Evidence map›Paper›PMID 29623076›Full record

ArticleFrontiers in immunology2018

Autoantibodies in Serum of Systemic Scleroderma Patients: Peptide-Based Epitope Mapping Indicates Increased Binding to Cytoplasmic Domains of CXCR3.

Andreas Recke, Ann-Katrin Regensburger, Florian Weigold, Antje Müller, Harald Heidecke, Gabriele Marschner, Christoph M Hammers, Ralf J Ludwig, Gabriela Riemekasten

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Observational
  2. Olink proteomics and lipidomics analysis of serum from patients infected with non-tuberculous mycobacteria and Mycobacterium tuberculosis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Article
  3. Review
  4. Review
  5. Review
  6. A broad look into the future of systemic sclerosis.Therapeutic advances in musculoskeletal disease · 2022
    Review
  7. Review
  8. Review
  9. Article
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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

9 authors at 4 institutions in 1 country.

Andreas ReckeDepartment of Dermatology, University of Lübeck, Lübeck, Germany.
Ann-Katrin RegensburgerLübeck Institute of Dermatological Research, University of Lübeck, Lübeck, Germany.
Florian WeigoldDepartment of Rheumatology and Clinical Immunology, Charité University Hospital, Berlin, Germany.
Antje MüllerDepartment of Rheumatology, University of Lübeck, Lübeck, Germany.
Harald HeideckeCellTrend GmbH, Luckenwalde, Germany.
Gabriele MarschnerDepartment of Rheumatology, University of Lübeck, Lübeck, Germany.
Christoph M HammersDepartment of Dermatology, University of Lübeck, Lübeck, Germany.
Ralf J LudwigLübeck Institute of Dermatological Research, University of Lübeck, Lübeck, Germany.
Gabriela RiemekastenDepartment of Rheumatology, University of Lübeck, Lübeck, Germany.
University of Lübeck · DECharité - Universitätsmedizin Berlin · DEGerman Center for Lung Research · DEInstitute of Pathology Celle · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic sclerosis (SSc) is a severe chronic autoimmune disease with high morbidity and mortality. Sera of patients with SSc contain a large variety of autoantibody (aab) reactivities. Among these are functionally active aab that bind to G protein-coupled receptors (GPCR) such as C-X-C motif chemokine receptor 3 (CXCR3) and 4 (CXCR4). Aab binding to the N-terminal portion of these two GPCRs have been shown to be associated with slower disease progression in SSc, especially deterioration of lung function. Aabs binding to GPCRs exhibit functional activities by stimulating or inhibiting GPCR signaling. The specific functional activity of aabs crucially depends on the epitopes they bind to. To identify the location of important epitopes on CXCR3 recognized by aabs from SSc patients, we applied an array of 36 overlapping 18-20mer peptides covering the entire CXCR3 sequence, comparing epitope specificity of SSc patient sera (

Indexed as

AdultAgedAutoantibodiesComputational BiologyCytoplasmEnzyme-Linked Immunosorbent AssayEpitope MappingEpitopes, B-LymphocyteFemaleHumansMaleMiddle AgedMonitoring, PhysiologicPeptidesProtein BindingProtein DomainsAutoantibodiesCXCR3 protein, humanEpitopes, B-LymphocytePeptidesReceptors, CXCR3autoantibodiesCXCR3G protein-coupled receptorpeptide arraysystemic sclerosis

Identifiers

PMID29623076
PMCPMC5874968
OpenAlexW2793817186

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.