Evidence map›Paper›PMID 27893701›Full record

ArticleNature immunology2017

The signaling adaptor TRAF1 negatively regulates Toll-like receptor signaling and this underlies its role in rheumatic disease.

Ali A Abdul-Sater, Maria I Edilova, Derek L Clouthier, Achire Mbanwi, Elisabeth Kremmer, Tania H Watts

Abstract read
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In one paragraph

Article in Nature immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

47 citing papers in PubMed, 76 citations in OpenAlex.

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  15. cFLIPCellular & molecular immunology · 2023
    Article
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  18. NMolecular cancer · 2022
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Ali A Abdul-SaterDepartment of Immunology, University of Toronto, Toronto, Ontario, Canada.
Maria I EdilovaDepartment of Immunology, University of Toronto, Toronto, Ontario, Canada.
Derek L ClouthierDepartment of Immunology, University of Toronto, Toronto, Ontario, Canada.
Achire MbanwiDepartment of Immunology, University of Toronto, Toronto, Ontario, Canada.
Elisabeth KremmerInstitut für Molekulare Immunologie, Deutsches Forschungszentrum für Gesundheit und Umwelt (GmbH), München, Germany.
Tania H WattsDepartment of Immunology, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0001-7897-4890
University of Toronto · CA

Funding

CIHR FDN-143250CIHR MOP-74492
6 · The paper itself

Abstract

TRAF1 is a signaling adaptor known for its role in tumor necrosis factor receptor-induced cell survival. Here we show that monocytes from healthy human subjects with a rheumatoid arthritis-associated single-nucleotide polymorphism (SNP) in the TRAF1 gene express less TRAF1 protein but greater amounts of inflammatory cytokines in response to lipopolysaccharide (LPS). The TRAF1 MATH domain binds directly to three components of the linear ubiquitination (LUBAC) complex, SHARPIN, HOIP and HOIL-1, to interfere with the recruitment and linear ubiquitination of NEMO. This results in decreased NF-κB activation and cytokine production, independently of tumor necrosis factor. Consistent with this, Traf1

Indexed as

Signal TransductionAnimalsArthritis, RheumatoidCytokinesGenetic Predisposition to DiseaseHEK293 CellsHumansInflammation MediatorsLeukocytes, MononuclearLipopolysaccharidesMiceMice, Inbred C57BLMice, KnockoutMonocytesPolymorphism, Single NucleotideRNA, Small InterferingCytokinesInflammation MediatorsLipopolysaccharidesRNA, Small InterferingTNF Receptor-Associated Factor 1Toll-Like Receptors

Identifiers

PMID27893701
OpenAlexW2557828008

What OpenQuestion holds

Textmetadata
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.