School of Engineering, Newcastle University, Newcastle upon Tyne, NE1 7RU, UK.
Currently, Evox Therapeutics, Medawar Centre, Oxford OX4 4HG, UK.
Biotechnol Adv. 2020 Dec;45:107637. doi: 10.1016/j.biotechadv.2020.107637. Epub 2020 Sep 25.
The emergence of cell gene therapy (CGT) as a safe and efficacious treatment for numerous severe inherited and acquired human diseases has led to growing interest and investment in new CGT products. The most successful of these have been autologous viral vector-based treatments. The development of viral vector manufacturing processes and ex vivo patient cell processing capabilities is a pressing issue in the advancement of autologous viral vector-based CGT treatments. In viral vector production, scale-up is a critical task due to the limited scalability of traditional laboratory systems and the demand for high volumes of viral vector manufactured in accordance with current good manufacturing practice. Ex vivo cell processing methods require optimisation and automation before they can be scaled out, and several other manufacturing challenges are prevalent such as high levels of raw material and process variability, difficulty characterising complex materials, and a lack of knowledge of critical process parameters and their effect on critical quality attributes of the viral vector and cell drug products. Multivariate data analysis (MVDA) has been leveraged successfully in a variety of applications in the chemical and biochemical industries, including for tasks such as bioprocess monitoring, identification of critical process parameters and assessment of process variability and comparability during process development, scale-up and technology transfer. Henceforth, MVDA is reviewed here as a suitable tool for tackling some of the challenges faced in the development of CGT manufacturing processes. A summary of some key CGT manufacturing challenges is provided along with a review of MVDA applications to mammalian and microbial processes, and an exploration of the potential benefits, requirements and pre-requisites of MVDA applications in the development of CGT manufacturing processes.
细胞基因治疗 (CGT) 的出现作为一种安全有效的治疗方法,针对许多严重的遗传性和获得性人类疾病,这引发了对新 CGT 产品的日益增长的兴趣和投资。这些产品中最成功的是基于自体病毒载体的治疗方法。病毒载体制造工艺和体外患者细胞处理能力的发展是推进基于自体病毒载体 CGT 治疗的紧迫问题。在病毒载体生产中,由于传统实验室系统的可扩展性有限,以及根据当前良好生产规范制造大量病毒载体的需求,扩大规模是一项关键任务。体外细胞处理方法需要进行优化和自动化,然后才能进行扩展,并且还存在其他几个制造挑战,例如原材料和工艺变异性水平高、难以对复杂材料进行特性分析,以及缺乏对关键工艺参数及其对病毒载体和细胞药物产品关键质量属性的影响的了解。多元数据分析 (MVDA) 在化学和生化工业的各种应用中已成功应用,包括用于生物工艺监测、识别关键工艺参数以及评估工艺变异性和可比性在工艺开发、放大和技术转让期间。因此,MVDA 在这里被视为解决 CGT 制造工艺开发中面临的一些挑战的合适工具。本文提供了一些关键 CGT 制造挑战的摘要,同时回顾了 MVDA 在哺乳动物和微生物工艺中的应用,并探讨了 MVDA 应用于 CGT 制造工艺开发的潜在益处、要求和前提条件。