The Advanced Center for Biochemical Engineering, Universtiy College London, UK.
Biotechnol Prog. 2009 Sep-Oct;25(5):1448-58. doi: 10.1002/btpr.229.
Whole cell therapy is showing potential in the clinic for the treatment of many chronic diseases. The translation of laboratory-scale methods for cell harvesting and formulation to commercial-scale manufacturing offers major bioprocessing challenges. This is especially the case when the cell properties determine the final product effectiveness. This study is focused on developing an ultra scale-down method for assessing the impact of the hydrodynamic environment on human cells that constitute the therapeutic product. Small volumes of a prostate cancer cell line, currently being developed in late phase II clinical trials as an allogeneic whole cell vaccine therapy for prostate cancer, were exposed to hydrodynamic shear rates similar to those present in downstream process, formulation and vial filling operations. A small scale rotating disc shear device (20 mL) was used over a range of disc speeds to expose cells to maximum shear rates ranging from 90 x 10(3) to 175 x 10(3) s(-1) (equivalent maximum power dissipation rates of 14 x 10(3) to 52 x 10(3) W kg(-1)). These cells were subsequently analyzed for critical cell quality attributes such as the retention of membrane integrity and cell surface marker profile and density. Three cell surface markers (CD9, CD147, and HLAA-C) were studied. The cell markers exhibited different levels of susceptibility to hydrodynamic shear but in all cases this was less than or equal to the loss of membrane integrity. It is evident that the marker, or combination or markers, which might provide the required immunogenic response, will be affected by hydrodynamic shear environment during bioprocessing, if the engineering environment is not controlled to within the limits tolerated by the cell components.
整体细胞治疗在治疗许多慢性疾病的临床中显示出潜力。将细胞收获和配方的实验室规模方法转化为商业规模制造,带来了主要的生物加工挑战。当细胞特性决定最终产品的有效性时,尤其如此。本研究专注于开发一种超缩小方法,用于评估对构成治疗产品的人类细胞的流体动力环境的影响。目前正在进行 II 期临床试验后期开发的前列腺癌细胞系的小体积,作为前列腺癌的同种异体全细胞疫苗治疗,暴露于类似于下游工艺、配方和小瓶灌装操作中存在的流体剪切率。使用小型旋转圆盘剪切设备(20 毫升)在一系列圆盘速度下使细胞暴露于最大剪切率范围为 90×10(3)至 175×10(3)s(-1)(等效最大功率耗散率为 14×10(3)至 52×10(3)Wkg(-1))。随后分析这些细胞的关键细胞质量属性,例如膜完整性和细胞表面标志物的保留和密度。研究了三种细胞表面标志物(CD9、CD147 和 HLAA-C)。细胞标志物表现出对流体剪切不同程度的敏感性,但在所有情况下,这都小于或等于膜完整性的丧失。显然,如果工程环境不受细胞成分可耐受的限制控制,那么在生物加工过程中,可能提供所需免疫原性反应的标志物或标志物组合,将受到流体动力剪切环境的影响。