Evidence map›Paper›PMID 35255727›Full record

ArticleCartilage

Folate Receptor Expression by Human Monocyte-Derived Macrophage Subtypes and Effects of Corticosteroids.

Kelly Warmink, Michiel Siebelt, Philip S Low, Frank M Riemers, Bingbing Wang, Saskia G M Plomp, Marianna A Tryfonidou, P René van Weeren, Harrie Weinans, Nicoline M Korthagen

Open access · hybridAbstract read
In one paragraph

Article in Cartilage. 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
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

13 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  4. Article
  5. How Selective are Nanomaterials to Treat Osteoarthritis.International journal of nanomedicine · 2026
    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

10 authors at 4 institutions in 2 countries.

Kelly WarminkDepartment of Orthopedics, University Medical Center Utrecht, Utrecht, The Netherlands.ORCID 0000-0003-4131-675X
Michiel SiebeltDepartment of Orthopedics, Erasmus Medical Center, Rotterdam, The Netherlands.
Philip S LowDepartment of Chemistry, Purdue University, West Lafayette, IN, USA.
Frank M RiemersDepartment of Equine Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.
Bingbing WangDepartment of Chemistry, Purdue University, West Lafayette, IN, USA.
Saskia G M PlompDepartment of Equine Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.
Marianna A TryfonidouDepartment of Equine Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.
P René van WeerenDepartment of Equine Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.
Harrie WeinansDepartment of Orthopedics, University Medical Center Utrecht, Utrecht, The Netherlands.
Nicoline M KorthagenDepartment of Orthopedics, University Medical Center Utrecht, Utrecht, The Netherlands.
Utrecht University · NLPurdue University West Lafayette · USUniversity Medical Center Utrecht · NLErasmus MC · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveFolate receptor beta (FR-β) has been used as a clinical marker and target in multiple inflammatory diseases, including osteoarthritis (OA) and rheumatoid arthritis (RA). However, the conditions under which FR-β

designHuman monocyte-derived macrophages were differentiated to the known M0, M1, or M2 macrophage phenotypes. The phenotype and FR-β expression and plasticity of the macrophage subtypes were determined using flow cytometry, reverse transcription-quantitative polymerase chain reaction (RT-qPCR), and enzyme-linked immunosorbent assay (ELISA).

resultsFR-β expression was low in granulocyte-macrophage colony-stimulating factor (GM-CSF)-generated (M1-like) macrophages and high in macrophage colony-stimulating factor (M-CSF)-generated (M0 and M2-like) macrophages. FR-β expression remained high once the M0 or M2 macrophages were stimulated with pro-inflammatory stimuli (interferon-γ plus lipopolysaccharide) to induce M1-like macrophages. On the contrary, anti-inflammatory TA treatment skewed GM-CSF macrophage differentiation toward an M2 and FR-β

conclusionsAs corticosteroids skewed monocytes toward an FR-β-expressing, anti-inflammatory phenotype, even in an M1 priming GM-CSF environment, FR-β has potential as a biomarker to monitor success of treatment with corticosteroids. Without corticosteroid treatment, M-CSF alone induces high FR-β expression which remains high under pro-inflammatory conditions. This explains why pro-inflammatory FR-β

Indexed as

Adrenal Cortex HormonesFolate Receptor 2Granulocyte-Macrophage Colony-Stimulating FactorMacrophagesBiomarkersFolic AcidHumansMacrophage Colony-Stimulating FactorAdrenal Cortex HormonesBiomarkersFolate Receptor 2Folic AcidFOLR2 protein, humanGranulocyte-Macrophage Colony-Stimulating FactorMacrophage Colony-Stimulating Factorcorticosteroidsdisease markerFR-betaM1/M2macrophages

Identifiers

PMID35255727
PMCPMC9137314
OpenAlexW4220920270

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.