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Animals : an open access journal from MDPI2026; 16(10); 1523; doi: 10.3390/ani16101523

Clinical Outcomes Following Intra-Articular Administration of Autologous Muscle-Derived Mesenchymal Stem Cells in Horses with Chronic Osteoarthritis: A Prospective Open-Label Study.

Abstract: Mesenchymal stromal/stem cells (MSCs) are increasingly investigated as intra-articular therapies for equine osteoarthritis (OA), although most studies have focused on allogeneic or combination-based approaches. Evidence supporting the use of autologous MSCs as a stand-alone treatment remains limited. The present study evaluated the safety and clinical evolution following intra-articular administration of autologous muscle-derived MSCs (mdMSCs) in horses with naturally occurring chronic OA. Thirteen horses with confirmed clinical disease were included. Each affected joint received a single injection, with the administered cell dose adapted to joint size (1 × 10 or 2 × 10 cells). Clinical assessments were conducted at baseline and at 6 and 12 weeks post-treatment using the American Association of Equine Practitioners (AAEP) lameness scale, together with a joint inflammation score and a composite total clinical score (TCS). Clinical scores decreased over time, with statistically significant improvements observed at both follow-up time points. Seven of thirteen horses met the predefined responder criteria based on AAEP improvement, including complete resolution of lameness in several cases. The treatment was well tolerated, with only mild and transient local reactions that resolved without intervention. These results indicate that intra-articular administration of autologous mdMSCs is associated with clinically relevant improvement in horses with chronic OA.
Publication Date: 2026-05-15 PubMed ID: 42193813DOI: 10.3390/ani16101523Google Scholar: Lookup
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  • Journal Article

Summary

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Overview

Background

  • Osteoarthritis (OA) is a common joint disease in horses causing pain, inflammation, and lameness.
  • Mesenchymal stem/stromal cells (MSCs) have regenerative and anti-inflammatory properties, making them a potential therapeutic approach for OA.
  • Most prior research has focused on allogeneic (donor-derived) MSCs or treatments combining MSCs with other agents.
  • There is limited evidence on using autologous (self-derived) MSCs alone, particularly those derived from muscle tissue (mdMSCs), for equine OA treatment.

Study Design

  • This was a prospective open-label clinical study involving 13 horses diagnosed with naturally occurring chronic OA.
  • Each horse received a single intra-articular injection of autologous mdMSCs into the affected joint.
  • The cell dose was scaled to the joint size: either 1 × 10^6 or 2 × 10^6 cells per joint.
  • Assessments were made at baseline (pre-treatment), 6 weeks post-treatment, and 12 weeks post-treatment.

Outcome Measures

  • Lameness was evaluated using the standard American Association of Equine Practitioners (AAEP) lameness scale, which grades severity.
  • Joint inflammation was scored to monitor any potential inflammatory reactions in response to the treatment.
  • A composite total clinical score (TCS) combined lameness and inflammation assessments to provide an overall clinical picture.
  • Responder criteria were predefined, likely including thresholds of improvement in lameness scores.

Results

  • Clinical scores showed a significant decrease (improvement) at both 6 and 12 weeks compared to baseline.
  • Seven out of thirteen horses met the responder criteria, with some achieving complete resolution of lameness.
  • The treatment was well tolerated with no serious adverse effects reported.
  • Only mild, temporary local reactions (e.g., minor inflammation) were observed and resolved without needing any medical intervention.

Conclusions

  • Intra-articular injection of autologous muscle-derived MSCs appears to be a safe and effective stand-alone treatment option for chronic osteoarthritis in horses.
  • This suggests an encouraging alternative to allogeneic or combination therapies, potentially minimizing risks of immune reactions or complications.
  • These promising results warrant further investigation through larger controlled studies to confirm benefits and optimize treatment protocols.

Cite This Article

APA
Serteyn D, Graide H, Ceusters J, Vandersmissen M, Salciccia A, Sandersen C, Lejeune JP. (2026). Clinical Outcomes Following Intra-Articular Administration of Autologous Muscle-Derived Mesenchymal Stem Cells in Horses with Chronic Osteoarthritis: A Prospective Open-Label Study. Animals (Basel), 16(10), 1523. https://doi.org/10.3390/ani16101523

Publication

ISSN: 2076-2615
NlmUniqueID: 101635614
Country: Switzerland
Language: English
Volume: 16
Issue: 10
PII: 1523

Researcher Affiliations

Serteyn, Didier
  • Center for Oxygen Research and Development, Fundamental and Applied Research for Animals and Health, University of Liege, 4000 Liege, Belgium.
  • Equine Research Center, 6698 Vielsalm, Belgium.
  • Revatis S.A., 6900 Marche-En-Famenne, Belgium.
Graide, Hélène
  • Center for Oxygen Research and Development, Fundamental and Applied Research for Animals and Health, University of Liege, 4000 Liege, Belgium.
  • Revatis S.A., 6900 Marche-En-Famenne, Belgium.
Ceusters, Justine
  • Center for Oxygen Research and Development, Fundamental and Applied Research for Animals and Health, University of Liege, 4000 Liege, Belgium.
  • Revatis S.A., 6900 Marche-En-Famenne, Belgium.
Vandersmissen, Maxime
  • Equine Clinic, Faculty of Veterinary Medicine, University of Liege, 4000 Liege, Belgium.
Salciccia, Alexandra
  • Equine Clinic, Faculty of Veterinary Medicine, University of Liege, 4000 Liege, Belgium.
Sandersen, Charlotte
  • Center for Oxygen Research and Development, Fundamental and Applied Research for Animals and Health, University of Liege, 4000 Liege, Belgium.
  • Equine Research Center, 6698 Vielsalm, Belgium.
  • Equine Clinic, Faculty of Veterinary Medicine, University of Liege, 4000 Liege, Belgium.
Lejeune, Jean-Philippe
  • Equine Research Center, 6698 Vielsalm, Belgium.

Grant Funding

  • 000736 / Revatis SA

Citations

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