Evidence map›Paper›PMID 41303430›Full record

ReviewInternational journal of molecular sciences2025

Inflaming and Immune-Resolving: The Ambivalent Role of Eosinophils in Osteoarthritis.

Silvia Costantini, Paolo Dolzani, Veronica Panichi, Rosa Maria Borzì, Paulraj Balaji, Maria Daglia, Carla Renata Arciola

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

7 authors.

Silvia CostantiniDepartment of Medical and Surgical Sciences (DIMEC), Alma Mater Studiorum University of Bologna, 40136 Bologna, Italy.
Paolo DolzaniLaboratory of Immunorheumatology and Tissue Regeneration, IRCCS Istituto Ortopedico Rizzoli, 40136 Bologna, Italy.ORCID 0000-0002-9341-2703
Veronica PanichiLaboratory of Immunorheumatology and Tissue Regeneration, IRCCS Istituto Ortopedico Rizzoli, 40136 Bologna, Italy.ORCID 0000-0001-6236-182X
Rosa Maria BorzìLaboratory of Immunorheumatology and Tissue Regeneration, IRCCS Istituto Ortopedico Rizzoli, 40136 Bologna, Italy.ORCID 0000-0003-4133-4894
Paulraj BalajiPG and Research Centre in Biotechnology, MGR College, Hosur 635130, TN, India.ORCID 0000-0002-6839-4785
Maria DagliaDepartment of Pharmacy, University of Naples Federico II, Via D. Montesano 49, 80131 Naples, Italy.ORCID 0000-0002-4870-7713
Carla Renata ArciolaDepartment of Medical and Surgical Sciences (DIMEC), Alma Mater Studiorum University of Bologna, 40136 Bologna, Italy.ORCID 0000-0003-0382-0066

Funding

5x1000 2021 Project "Chronic inflammation and cellular senescence: characterization of the senescent phenotype of chondrocytes and synoviocytes of patients suffering from osteoarthritis and rheumatoid arthritis and effects of the septic milieu" (n. 2023/7 2023/730961, CUP D33C22001720001.
6 · The paper itself

Abstract

Osteoarthritis (OA), the most prevalent form of arthropathy, is characterized by progressive degradation of cartilage, synovial inflammation, and other pathological changes that gradually affect the entire joint. Once regarded as a purely degenerative disease with minimal immune involvement, recent evidence reveals that chronic low-grade inflammation, insidiously fueled by the destructive crosstalk between cartilage and synovium, plays a key role in OA pathophysiology. Among the immune cells involved, eosinophils have emerged as unexpected yet significant contributors, exhibiting both pro-inflammatory and immunoregulatory properties. Traditionally associated with allergic responses and antiparasitic defense, eosinophils can also secrete anti-inflammatory cytokines along with specialized pro-resolving lipid mediators (SPMs) that promote macrophage polarization toward reparative M2 phenotypes. Eosinophils may sustain inflammation or, conversely, act as "silent modulators" that subtly shape the immune microenvironment and support tissue homeostasis. This immunological plasticity positions them at the intersection of joint damage and repair. This article explores emerging evidence on eosinophil activity in OA, emphasizing their dual nature and potential as therapeutic targets to shift the joint

Indexed as

EosinophilsOsteoarthritisAnimalsCytokinesHumansInflammationMacrophagesCytokinescartilage degradationcytokines (IL-10eosinophilsimmune modulationjoint preservationlow-grade inflammationosteoarthritisspecialized pro-resolving mediators (SPMs)synovial inflammationTGF-β)therapeutic targets in osteoarthritis

Identifiers

PMID41303430
PMCPMC12652785

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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.