Cabrera-Pérez Raquel, Carreras-Sánchez Irene, Roig-Molina Ángela, López-Fernández Alba, Portas-Torres Irene, Batlle-Morera Laura, Vélez Roberto, Vives Joaquim
Bioprocessing for Advanced Cell Therapies (BACT) Group, Cell Therapy Service, Blood and Tissue Bank (BST), 08005 Barcelona, Catalonia, Spain.
Musculoskeletal Tissue Engineering Group, Vall d'Hebron Research Institute (VHIR) and Universitat Autònoma de Barcelona (UAB), 08035 Barcelona, Catalonia, Spain.
Cells. 2025 Jun 7;14(12):862. doi: 10.3390/cells14120862.
Secondary osteonecrosis (ON) is a common complication in paediatric cancer survivors. Combining multipotent mesenchymal stromal cells (MSCs) with core decompression surgery halts disease progression and stimulates bone regeneration. However, the success of advanced therapy medicinal products (ATMPs) requires versatile "off-the-shelf" tissue engineering products (TEPs). This study evaluated the safety and efficacy of TEPs loaded with allogeneic MSCs from Wharton's jelly (WJ-MSCs) in a large-animal model of bone regeneration to support a paediatric investigational plan for ON patients. WJ-MSC-laden fibrin-based hydrogels combined with a synthetic bone substitute (PRO-DENSE) were tested in 16 juvenile sheep (8 males and 8 females) distributed in four experimental groups. Each animal received four cylindrical bone defects in the femoral and tibial epiphyses and was assessed at 6 and 12 weeks. Safety was confirmed, and bone regeneration was observed across all groups. A combination of WJ-MSCs with PRO-DENSE led to improved histological scores, osteogenesis, and construct integration. Trabecular bone volume also increased more in cellular groups over time. However, effects were inconsistent across groups, reflecting the variability seen in clinical trials and highlighting the significant impact of factors such as immunogenetic compatibility, MSC batch potency, and interaction with the recipient's microenvironment on the therapeutic effectiveness and successful clinical translation of allogeneic ATMPs.
继发性骨坏死(ON)是儿童癌症幸存者中的常见并发症。将多能间充质基质细胞(MSCs)与髓芯减压手术相结合可阻止疾病进展并刺激骨再生。然而,先进治疗医药产品(ATMPs)的成功需要通用的“现货供应”组织工程产品(TEPs)。本研究在大型骨再生动物模型中评估了负载来自脐带华通氏胶间充质干细胞(WJ-MSCs)的TEPs的安全性和有效性,以支持针对ON患者的儿科研究计划。将负载WJ-MSCs的纤维蛋白基水凝胶与合成骨替代物(PRO-DENSE)相结合,在分布于四个实验组的16只幼年绵羊(8只雄性和8只雌性)中进行测试。每只动物在股骨和胫骨骨骺处接受四个圆柱形骨缺损,并在6周和12周时进行评估。安全性得到证实,所有组均观察到骨再生。WJ-MSCs与PRO-DENSE的组合导致组织学评分、成骨和植入物整合得到改善。随着时间的推移,细胞组中的小梁骨体积也增加得更多。然而,各实验组之间的效果并不一致,这反映了临床试验中观察到的变异性,并突出了免疫遗传相容性、MSC批次效力以及与受体微环境的相互作用等因素对异体ATMPs治疗效果和成功临床转化的重大影响。