Intra-articular injection of two different doses of autologous bone marrow mesenchymal stem cells versus hyaluronic acid in the treatment of knee osteoarthritis: multicenter randomized controlled clinical trial (phase I/II)

Mesenchymal stromal cells are a promising option to treat knee osteoarthritis. Their safety and usefulness must be confirmed and the optimal dose established. We tested increasing doses of bone marrow mesenchymal stromal cells (BM-MSCs) in combination with hyaluronic acid in a randomized clinical tr...

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Veröffentlicht in:Journal of translational medicine 2016-08, Vol.14 (1), p.246-246, Article 246
Hauptverfasser: Lamo-Espinosa, José M, Mora, Gonzalo, Blanco, Juan F, Granero-Moltó, Froilán, Nuñez-Córdoba, Jorge M, Sánchez-Echenique, Carmen, Bondía, José M, Aquerreta, Jesús Dámaso, Andreu, Enrique J, Ornilla, Enrique, Villarón, Eva M, Valentí-Azcárate, Andrés, Sánchez-Guijo, Fermín, Del Cañizo, María Consuelo, Valentí-Nin, Juan Ramón, Prósper, Felipe
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Sprache:eng
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Zusammenfassung:Mesenchymal stromal cells are a promising option to treat knee osteoarthritis. Their safety and usefulness must be confirmed and the optimal dose established. We tested increasing doses of bone marrow mesenchymal stromal cells (BM-MSCs) in combination with hyaluronic acid in a randomized clinical trial. A phase I/II multicenter randomized clinical trial with active control was conducted. Thirty patients diagnosed with knee OA were randomly assigned to intraarticularly administered hyaluronic acid alone (control), or together with 10 × 10(6) or 100 × 10(6) cultured autologous BM-MSCs, and followed up for 12 months. Pain and function were assessed using VAS and WOMAC and by measuring the knee motion range. X-ray and magnetic resonance imaging analyses were performed to analyze joint damage. No adverse effects were reported after BM-MSC administration or during follow-up. BM-MSC-administered patients improved according to VAS during all follow-up evaluations and median value (IQR) for control, low-dose and high-dose groups change from 5 (3, 7), 7 (5, 8) and 6 (4, 8) to 4 (3, 5), 2 (1, 3) and 2 (0,4) respectively at 12 months (low-dose vs control group p = 0.005 and high-dose vs control group p 
ISSN:1479-5876
1479-5876
DOI:10.1186/s12967-016-0998-2