Evidence map›Paper›PMID 25889681›Full record

ArticleStem cell research & therapy2015

Development of a simple procedure for the treatment of femoral head osteonecrosis with intra-osseous injection of bone marrow mesenchymal stromal cells: study of their biodistribution in the early time points after injection.

Angélique Lebouvier, Alexandre Poignard, Madeleine Cavet, Jérôme Amiaud, Julie Leotot, Philippe Hernigou, Alain Rahmouni, Philippe Bierling, Pierre Layrolle, Hélène Rouard and 1 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 3 pooled it
4.8field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 3 syntheses or guidelines pooled it, 50 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

11 authors at 5 institutions in 1 country.

Angélique LebouvierUniversité Paris-Est, Faculté de médecine, Laboratoire de "Bioingénierie cellulaire, tissulaire et sanguine", EA3952, 5 rue Gustave Eiffel, 94000, Créteil, France. angelique.lebouvier@gmail.com.
Alexandre PoignardUniversité Paris-Est, Faculté de médecine, Laboratoire de "Bioingénierie cellulaire, tissulaire et sanguine", EA3952, 5 rue Gustave Eiffel, 94000, Créteil, France. alexandre.poignard@hmn.aphp.fr.
Madeleine CavetService de radiologie Albert Chenevier, AP-HP Hôpital Henri-Mondor, 51 Avenue du Maréchal de Lattre de Tassigny, 94000, Créteil, France. mcavet@gmail.com.
Jérôme AmiaudInserm U957, Laboratory for Pathophysiology of Bone Resorption, Faculty of Medicine, University of Nantes, 1 rue Gaston Veil, 44035, Nantes cedex 1, France. jerome.amiaud@univ-nantes.fr.
Julie LeototUniversité Paris-Est, Faculté de médecine, Laboratoire de "Bioingénierie cellulaire, tissulaire et sanguine", EA3952, 5 rue Gustave Eiffel, 94000, Créteil, France. leotot.julie@orange.fr.
Philippe HernigouUniversité Paris-Est, Faculté de médecine, Laboratoire de "Bioingénierie cellulaire, tissulaire et sanguine", EA3952, 5 rue Gustave Eiffel, 94000, Créteil, France. philippe.hernigou@hmn.aphp.fr.
Alain RahmouniService de radiologie Albert Chenevier, AP-HP Hôpital Henri-Mondor, 51 Avenue du Maréchal de Lattre de Tassigny, 94000, Créteil, France. alain.rahmouni@hmn.aphp.fr.
Philippe BierlingEtablissement Français du Sang d'Ile-de-France, Unité d'Ingénierie et de Thérapie Cellulaire, 5 rue Gustave Eiffel, 94017, Créteil cedex, France. philippe.bierling@efs.sante.fr.
Pierre LayrolleInserm U957, Laboratory for Pathophysiology of Bone Resorption, Faculty of Medicine, University of Nantes, 1 rue Gaston Veil, 44035, Nantes cedex 1, France. pierre.layrolle@inserm.fr.
Hélène RouardUniversité Paris-Est, Faculté de médecine, Laboratoire de "Bioingénierie cellulaire, tissulaire et sanguine", EA3952, 5 rue Gustave Eiffel, 94000, Créteil, France. helene.rouard@efs.sante.fr.
Nathalie ChevallierUniversité Paris-Est, Faculté de médecine, Laboratoire de "Bioingénierie cellulaire, tissulaire et sanguine", EA3952, 5 rue Gustave Eiffel, 94000, Créteil, France. nathalie.chevallier@efs.sante.fr.
Université Gustave Eiffel · FRAssistance Publique – Hôpitaux de Paris · FRNantes Université · FRÉtablissement Français du Sang · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOsteonecrosis of the femoral head (ONFH) is a degenerative disease progressing to a femoral head (FH) collapse. Injection of osteoprogenitor cells like bone marrow mesenchymal stromal cells (BMSCs) into the FH appears to be a good therapeutic treatment. However, safety and efficacy of BMSCs to treat bone defect are the main preclinical data required for clinical application. Efficacy and the lack of risk of cell transformation after amplification of BMSCs have been extensively described. The main objectives of this study were to develop a simple and usable procedure for clinicians and control its feasibility by evaluating the biodistribution of BMSCs after injection into the FH in a large animal model. The impact of this approach was evaluated on one natural pig ONFH.

methodsBMSCs were directly injected in the pig FH, and then the biodistribution of grafted cells was detected by quantitative real-time polymerase chain reaction, cytometry, or a combination of classic histology analysis and in situ hybridization (ISH). BMSC efficacy on bone regeneration was evaluated by magnetic resonance imaging (MRI) and histology.

resultsAfter 30-minute and 24-hour follow-up, grafted cells were detected at the injection site and no BMSCs were detected in filter organs or body fluids. The combination of classic histology analysis and ISH showed a good homogeneity of cell distribution in FH. Local delivery of BMSCs onto a bone scaffold associated with bone formation in vivo confirmed the preferential tropism of BMSCs to the bone tissue as well as their efficacy to form bone. Treatment of a natural pig ONFH by autologous BMSCs indicated a beginning of bone healing as early as 2 weeks with a complete healing after 9 weeks. At this stage, MRI and histological analysis were similar to those of a normal FH.

conclusionsIntra-osseous injection of BMSCs in FH seems to be a good strategy for ONFH treatment as the safety concerning the biodistribution of BMSCs is ensured. Moreover, the efficacy of BMSCs in natural ONFH seems to indicate that this is a promising approach. Altogether, these results constitute the preclinical data necessary for the setup of a clinical application with expanded BMSCs in the context of advanced therapy medicinal products.

Indexed as

Mesenchymal Stem Cell TransplantationAnimalsBone and BonesBone Marrow CellsFemaleFemur HeadFemur Head NecrosisHumansInfusions, IntraosseousMaleMesenchymal Stem CellsMiceMice, SCIDOsteogenesisRadiographyReal-Time Polymerase Chain ReactionRibonuclease P

Identifiers

PMID25889681
PMCPMC4448288
OpenAlexW2160094808

What OpenQuestion holds

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LicenceCC BY
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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.