Evidence map›Paper›PMID 28791018›Full record

ArticleFrontiers in immunology2017

Genetic and Functional Associations with Decreased Anti-inflammatory Tumor Necrosis Factor Alpha Induced Protein 3 in Macrophages from Subjects with Axial Spondyloarthritis.

Yiping Liu, Zhan Ye, Xiang Li, Jennifer L Anderson, Mike Khan, Douglas DaSilva, Marissa Baron, Deborah Wilson, Vera Bocoun, Lynn C Ivacic and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Multicellular network analysis of melanoma heterogeneity by scRNA-seq.American journal of translational research · 2023
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  3. Review
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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 3 institutions in 1 country.

Yiping LiuDepartment of Pediatrics, University of Wisconsin-Madison, Madison, WI, United States.
Zhan YeBiomedical Informatics Research Center, Marshfield Clinic Research Institute, Marshfield, WI, United States.
Xiang LiBiomedical Informatics Research Center, Marshfield Clinic Research Institute, Marshfield, WI, United States.
Jennifer L AndersonIntegrated Research and Development Laboratory, Marshfield Clinic Research Institute, Marshfield, WI, United States.
Mike KhanDepartment of Pathology and Laboratory Medicine, University of Wisconsin-Madison School of Medicine and Public Health, Madison, WI, United States.
Douglas DaSilvaDepartment of Pediatrics, University of Wisconsin-Madison, Madison, WI, United States.
Marissa BaronGraduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States.
Deborah WilsonDepartment of Rheumatology, Marshfield Clinic, Marshfield, WI, United States.
Vera BocounDepartment of Rheumatology, Marshfield Clinic, Marshfield, WI, United States.
Lynn C IvacicIntegrated Research and Development Laboratory, Marshfield Clinic Research Institute, Marshfield, WI, United States.
Steven J SchrodiCenter for Human Genetics, Marshfield Clinic Research Institute, Marshfield, WI, United States.
Judith A SmithDepartment of Pediatrics, University of Wisconsin-Madison, Madison, WI, United States.
Marshfield Clinic · USUniversity of Wisconsin–Madison · USUniversity of Pittsburgh · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTumor necrosis factor alpha-induced protein 3 (TNFAIP3) is an anti-inflammatory protein implicated in multiple autoimmune and rheumatologic conditions. We hypothesized that lower levels of TNFAIP3 contributes to excessive cytokine production in response to inflammatory stimuli in axial spondyloarthritis (AxSpA). A further aim was to determine the immune signaling and genetic variation regulating TNFAIP3 expression in individual subjects.

methodsBlood-derived macrophages from 50 AxSpA subjects and 30 healthy controls were assessed for TNFAIP3 expression. Cell lysates were also analyzed for NF-κB, mitogen-activated protein (MAP) kinase and STAT3 phosphorylation, and supernatants for cytokine production. Coding and regulatory regions in the

resultsMean TNFAIP3 was significantly lower in spondyloarthritis macrophages than controls (

conclusionOur results suggest that both immune functional and genetic variations contribute to the regulation of TNFAIP3 levels in individual subjects. Decreased expression of TNFAIP3 in AxSpA macrophages correlated with increased LPS-induced TNF-α, and thus, TNFAIP3 dysregulation may be a contributor to excessive inflammatory responses in spondyloarthritis subjects.

Indexed as

cytokine productiongenetic variantsmacrophagesspondyloarthritisspondyloarthritis pathogenesisTNF-αtumor necrosis factor alpha-induced protein 3

Identifiers

PMID28791018
PMCPMC5523649
OpenAlexW2736502755

What OpenQuestion holds

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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.