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开发用于癌症免疫治疗的 CD8 细胞毒性 T 细胞快速扩增的离心生物反应器

英文原题:Development of a centrifugal bioreactor for rapid expansion of CD8 cytotoxic T cells for use in cancer immunotherapy.

查看英文原题

Development of a centrifugal bioreactor for rapid expansion of CD8 cytotoxic T cells for use in cancer immunotherapy.

PubMed 2023/09/11(内容时间) Biotechnol Prog Q3 · IF 2.8(JCR 2025)

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中文摘要

目前限制过继性细胞疗法(ACT)用于癌症治疗的困难之一是缺乏快速扩增T细胞的方法。如本报告所述,我们开发了一种离心生物反应器(CBR),可能解决这一制造瓶颈。CBR通过平衡离心力与新鲜培养基的连续进料以灌注方式运行,防止细胞离开扩增培养室,同时维持生长所需的营养物质。使用一种对感染原生动物寄生虫Theileria parva的自体靶细胞具有特异性的牛CD8细胞毒性T淋巴细胞(CTL)细胞系,来确定CBR用于ACT目的的功效。进行了批次培养实验,以预测CTL如何响应与营养物质消耗和有毒代谢物(如铵和乳酸)产生相关的环境变化。这些研究的数据被用于开发动力学生长模型,使我们能够预测CBR中CTL的生长并确定最佳操作参数。该模型预测,在单个11-mL锥形室中,CBR可维持的最大细胞密度为5.5 × 10 7 cells/mL,氧气是限制因素。在CBR中扩增CTL的实验结果与动力学模型有95%的一致性。本报告中描述的原型CBR可用于开发用于癌症免疫治疗的CBR。

展开英文摘要原文

One of the current difficulties limiting the use of adoptive cell therapy (ACT) for cancer treatment is the lack of methods for rapidly expanding T cells. As described in the present report, we developed a centrifugal bioreactor (CBR) that may resolve this manufacturing bottleneck. The CBR operates in perfusion by balancing centrifugal forces with a continuous feed of fresh medium, preventing cells from leaving the expansion culture chamber while maintaining nutrients for growth. A bovine CD8 cytotoxic T lymphocyte (CTL) cell line specific for an autologous target cell infected with a protozoan parasite, Theileria parva, was used to determine the efficacy of the CBR for ACT purposes.

Batch culture experiments were conducted to predict how CTLs respond to environmental changes associated with consumption of nutrients and production of toxic metabolites, such as ammonium and lactate. Data from these studies were used to develop a kinetic growth model, allowing us to predict CTL growth in the CBR and determine the optimal operating parameters.

The model predicts the maximum cell density the CBR can sustain is 5. 5 × 10 7 cells/mL in a single 11-mL conical chamber with oxygen being the limiting factor. Experimental results expanding CTLs in the CBR are in 95% agreement with the kinetic model. The prototype CBR described in this report can be used to develop a CBR for use in cancer immunotherapy.

论文信息

作者
Kaiphanliam KM、Fraser-Hevlin B、Barrow ES、Davis WC、Van Wie BJ
单位
Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, Washington, USA.United States
文献类型
美国政府(非公共卫生署)资助研究 · 非美国政府资助研究
期刊
Biotechnology progress2023 Nov-Dec
原文标识
PubMed 37694563 · DOI 10.1002/btpr.3388