Manufacturing of Large Numbers of Patient-specific T Cells for Adoptive Immunotherapy

单采 离体 低温保存 外周血单个核细胞 免疫疗法 细胞疗法 医学 T细胞 免疫学 体内 免疫系统 过继性细胞移植 细胞 化学 体外 生物 生物技术 细胞生物学 血小板 胚胎 生物化学
作者
Chy-Anh Tran,Luciana Burton,Diana Russom,Jamie R. Wagner,Michael C. Jensen,Stephen J. Forman,David DiGiusto
出处
期刊:Journal of Immunotherapy [Ovid Technologies (Wolters Kluwer)]
卷期号:30 (6): 644-654 被引量:41
标识
DOI:10.1097/cji.0b013e318052e1f4
摘要

We have developed an innovative system for ex vivo processing of patient-specific cell products to produce large numbers of T-lymphocytes in support of phase 2 adoptive immunotherapy trials for hematologic malignancies. Extensive efforts were undertaken to close the cell processing system to improve the safety profile of the process and comply with new federal regulations regarding cell and tissue processing. Our results demonstrate that apheresis products can be processed in a closed system (Cytomate) with similar yields (≈4×109 mononuclear cells/apheresis) and recoveries (≈60% of starting mononuclear cells) to manual cell processing. Cells processed with this system could be cryopreserved for up to 5 months without significant loss of recovery or viability. Additionally, we have evaluated the use of gas permeable bags and developed perfusion bioreactor protocols in which T cells can be rapidly produced in excess of 1010 viable cells per liter of culture. Using similar methods for upfront processing, we have also developed methods for positive selection and ex vivo culture of CD4+ T cells that result in 200 to 800-fold expansion of fresh or cryopreserved samples. T cells produced in these systems were shown to retain activation-induced cytolytic capability and TH1/TH2 cytokine production as a measure of biologic potency. These new methods allow for more efficient production multiple patient-specific products by satisfying the basic tenants of safety and efficacy required for early phase clinical trials of cell products.
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