Cell Therapy Department, Hôpital de la Conception, AP-HM, INSERM CIC BT 1409, 13005 Marseille, France.
Aix Marseille University, INSERM, INRAE, C2VN, 13005 Marseille, France.
Cells. 2020 Sep 24;9(10):2158. doi: 10.3390/cells9102158.
The therapeutic use of adipose-derived stromal vascular fraction (SVF) is expanding in multiple pathologies. Various processes have been proposed for manufacturing SVF but they must be revisited based on advanced therapy medicinal product (ATMP) regulations. We report here the development and validation of a fully good manufacturing practices (GMP)-compliant protocol for the isolation of SVF. Adipose tissue was collected from healthy volunteers undergoing lipoaspiration. The optimal conditions of collagenase digestion and washing were determined based on measurements of SVF cell viability, yield recovery, and cell subset distribution. Comparability of the SVF obtained using the newly developed manufacturing process (n = 6) and the Celution-based automated method (n = 33), used as a reference, was established using inter-donor analyses. Characteristics of SVF (n = 5) generated using both manufacturing protocols were analyzed for an intra-donor comparison. In addition, these comparisons also included the determination of colony-forming unit fibroblast frequency, in vitro angiogenic activity, and in vivo regenerative effects in a mouse ischemic cutaneous wound model. We successfully developed a process for the generation of SVF presenting higher cell viability and yield recovery compared to the Celution device-based protocol. Characteristics of the SVF including phenotype, capacity for angiogenesis, and wound-healing promotion attested to the comparability of the two manufacturing processes. We validated an optimized non-automated process that should allow for a GMP-compliant, more affordable, and reduced-cost strategy to exploit the potential of SVF-based regenerative therapies.
脂肪来源的基质血管部分(SVF)的治疗用途正在多种疾病中不断扩展。已经提出了多种用于制造 SVF 的方法,但根据先进治疗药物(ATMP)法规,这些方法必须重新审视。我们在此报告了一种完全符合良好生产规范(GMP)的 SVF 分离协议的开发和验证。从接受吸脂术的健康志愿者中收集脂肪组织。根据 SVF 细胞活力、产率回收和细胞亚群分布的测量,确定了胶原酶消化和洗涤的最佳条件。使用新开发的制造工艺(n = 6)和 Celution 自动化方法(n = 33)获得的 SVF 的可比性,通过供体间分析得到了确立,Celution 自动化方法用作参考。使用两种制造方案生成的 SVF(n = 5)的特征进行了供体间比较。此外,这些比较还包括在小鼠缺血性皮肤创面模型中测定成纤维细胞集落形成单位频率、体外血管生成活性和体内再生效果。我们成功开发了一种 SVF 生成工艺,与基于 Celution 设备的方案相比,该工艺具有更高的细胞活力和产率回收。SVF 的特征,包括表型、血管生成能力和促进伤口愈合的能力,证明了两种制造工艺的可比性。我们验证了一种优化的非自动化工艺,该工艺应允许符合 GMP 的、更经济实惠的、降低成本的策略来利用基于 SVF 的再生疗法的潜力。