Evidence map›Paper›PMID 34925336›Full record

ArticleFrontiers in immunology2021

Preventive CCL2/CCR2 Axis Blockade Suppresses Osteoclast Activity in a Mouse Model of Rheumatoid Arthritis by Reducing Homing of CCR2

Darja Flegar, Maša Filipović, Alan Šućur, Antonio Markotić, Nina Lukač, Dino Šisl, Marina Ikić Matijašević, Zrinka Jajić, Tomislav Kelava, Vedran Katavić and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

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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

12 authors at 3 institutions in 2 countries.

Darja FlegarDepartment of Physiology and Immunology, University of Zagreb School of Medicine, Zagreb, Croatia.
Maša FilipovićDepartment of Physiology and Immunology, University of Zagreb School of Medicine, Zagreb, Croatia.
Alan ŠućurDepartment of Physiology and Immunology, University of Zagreb School of Medicine, Zagreb, Croatia.
Antonio MarkotićCenter for Clinical Pharmacology, University Clinical Hospital Mostar, Mostar, Bosnia and Herzegovina.
Nina LukačLaboratory for Molecular Immunology, Croatian Institute for Brain Research, University of Zagreb School of Medicine, Zagreb, Croatia.
Dino ŠislDepartment of Physiology and Immunology, University of Zagreb School of Medicine, Zagreb, Croatia.
Marina Ikić MatijaševićDepartment of Clinical Immunology, Rheumatology and Pulmology, Sveti Duh University Hospital, Zagreb, Croatia.
Zrinka JajićDepartment of Rheumatology, Physical Medicine and Rehabilitation, Clinical Hospital Center Sestre Milosrdnice, University of Zagreb School of Medicine, Zagreb, Croatia.
Tomislav KelavaDepartment of Physiology and Immunology, University of Zagreb School of Medicine, Zagreb, Croatia.
Vedran KatavićLaboratory for Molecular Immunology, Croatian Institute for Brain Research, University of Zagreb School of Medicine, Zagreb, Croatia.
Nataša KovačićLaboratory for Molecular Immunology, Croatian Institute for Brain Research, University of Zagreb School of Medicine, Zagreb, Croatia.
Danka GrčevićDepartment of Physiology and Immunology, University of Zagreb School of Medicine, Zagreb, Croatia.
University of Zagreb · HRKlinička bolnica "Sveti Duh" · HRUniversity of Mostar · BA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Detailed characterization of medullary and extramedullary reservoirs of osteoclast progenitors (OCPs) is required to understand the pathophysiology of increased periarticular and systemic bone resorption in arthritis. In this study, we focused on identifying the OCP population specifically induced by arthritis and the role of circulatory OCPs in inflammatory bone loss. In addition, we determined the relevant chemokine axis responsible for their migration, and targeted the attraction signal to reduce bone resorption in murine collagen-induced arthritis (CIA). OCPs were expanded in periarticular as well as circulatory compartment of arthritic mice, particularly the CCR2

Indexed as

AnimalsAntirheumatic AgentsArthritis, ExperimentalArthritis, RheumatoidBenzoxazinesBone and BonesCell DifferentiationCell MovementCells, CulturedChemokine CCL2Disease Models, AnimalFlow CytometryHumansMaleMesenchymal Stem CellsMethotrexateAntirheumatic AgentsBenzoxazinesChemokine CCL2MethotrexateReceptors, CCR2RS 504393Spiro Compoundschemokineshuman arthritisinflammationmouse arthritismyeloid cellsosteoclasts

Identifiers

PMID34925336
PMCPMC8677701
OpenAlexW4200221799

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.