Nativel Fabien, Smith Audrey, Boulestreau Jeremy, Lépine Charles, Baron Julie, Marquis Melanie, Vignes Caroline, Le Guennec Yoan, Veziers Joelle, Lesoeur Julie, Loll François, Halgand Boris, Renard Denis, Abadie Jerome, Legoff Benoit, Blanchard Frederic, Gauthier Olivier, Vinatier Claire, Rieux Anne des, Guicheux Jerome, Le Visage Catherine
Nantes Université, ONIRIS, Univ Angers, CHU Nantes, INSERM, Regenerative Medicine and Skeleton, RMeS, UMR 1229, F-44000 Nantes, France.
UCLouvain, Louvain Drug Research Institute, Advanced Drug Delivery and Biomaterials, 1200, Bruxelles, Belgium.
Mater Today Bio. 2023 Feb 13;19:100581. doi: 10.1016/j.mtbio.2023.100581. eCollection 2023 Apr.
Osteoarthritis (OA) is an inflammatory joint disease that affects cartilage, subchondral bone, and joint tissues. Undifferentiated Mesenchymal Stromal Cells are a promising therapeutic option for OA due to their ability to release anti-inflammatory, immuno-modulatory, and pro-regenerative factors. They can be embedded in hydrogels to prevent their tissue engraftment and subsequent differentiation. In this study, human adipose stromal cells are successfully encapsulated in alginate microgels via a micromolding method. Microencapsulated cells retain their in vitro metabolic activity and bioactivity and can sense and respond to inflammatory stimuli, including synovial fluids from OA patients. After intra-articular injection in a rabbit model of post-traumatic OA, a single dose of microencapsulated human cells exhibit properties matching those of non-encapsulated cells. At 6 and 12 weeks post-injection, we evidenced a tendency toward a decreased OA severity, an increased expression of aggrecan, and a reduced expression of aggrecanase-generated catabolic neoepitope. Thus, these findings establish the feasibility, safety, and efficacy of injecting cells encapsulated in microgels, opening the door to a long-term follow-up in canine OA patients.
骨关节炎(OA)是一种影响软骨、软骨下骨和关节组织的炎性关节疾病。未分化间充质基质细胞因其能够释放抗炎、免疫调节和促再生因子,是OA一种很有前景的治疗选择。它们可以包埋在水凝胶中以防止其组织植入和随后的分化。在本研究中,人脂肪基质细胞通过微成型方法成功封装在藻酸盐微凝胶中。微囊化细胞保留其体外代谢活性和生物活性,并能感知和响应炎症刺激,包括来自OA患者的滑液。在创伤后OA兔模型中进行关节内注射后,单剂量的微囊化人细胞表现出与未封装细胞相匹配的特性。在注射后6周和12周,我们证明了OA严重程度有降低的趋势、聚集蛋白聚糖表达增加以及聚集蛋白聚糖酶产生的分解代谢新表位表达减少。因此,这些发现证实了注射微凝胶封装细胞的可行性、安全性和有效性,为犬OA患者的长期随访打开了大门。