Evidence map›Paper›PMID 29361142›Full record

ArticleRheumatology (Oxford, England)2018

Multiple target autoantigens on endothelial cells identified in juvenile dermatomyositis using proteomics.

Rie Karasawa, Mayumi Tamaki, Toshiko Sato, Megumi Tanaka, Makiko Nawa, Kazuo Yudoh, James N Jarvis

Open access · bronzeAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-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.

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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
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  8. Review
  9. Article
  10. Review
  11. Article
  12. The Vasculopathy of Juvenile Dermatomyositis.Frontiers in pediatrics · 2018
    Review
  13. Review
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

7 authors at 3 institutions in 2 countries.

Rie KarasawaDepartment of Frontier Medicine, St Marianna University School of Medicine, Kawasak, Japani.
Mayumi TamakiDepartment of Frontier Medicine, St Marianna University School of Medicine, Kawasak, Japani.
Toshiko SatoDepartment of Frontier Medicine, St Marianna University School of Medicine, Kawasak, Japani.
Megumi TanakaDepartment of Frontier Medicine, St Marianna University School of Medicine, Kawasak, Japani.
Makiko NawaInstitute of Nanken-Kyoten and RCC, Tokyo Medical and Dental University, Tokyo, Japan.
Kazuo YudohDepartment of Frontier Medicine, St Marianna University School of Medicine, Kawasak, Japani.
James N JarvisDepartment of Pediatrics and Genetics, Genomics, & Bioinformatics Program, Jacobs School of Medicine and Biomedical Sciences University at Buffalo, Buffalo, NY, USA.
St. Marianna University School of Medicine · JPPediatrics and Genetics · USTokyo Medical and Dental University · JP

Funding

Microarray-Based Biomarkers in Juvenile Idiopathic ArthritisR01AR060604 · NIAMS · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI JARVIS, JAMES N · 2011 to 2015
$2.6M
NIAMS NIH HHS R01 AR060604
6 · The paper itself

Abstract

Objective: Although generally classified within the group of inflammatory myopathies, JDM displays many pathological features of vasculitis. Previous work has shown that AECA are abundant in other forms of vasculitis. We therefore investigated whether such antibodies might also be detected in JDM. Methods: We screened plasma from children with JDM for the presence of AECA by western blotting and 2D gel electrophoresis (2DE) using proteins extracted from human aortic endothelial cells as the substrate. We performed mass spectrometry to identify candidate antigens from 2DE gels and used ELISA to confirm the presence of specific antibodies. Results: We identified 22 candidate target autoantigens for AECA probed with JDM plasma. Interestingly, 17 of these 22 target antigens were proteins associated with antigen processing and protein trafficking. ELISA confirmed the presence of antibodies to heat shock cognate 71 kDa protein in JDM plasma, particularly in children with active, untreated disease. Conclusion: Children with JDM express antibodies to autoantigens in endothelial cells. The clinical and pathological significance of such autoantibodies require further investigation.

Indexed as

AdolescentAortaAutoantibodiesAutoantigensBiomarkersBiopsyBlotting, WesternCells, CulturedChildChild, PreschoolChromatography, High Pressure LiquidDermatomyositisElectrophoresis, Gel, Two-DimensionalElectrophoresis, Polyacrylamide GelEndothelial CellsEndothelium, VascularAutoantibodiesAutoantigensBiomarkers

Identifiers

PMID29361142
PMCPMC5888918
OpenAlexW2791731016

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.