Andersen Camilla, Jacobsen Stine, Uvebrant Kristina, Griffin John F, Vonk Lucienne Angela, Walters Marie, Berg Lise Charlotte, Lundgren-Åkerlund Evy, Lindegaard Casper
Department of Veterinary Clinical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Taastrup, Denmark.
Xintela AB, Lund, Sweden.
Cartilage. 2025 Jun;16(2):250-264. doi: 10.1177/19476035231209402. Epub 2023 Nov 21.
ObjectiveIntegrin α10β1-selected mesenchymal stem cells (integrin α10-MSCs) have previously shown potential in treating cartilage damage and osteoarthritis (OA) and in animal models . The aim of this study was to further investigate disease-modifying effects of integrin α10-MSCs.DesignOA was surgically induced in 17 horses. Eighteen days after surgery, horses received 2 × 10 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.ResultsLameness 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.ConclusionThis 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).
整合素α10β1选择的间充质干细胞(整合素α10间充质干细胞)先前已在动物模型中显示出治疗软骨损伤和骨关节炎(OA)的潜力。本研究的目的是进一步研究整合素α10间充质干细胞的疾病修饰作用。
对17匹马进行手术诱导骨关节炎。术后18天,马匹接受关节内注射2×10个整合素α10间充质干细胞或不进行治疗。每周评估跛行情况和对腕关节屈曲的反应,并进行滑液(SF)分析。治疗后第52天,对马匹实施安乐死,通过计算机断层扫描(CT)、磁共振成像(MRI)、组织学检查评估腕关节,并检查宏观病理学情况,同时在关节组织中追踪整合素α10间充质干细胞。
整合素α10间充质干细胞治疗后,跛行情况和对腕关节屈曲的反应随时间显著改善。与未治疗组相比,治疗后的马匹宏观软骨病理学表现较轻,软骨组织学评分较低。整合素α10间充质干细胞注射后,滑液中的前列腺素E2和白细胞介素-10增加。在治疗后第17天之前,在治疗马匹的滑液中发现了整合素α10间充质干细胞,在治疗后52天实施安乐死时,在8匹治疗马匹中的5匹马的关节软骨和软骨下骨中发现了整合素α10间充质干细胞。整合素α10间充质干细胞注射未引起关节炎症。
本研究表明,在马创伤后骨关节炎(PTOA)模型中,关节内(IA)注射整合素α10间充质干细胞似乎是安全的,可减轻关节的病理变化并改善关节功能。结果表明,整合素α10间充质干细胞有望成为一种疾病修饰性骨关节炎药物(DMOAD)。