Integrin α10β1-Selected Mesenchymal Stem Cells Reduce Pain and Cartilage Degradation and Increase Immunomodulation in an Equine Osteoarthritis Model

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Objective: Integrin α10β1-selected mesenchymal stem cells (integrin α10-MSCs) have previously shown potential in treating cartilage damage and osteoarthritis (OA) in vitro and in animal models in vivo. The aim of this study was to further investigate disease-modifying effects of integrin α10-MSCs. Design: OA was surgically induced in 17 horses. Eighteen days after surgery, horses received 2 × 107 integrin α10-MSCs intra-articularly or were left untreated. Lameness and response to carpal flexion was assessed weekly along with synovial fluid (SF) analysis. On day 52 after treatment, horses were euthanized, and carpi were evaluated by computed tomography (CT), MRI, histology, and for macroscopic pathology and integrin α10-MSCs were traced in the joint tissues. Results: Lameness and response to carpal flexion significantly improved over time following integrin α10-MSC treatment. Treated horses had milder macroscopic cartilage pathology and lower cartilage histology scores than the untreated group. Prostaglandin E2 and interleukin-10 increased in the SF after integrin α10-MSC injection. Integrin α10-MSCs were found in SF from treated horses up to day 17 after treatment, and in the articular cartilage and subchondral bone from 5 of 8 treated horses after euthanasia at 52 days after treatment. The integrin α10-MSC injection did not cause joint flare. Conclusion: This study demonstrates that intra-articular (IA) injection of integrin α10-MSCs appears to be safe, alleviate pathological changes in the joint, and improve joint function in an equine post-traumatic osteoarthritis (PTOA) model. The results suggest that integrin α10-MSCs hold promise as a disease-modifying osteoarthritis drug (DMOAD).

OriginalsprogEngelsk
TidsskriftCartilage
ISSN1947-6035
DOI
StatusE-pub ahead of print - 2024

Bibliografisk note

Funding Information:
The authors would like to acknowledge Lene Theil Skovgaard for her help with all statistical analyses. The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This study was funded by Xintela AB, Torben og Alice Frimodt Foundation, the Frimodt Heineke Foundation, Direktør Emil C. Hertz og Hustru Inger Hertz’ Foundation, and Direktør Michael Hermann Nielsens Mindelegat.

Publisher Copyright:
© The Author(s) 2023.

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