INSERM (French National Institute of Health and Medical Research), UMR 1260, Regenerative Nanomedicine (RNM), FMTS, 11 Rue Humann, 67000, Strasbourg, France.
Université de Strasbourg, Faculté de chirurgie dentaire, Hôpitaux Universitaires de Strasbourg, 8 Rue de Ste Elisabeth, 67000, Strasbourg, France.
Nat Commun. 2019 May 14;10(1):2156. doi: 10.1038/s41467-019-10165-5.
The extended life expectancy and the raise of accidental trauma call for an increase of osteoarticular surgical procedures. Arthroplasty, the main clinical option to treat osteoarticular lesions, has limitations and drawbacks. In this manuscript, we test the preclinical safety of the innovative implant ARTiCAR for the treatment of osteoarticular lesions. Thanks to the combination of two advanced therapy medicinal products, a polymeric nanofibrous bone wound dressing and bone marrow-derived mesenchymal stem cells, the ARTiCAR promotes both subchondral bone and cartilage regeneration. In this work, the ARTiCAR shows 1) the feasibility in treating osteochondral defects in a large animal model, 2) the possibility to monitor non-invasively the healing process and 3) the overall safety in two animal models under GLP preclinical standards. Our data indicate the preclinical safety of ARTiCAR according to the international regulatory guidelines; the ARTiCAR could therefore undergo phase I clinical trial.
预期寿命的延长和意外创伤的增加都需要增加骨关节炎手术。关节置换术是治疗骨关节炎病变的主要临床选择,但存在局限性和缺点。在本手稿中,我们测试了用于治疗骨关节炎病变的创新植入物 ARTiCAR 的临床前安全性。得益于两种先进治疗药物产品的结合,即聚合物纳米纤维骨创面敷料和骨髓间充质干细胞,ARTiCAR 促进了软骨下骨和软骨的再生。在这项工作中,ARTiCAR 显示出 1)在大型动物模型中治疗骨软骨缺损的可行性,2)非侵入性监测愈合过程的可能性,3)在 GLP 临床前标准下的两种动物模型中的整体安全性。我们的数据表明,ARTiCAR 根据国际监管指南具有临床前安全性;因此,ARTiCAR 可以进行 I 期临床试验。