Hunt Charles J
Sawston, United Kingdom.
Transfus Med Hemother. 2019 Jun;46(3):134-150. doi: 10.1159/000497289. Epub 2019 Mar 28.
The commercial and clinical development of cellular therapy products will invariably require cryopreservation and frozen storage of cellular starting materials, intermediates and/or final product. Optimising cryopreservation is as important as optimisation of the cell culture process in obtaining maximum yield and a consistent end-product. Suboptimal cryopreservation can lead not only to batch-to-batch variation, lowered cellular functionality and reduced cell yield, but also to the potential selection of subpopulations with genetic or epigenetic characteristics divergent from the original cell line. Regulatory requirements also impact on cryopreservation as these will require a robust and reproducible approach to the freezing, storage and thawing of the product. This requires attention to all aspects of the application of low temperatures: from the choice of freezing container and cryoprotectant, the cooling rate employed and its mode of de-livery, the correct handling of the frozen material during storage and transportation, to the eventual thawing of the product by the end-user. Each of these influences all of the others to a greater or lesser extent and none should be ignored. This paper seeks to provide practical insights and alternative solutions to the technical challenges faced during cryopreservation of cells for use in cellular therapies.
细胞治疗产品的商业和临床开发必然需要对细胞起始材料、中间体和/或最终产品进行冷冻保存和冻存。在获得最大产量和一致的最终产品方面,优化冷冻保存与优化细胞培养过程同样重要。次优的冷冻保存不仅会导致批次间差异、细胞功能降低和细胞产量减少,还可能导致选择出具有与原始细胞系不同的遗传或表观遗传特征的亚群。监管要求也会对冷冻保存产生影响,因为这些要求需要一种稳健且可重复的产品冷冻、储存和解冻方法。这需要关注低温应用的各个方面:从冷冻容器和冷冻保护剂的选择、所采用的冷却速率及其传递方式、在储存和运输过程中对冷冻材料的正确处理,到最终用户对产品的解冻。这些因素中的每一个都会在或大或小的程度上影响其他因素,任何一个都不应被忽视。本文旨在为细胞治疗中细胞冷冻保存过程中面临的技术挑战提供实用见解和替代解决方案。