Evidence map›Paper›PMID 39080724›Full record

ArticleArthritis research & therapy2024

IL-40 is up-regulated in the synovial fluid and cartilage of osteoarthritis patients and contributes to the alteration of chondrocytes phenotype in vitro.

L Andrés Cerezo, A Navrátilová, M Kuklová, A Prokopcová, J Baloun, T Kropáčková, D Veigl, S Popelka, P Fulín, R Ballay and 3 more

Abstract read
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Article in Arthritis research & therapy, 2024. 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
–field-weighted citation impact
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.

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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

13 authors.

L Andrés CerezoInstitute of Rheumatology, Na Slupi 4, 128 50, Prague, Czech Republic.
A NavrátilováInstitute of Rheumatology, Na Slupi 4, 128 50, Prague, Czech Republic.
M KuklováInstitute of Rheumatology, Na Slupi 4, 128 50, Prague, Czech Republic.
A ProkopcováInstitute of Rheumatology, Na Slupi 4, 128 50, Prague, Czech Republic.
J BalounInstitute of Rheumatology, Na Slupi 4, 128 50, Prague, Czech Republic.
T KropáčkováInstitute of Rheumatology, Na Slupi 4, 128 50, Prague, Czech Republic.
D VeiglInstitute of Rheumatology, Na Slupi 4, 128 50, Prague, Czech Republic.
S PopelkaInstitute of Rheumatology, Na Slupi 4, 128 50, Prague, Czech Republic.
P FulínDepartment of Rheumatology, 1st Faculty of Medicine, Charles University, Prague, Czech Republic.
R BallayDepartment of Rheumatology, 1st Faculty of Medicine, Charles University, Prague, Czech Republic.
K PavelkaInstitute of Rheumatology, Na Slupi 4, 128 50, Prague, Czech Republic.
J VencovskýInstitute of Rheumatology, Na Slupi 4, 128 50, Prague, Czech Republic.
L ŠenoltInstitute of Rheumatology, Na Slupi 4, 128 50, Prague, Czech Republic. senolt@revma.cz.

Funding

Ministerstvo Zdravotnictví Ceské Republiky NU21-05-00276Ministerstvo Zdravotnictví Ceské Republiky RVO 00023728Ministry of Education Youth and Sports of the Czech Republic SVV 260523
6 · The paper itself

Abstract

introductionIL-40 is a novel cytokine associated with autoimmune connective tissue disorders such as rheumatoid arthritis (RA) or Sjögren syndrome. We have previously shown an accumulation of IL-40 in the RA joint and its expression by immune cells and fibroblasts. Therefore, we aimed to assess the role of IL-40 in association with hyaline cartilage and chondrocyte activity.

methodsImmunohistochemistry was employed to detect IL-40 in paired samples of loaded and unloaded regions of osteoarthritis (OA) cartilage (n=5). Synovial fluid IL-40 was analysed by ELISA in OA (n=31) and control individuals after knee injury (n=34). The impact of IL-40 on chondrocytes was tested in vitro.

resultsIL-40 was found in chondrocytes of the superficial zone of the OA cartilage, both in loaded and unloaded explants. Additionally, only biopsies from loaded explants showed significant IL-40 positivity in transitional zone chondrocytes. Levels of IL-40 were significantly elevated in the synovial fluid from OA patients compared to controls (p<0.0009) and correlated with synovial fluid leukocyte counts in OA (r=0.444, p=0.014). Chondrocytes exposed to IL-40 dose dependently increased in the secretion of pro-inflammatory cytokines IL-6 (p<0.0001) and IL-8 (p=0.004). Moreover, a dose dependent up-regulation of matrix degrading metalloproteinases MMP-1 (p=0.004), MMP-3 (p=0.031) and MMP-13 (p=0.0002) upon IL-40 treatment was observed in contrast to untreated chondrocytes.

conclusionThis study is the first to demonstrate the accumulation of IL-40 in OA cartilage and its up-regulation in the synovial fluid of OA patients compared to controls. In addition, extracellular IL-40 appears to play a role in promoting inflammation and cartilage destruction by driving chondrocyte behaviour towards a more aggressive phenotype.

Indexed as

ChondrocytesInterleukinsOsteoarthritisSynovial FluidAdultAgedCartilage, ArticularCells, CulturedEnzyme-Linked Immunosorbent AssayFemaleHumansImmunohistochemistryMaleMiddle AgedPhenotypeUp-RegulationC17orf99 protein, humanInterleukinsCartilageChondrocytesInterleukin 40Osteoarthritis

Identifiers

PMID39080724
PMCPMC11289996

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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.