Evidence map›Paper›PMID 26090498›Full record

ArticleJournal of immunology research2015

Characterization of CD30/CD30L(+) Cells in Peripheral Blood and Synovial Fluid of Patients with Rheumatoid Arthritis.

Alessandro Barbieri, Marzia Dolcino, Elisa Tinazzi, Antonella Rigo, Giuseppe Argentino, Giuseppe Patuzzo, Andrea Ottria, Ruggero Beri, Antonio Puccetti, Claudio Lunardi

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 26% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  5. Activation of the proton-sensing GPCR, GPR65 on fibroblast-like synoviocytes contributes to inflammatory joint pain.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  12. Genetic Variants inFrontiers in genetics · 2021
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  16. Antibody-Based Tracers for PET/SPECT Imaging of Chronic Inflammatory Diseases.Chembiochem : a European journal of chemical biology · 2019
    Review
  17. Review
  18. Associations betweenOncotarget · 2017
    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

10 authors at 3 institutions in 1 country.

Alessandro BarbieriDepartment of Medicine, University of Verona, 37134 Verona, Italy.ORCID 0000-0002-4780-5557
Marzia DolcinoInstitute G. Gaslini, 16147 Genova, Italy.
Elisa TinazziDepartment of Medicine, University of Verona, 37134 Verona, Italy.
Antonella RigoDepartment of Medicine, University of Verona, 37134 Verona, Italy.
Giuseppe ArgentinoDepartment of Medicine, University of Verona, 37134 Verona, Italy.
Giuseppe PatuzzoDepartment of Medicine, University of Verona, 37134 Verona, Italy.
Andrea OttriaUniversity of Genova, 16132 Genova, Italy.ORCID 0000-0001-8722-3968
Ruggero BeriDepartment of Medicine, University of Verona, 37134 Verona, Italy.
Antonio PuccettiInstitute G. Gaslini, 16147 Genova, Italy ; University of Genova, 16132 Genova, Italy.
Claudio LunardiDepartment of Medicine, University of Verona, 37134 Verona, Italy.ORCID 0000-0001-6446-2990
University of Verona · ITIstituto Giannina Gaslini · ITUniversity of Genoa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CD30/CD30L signalling system has been implicated in the pathogenesis of several autoimmune and inflammatory conditions. In rheumatoid arthritis (RA), soluble CD30 (sCD30) levels reflect the recruitment of CD30(+) T cells into the inflamed joints and correlate with a positive response to immunosuppressive therapy. The aim of our report was to clarify the role of CD30/CD30L signalling system in the pathogenesis of RA. Our analysis of the CD30L(+) T cell subsets in peripheral blood (PB) and synovial fluid (SF) of RA patients and of the related cytokine profiles suggests the involvement of CD30/CD30L signalling in polarization of T cells towards a Th17 phenotype with proinflammatory features. Moreover, in RA SF nearly 50% of Treg cells express CD30, probably as an attempt to downmodulate the ongoing inflammation. We also show here that the engagement of CD30L on neutrophils stimulated with CD30/Fc chimera may play a crucial role in RA inflammation since activated neutrophils release IL-8, thus potentially amplifying the local inflammatory damage. In conclusion, the results obtained suggest that the complex CD30/CD30L signalling pathway is implicated in the pathogenesis and progression of RA synovitis through a concerted action on several immune effector cells.

Indexed as

Arthritis, RheumatoidCD30 LigandFemaleHumansInflammationInterleukin-8Ki-1 AntigenMaleMiddle AgedNeutrophilsSignal TransductionSynovial FluidTh17 CellsT-Lymphocytes, RegulatoryCD30 LigandInterleukin-8Ki-1 AntigenTNFSF8 protein, human

Identifiers

PMID26090498
PMCPMC4452350
OpenAlexW1485519097

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.