccharide ReceptorsMacrophagesMaleMiddle AgedMonocytesBiomarkersCytokinesFibronectinsLipopolysaccharide ReceptorsTransforming Growth Factor betaCD14+ macrophagesCD14+ monocytesfibronectinfibrosissystemic sclerosisTGF-β

Identifiers

PMID34504485
PMCPMC8421541
OpenAlexW3195818601

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.