Evidence map›Paper›PMID 31275328›Full record

ReviewFrontiers in immunology2019

Immune Function and Diversity of Osteoclasts in Normal and Pathological Conditions.

Maria-Bernadette Madel, Lidia Ibáñez, Abdelilah Wakkach, Teun J de Vries, Anna Teti, Florence Apparailly, Claudine Blin-Wakkach

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 129 papers.

0numbers the graph read from it
0cells of the map it votes in
129citing papers in PubMed
9.0field-weighted citation impact, top 1% 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

129 citing papers in PubMed, 197 citations in OpenAlex.

  1. Article
  2. Exacerbation of inflammatory bone loss in TET2-driven clonal hematopoiesis.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Article
  3. Repeated social defeat causes bone loss from mouse femur.Brain, behavior, & immunity - health · 2026
    Article
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  7. Developmental Pathways of Immature CD11cInternational journal of molecular sciences · 2026
    Review
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69 more citing papers are in PubMed but not listed here.

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 at 7 institutions in 4 countries.

Maria-Bernadette MadelCNRS, Laboratoire de PhysioMédecine Moléculaire, Faculté de Médecine, UMR7370, Nice, France.
Lidia IbáñezDepartment of Pharmacy, Cardenal Herrera-CEU University, València, Spain.
Abdelilah WakkachCNRS, Laboratoire de PhysioMédecine Moléculaire, Faculté de Médecine, UMR7370, Nice, France.
Teun J de VriesDepartment of Periodontology, Academic Centre of Dentistry Amsterdam, University of Amsterdam and Vrije Univeristeit, Amsterdam, Netherlands.
Anna TetiDepartment of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
Florence ApparaillyIRMB, INSERM, CHU Montpellier, Université Montpellier, Montpellier, France.
Claudine Blin-WakkachCNRS, Laboratoire de PhysioMédecine Moléculaire, Faculté de Médecine, UMR7370, Nice, France.
Centre National de la Recherche Scientifique · FRLaboratoire de PhysioMédecine Moléculaire · FRUniversidad Cardenal Herrera CEU · ESUniversité Côte d'Azur · FRUniversité de Montpellier · FRUniversity of Amsterdam · NLUniversity of L'Aquila · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoclasts (OCLs) are key players in controlling bone remodeling. Modifications in their differentiation or bone resorbing activity are associated with a number of pathologies ranging from osteopetrosis to osteoporosis, chronic inflammation and cancer, that are all characterized by immunological alterations. Therefore, the 2000s were marked by the emergence of osteoimmunology and by a growing number of studies focused on the control of OCL differentiation and function by the immune system. At the same time, it was discovered that OCLs are much more than bone resorbing cells. As monocytic lineage-derived cells, they belong to a family of cells that displays a wide heterogeneity and plasticity and that is involved in phagocytosis and innate immune responses. However, while OCLs have been extensively studied for their bone resorption capacity, their implication as immune cells was neglected for a long time. In recent years, new evidence pointed out that OCLs play important roles in the modulation of immune responses toward immune suppression or inflammation. They unlocked their capacity to modulate T cell activation, to efficiently process and present antigens as well as their ability to activate T cell responses in an antigen-dependent manner. Moreover, similar to other monocytic lineage cells such as macrophages, monocytes and dendritic cells, OCLs display a phenotypic and functional plasticity participating to their anti-inflammatory or pro-inflammatory effect depending on their cell origin and environment. This review will address this novel vision of the OCL, not only as a phagocyte specialized in bone resorption, but also as innate immune cell participating in the control of immune responses.

Indexed as

Disease SusceptibilityImmunomodulationAnimalsAntigen PresentationBiomarkersBone RemodelingBone ResorptionCell DifferentiationDendritic CellsHumansLymphocyte ActivationMacrophagesMonocytesOsteoclastsPhenotypeBiomarkersdendritic cellimmune modulationinflammationmonocyte heterogeneityosteoclastosteoimmunology

Identifiers

PMID31275328
PMCPMC6594198
OpenAlexW2950364945

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.