Evidence map›Paper›PMID 29556082›Full record

ArticleScientific reports2018

ILF2 and ILF3 are autoantigens in canine systemic autoimmune disease.

Hanna D Bremer, Nils Landegren, Ronald Sjöberg, Åsa Hallgren, Stefanie Renneker, Erik Lattwein, Dag Leonard, Maija-Leena Eloranta, Lars Rönnblom, Gunnel Nordmark and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 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
0.8field-weighted citation impact, top 31% 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, 18 citations in OpenAlex.

  1. Article
  2. Review
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  4. DNA and RNA Binding Proteins: From Motifs to Roles in Cancer.International journal of molecular sciences · 2022
    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

16 authors at 6 institutions in 4 countries.

Hanna D BremerDepartment of Clinical Sciences, Swedish University of Agricultural Sciences, SE-750 07, Uppsala, Sweden. hanna.bremer@slu.se.ORCID 0000-0002-0236-7514
Nils LandegrenDepartment of Medicine Solna, CMM, L8:01, Karolinska University Hospital, Karolinska Institutet, SE-171 76, Stockholm, Sweden.
Ronald SjöbergAffinity Proteomics, SciLifeLab, School of Biotechnology, KTH Royal Institute of Technology, SE-171 21, Solna, Sweden.
Åsa HallgrenDepartment of Medicine Solna, CMM, L8:01, Karolinska University Hospital, Karolinska Institutet, SE-171 76, Stockholm, Sweden.
Stefanie RennekerEuroimmun AG, 23560, Lübeck, Germany.
Erik LattweinEuroimmun AG, 23560, Lübeck, Germany.
Dag LeonardDepartement of Medical Sciences, Rheumatology and Science for Life Laboratory, Uppsala University, SE 751 85, Uppsala, Sweden.
Maija-Leena ElorantaDepartement of Medical Sciences, Rheumatology and Science for Life Laboratory, Uppsala University, SE 751 85, Uppsala, Sweden.
Lars RönnblomDepartement of Medical Sciences, Rheumatology and Science for Life Laboratory, Uppsala University, SE 751 85, Uppsala, Sweden.
Gunnel NordmarkDepartement of Medical Sciences, Rheumatology and Science for Life Laboratory, Uppsala University, SE 751 85, Uppsala, Sweden.ORCID 0000-0002-3829-7431
Peter NilssonAffinity Proteomics, SciLifeLab, School of Biotechnology, KTH Royal Institute of Technology, SE-171 21, Solna, Sweden.
Göran AnderssonDepartment of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, SE-750 07, Uppsala, Sweden.
Inger LilliehöökDepartment of Clinical Sciences, Swedish University of Agricultural Sciences, SE-750 07, Uppsala, Sweden.
Kerstin Lindblad-TohBroad Institute of Harvard and MIT, Cambridge, MA, 02142, USA.
Olle KämpeDepartment of Medicine Solna, CMM, L8:01, Karolinska University Hospital, Karolinska Institutet, SE-171 76, Stockholm, Sweden.ORCID 0000-0001-6091-9914
Helene Hansson-HamlinDepartment of Clinical Sciences, Swedish University of Agricultural Sciences, SE-750 07, Uppsala, Sweden.
Uppsala University · SESwedish University of Agricultural Sciences · SEEuroimmun Medizinische Labordiagnostika (Germany) · DEScience for Life Laboratory · SEBroad Institute · USKarolinska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dogs can spontaneously develop complex systemic autoimmune disorders, with similarities to human autoimmune disease. Autoantibodies directed at self-antigens are a key feature of these autoimmune diseases. Here we report the identification of interleukin enhancer-binding factors 2 and 3 (ILF2 and ILF3) as autoantigens in canine immune-mediated rheumatic disease. The ILF2 autoantibodies were discovered in a small, selected canine cohort through the use of human protein arrays; a method not previously described in dogs. Subsequently, ILF3 autoantibodies were also identified in the same cohort. The results were validated with an independent method in a larger cohort of dogs. ILF2 and ILF3 autoantibodies were found exclusively, and at a high frequency, in dogs that showed a speckled pattern of antinuclear antibodies on immunofluorescence. ILF2 and ILF3 autoantibodies were also found at low frequency in human patients with SLE and Sjögren's syndrome. These autoantibodies have the potential to be used as diagnostic biomarkers for canine, and possibly also human, autoimmune disease.

Indexed as

AnimalsAntibodies, AntinuclearAutoantigensAutoimmune DiseasesDogsHumansNuclear Factor 45 ProteinNuclear Factor 90 ProteinsAntibodies, AntinuclearAutoantigensNuclear Factor 45 ProteinNuclear Factor 90 Proteins

Identifiers

PMID29556082
PMCPMC5859008
OpenAlexW2791680206

What OpenQuestion holds

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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.