Gradalis, Inc, Dallas, TX, 75006, USA.
University of Michigan Biointerfaces Institute, Ann Arbor, MI, 48109, USA.
Sci Rep. 2024 Jul 5;14(1):15556. doi: 10.1038/s41598-024-65993-3.
Previously, we reported successful cellular expansion of a murine colorectal carcinoma cell line (CT-26) using a three-dimensional (3D) engineered extracellular matrix (EECM) fibrillar scaffold structure. CCL-247 were grown over a limited time period of 8 days on 3D EECM or tissue culture polystyrene (TCPS). Cells were then assayed for growth, electroporation efficiency and Vigil manufacturing release criteria. Using EECM scaffolds, we report an expansion of CCL-247 (HCT116), a colorectal carcinoma cell line, from a starting concentration of 2.45 × 10 cells to 1.9 × 10 cells per scaffold. Following expansion, 3D EECM-derived cells were assessed based on clinical release criteria of the Vigil manufacturing process utilized for Phase IIb trial operation with the FDA. 3D EECM-derived cells passed all Vigil manufacturing release criteria including cytokine expression. Here, we demonstrate successful Vigil product manufacture achieving the specifications necessary for the clinical trial product release of Vigil treatment. Our results confirm that 3D EECM can be utilized for the expansion of human cancer cell CCL-247, justifying further clinical development involving human tissue sample manufacturing including core needle biopsy and minimal ascites samples.
此前,我们报告了使用三维(3D)工程细胞外基质(EECM)纤维支架结构成功地对小鼠结直肠癌细胞系(CT-26)进行细胞扩增。CCL-247 在 3D EECM 或组织培养聚苯乙烯(TCPS)上培养 8 天的有限时间内生长。然后对细胞进行生长、电穿孔效率和 Vigil 制造释放标准的检测。使用 EECM 支架,我们报告了结肠直肠癌细胞系 CCL-247(HCT116)的扩增,从起始浓度 2.45×10 个细胞增加到每个支架 1.9×10 个细胞。扩增后,根据用于 FDA 二期试验操作的 Vigil 制造过程的临床释放标准评估 3D EECM 衍生细胞。3D EECM 衍生细胞通过了所有 Vigil 制造释放标准,包括细胞因子表达。在这里,我们成功地制造了 Vigil 产品,达到了临床试验产品释放的规格要求。我们的结果证实,3D EECM 可用于人类癌症细胞 CCL-247 的扩增,为进一步涉及人体组织样本制造的临床开发提供了依据,包括核心针活检和最小量腹水样本。