Evidence map›Paper›PMID 40289476›Full record

ArticleThe American journal of sports medicine2025

Allogenic Bioengineered Cartilage Achieves Hyaline Cartilage Repair in a Large Animal Model: A Promising Step Forward.

Halah Kutaish, Laura Bengtsson, Sana Boudabbous, François Lazeyras, Sebastien Courvoisier, Vincent Braunersreuther, Sabine E Hammer, Didier Hannouche, Jacques Ménétrey, Vannary Tieng and 1 more

Abstract read
In one paragraph

Article in The American journal of sports medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Halah KutaishDivision of Orthopaedic Surgery and Traumatology, Department of Surgery, Geneva University Hospitals, Geneva, Switzerland.
Laura BengtssonVanarix, Lausanne, Switzerland.
Sana BoudabbousDivision of Radiology, Diagnostic Department, Geneva University Hospitals, Geneva, Switzerland.
François LazeyrasDivision of Radiology, Diagnostic Department, Geneva University Hospitals, Geneva, Switzerland.
Sebastien CourvoisierDivision of Radiology, Diagnostic Department, Geneva University Hospitals, Geneva, Switzerland.
Vincent BraunersreutherDivision of Clinical Pathology, Diagnostic Department, Geneva University Hospitals, Geneva, Switzerland.
Sabine E HammerInstitute of Immunology, University of Veterinary Medicine Vienna, Vienna, Austria.
Didier HannoucheDivision of Orthopaedic Surgery and Traumatology, Department of Surgery, Geneva University Hospitals, Geneva, Switzerland.
Jacques MénétreyCentre de Médecine du Sport et de L'Exercice, Hirslanden Clinique La Colline, Geneva, Switzerland.
Vannary TiengVanarix, Lausanne, Switzerland.
Philippe M TschollDivision of Orthopaedic Surgery and Traumatology, Department of Surgery, Geneva University Hospitals, Geneva, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChondrocyte-based cell therapy remains a promising method for cartilage repair, despite limitations faced during the last 30 years. PURPOSE/HYPOTHESIS: This work presents hyaline-like bioengineered beads from donor chondrocytes as a novel treatment option for cartilage lesions. It was hypothesized that the implanted cartilage minigrafts would be able to treat cartilage lesions by complete fusion among themselves and by integration with surrounding tissue. No tissue rejection was expected because of cartilage's reported immunological privilege. STUDY

designControlled laboratory study.

methodsAllogenic cartilage beads with hyaline characteristics were produced from frozen chondrocytes of a minipig donor. A total of 8 Göttingen minipigs underwent the implantation of bioengineered cartilage beads into 8 to 10 mm-diameter full-thickness chondral lesions (3 lesions/knee). Animals were sacrificed at 6 weeks (n = 2) and 6 months (n = 6) after implantation. The safety and efficacy of implantation were assessed by macroscopic and histological analyses as well as by magnetic resonance imaging.

resultsNo signs of acute or chronic rejection were observed in any study animals upon implantation. For 6 minipigs at 6 months, magnetic resonance imaging results showed better coverage of the grafted lesions compared with empty (control) lesions. When the cartilage beads were maintained in the lesion, complete integration of the minigrafts with surrounding subchondral bone and native cartilage was observed. Repair tissue in grafted lesions maintained hyaline-like quality and showed evidence of a chondral zonal arrangement at 6 months' follow-up. Additionally, grafted lesions (n = 17) had better macroscopic repair scores than empty lesions (n = 7) (mean inverse Goebel score, 4.24 and 5.57, respectively). Graft-filled lesions showed only a slight superiority in histological repair scores (mean Bern score, 5.76 and 5.43, respectively).

conclusionAllogenic cartilage beads hold potential as an advanced therapy medicinal product for treating cartilage lesions in 1-step surgery with established safety and efficacy. CLINICAL RELEVANCE: This successful preclinical study highlights allogenic cartilage beads as a promising method for cartilage repair. Moreover, using donor chondrocytes may allow reduced patient morbidity and 1-step surgery. Hence, this advanced therapy medicinal product is suitable for treating large lesions and older patients and is currently being evaluated in a phase I/IIa clinical trial.

Indexed as

ChondrocytesHyaline CartilageTissue EngineeringAnimalsDisease Models, AnimalMagnetic Resonance ImagingSwineSwine, MiniatureTransplantation, Homologousallogenic cartilagecartilage imagingcartilage regenerationhyaline cartilagetissue engineering (3D)

Identifiers

PMID40289476
PMCPMC12125493

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.