Evidence map›Paper›PMID 34930943›Full record

ArticleScientific reports2021

The activation fragment of PAR2 is elevated in serum from patients with rheumatoid arthritis and reduced in response to anti-IL6R treatment.

Stefania Kalogera, Yi He, Anne-Christine Bay-Jensen, Thorbjørn Gantzel, Shu Sun, Tina Manon-Jensen, Morten Asser Karsdal, Christian S Thudium

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Understanding phage Receptor-binding protein interaction with host surface receptor: the key for phage-Mediated detection and elimination of Pseudomonas aeruginosa.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
    Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. PARting Neuroinflammation with Protease-Activated Receptor 2 Pepducins.The Journal of pharmacology and experimental therapeutics · 2024
    Article
  9. Article
  10. Article
  11. 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

8 authors at 2 institutions in 1 country.

Stefania KalogeraNordic Bioscience, Immunoscience, Biomarkers and Research, Herlev, Denmark. ska@nordicbio.com.
Yi HeNordic Bioscience, Immunoscience, Biomarkers and Research, Herlev, Denmark.
Anne-Christine Bay-JensenNordic Bioscience, Immunoscience, Biomarkers and Research, Herlev, Denmark.
Thorbjørn GantzelOrthopaedic Surgery Unit, Gentofte University Hospital, Gentofte, Denmark.
Shu SunNordic Bioscience, Immunoscience, Biomarkers and Research, Herlev, Denmark.
Tina Manon-JensenNordic Bioscience, Immunoscience, Biomarkers and Research, Herlev, Denmark.
Morten Asser KarsdalNordic Bioscience, Immunoscience, Biomarkers and Research, Herlev, Denmark.
Christian S ThudiumNordic Bioscience, Immunoscience, Biomarkers and Research, Herlev, Denmark.
Nordic Bioscience (Denmark) · DKGentofte Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis (OA) and rheumatoid arthritis (RA) are serious and painful diseases. Protease-activated receptor 2 (PAR2) is involved in the pathology of both OA and RA including roles in synovial hyperplasia, cartilage destruction, osteophyogenesis and pain. PAR2 is activated via cleavage of its N-terminus by serine proteases. In this study a competitive ELISA assay was developed targeting the 36-amino acid peptide that is cleaved and released after PAR2 activation (PRO-PAR2). Technical assay parameters including antibody specificity, intra- and inter-assay variation (CV%), linearity, accuracy, analyte stability and interference were evaluated. PRO-PAR2 release was confirmed after in vitro cleavage of PAR2 recombinant protein and treatment of human synovial explants with matriptase. Serum levels of 22 healthy individuals, 23 OA patients and 15 RA patients as well as a subset of RA patients treated with tocilizumab were evaluated. The PRO-PAR2 antibody was specific for the neo-epitope and intra-inter assay CV% were 6.4% and 5.8% respectively. In vitro cleavage and matriptase treated explants showed increased PRO-PAR2 levels compared to controls. In serum, PRO-PAR2 levels were increased in RA patients and decreased in RA patients treated with tocilizumab. In conclusion, PRO-PAR2 may be a potential biomarker for monitoring RA disease and pharmacodynamics of treatment.

Indexed as

AdultAgedAntibodiesAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedArthritis, RheumatoidBiomarkersCartilageEpitopesFemaleHumansImmunoassayLinear ModelsMaleMiddle AgedOsteoarthritisAntibodiesAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedBiomarkersEpitopesF2RL1 protein, humanIL6R protein, humanmatriptaseReceptor, PAR-2Receptors, Interleukin-6Serine Endopeptidasestocilizumab

Identifiers

PMID34930943
PMCPMC8688421
OpenAlexW4200051222

What OpenQuestion holds

Textmetadata
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.