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用于大规模、高质量生产人T细胞的新型生物制造平台。

Novel biomanufacturing platform for large-scale and high-quality human T cells production.

作者信息

Ou Jianfa, Si Yingnan, Tang Yawen, Salzer Grace E, Lu Yun, Kim Seulhee, Qin Hongwei, Zhou Lufang, Liu Xiaoguang

机构信息

1Department of Biomedical Engineering, University of Alabama at Birmingham (UAB), 1670 University Blvd, Birmingham, AL 35233 USA.

2Department of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham (UAB), 1670 University Blvd, Birmingham, AL 35233 USA.

出版信息

J Biol Eng. 2019 Apr 23;13:34. doi: 10.1186/s13036-019-0167-2. eCollection 2019.

DOI:10.1186/s13036-019-0167-2
PMID:31044002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6480708/
Abstract

The adoptive transfer of human T cells or genetically-engineered T cells with cancer-targeting receptors has shown tremendous promise for eradicating tumors in clinical trials. The objective of this study was to develop a novel T cell biomanufacturing platform using stirred-tank bioreactor for large-scale and high-quality cellular production. First, various factors, such as bioreactor parameters, media, supplements, stimulation, seed age, and donors, were investigated. A serum-free fed-batch bioproduction process was developed to achieve 1000-fold expansion within 8 days after first stimulation and another 500-fold expansion with second stimulation. Second, this biomanufacturing process was successfully scaled up in bioreactor with dilution factor of 10, and the robustness and reproducibility of the process was confirmed by the inclusion of different donors' T cells of various qualities. Finally, T cell quality was monitored using 12 surface markers and 3 intracellular cytokines as the critical quality assessment criteria in early, middle and late stages of cell production. In this study, a new biomanufacturing platform was created to produce reliable, reproducible, high-quality, and large-quantity (i.e. > 5 billion) human T cells in stirred-tank bioreactor. This platform is compatible with the production systems of monoclonal antibodies, vaccines, and other therapeutic cells, which provides not only the proof-of-concept but also the ready-to-use new approach of T cell expansion for clinical immune therapy.

摘要

在临床试验中,过继转移具有癌症靶向受体的人T细胞或基因工程T细胞已显示出根除肿瘤的巨大潜力。本研究的目的是开发一种新型的T细胞生物制造平台,该平台使用搅拌罐生物反应器进行大规模、高质量的细胞生产。首先,研究了各种因素,如生物反应器参数、培养基、补充剂、刺激、种子代数和供体。开发了一种无血清补料分批生物生产工艺,以在首次刺激后8天内实现1000倍的扩增,并在第二次刺激后再实现500倍的扩增。其次,该生物制造工艺在稀释因子为10的生物反应器中成功放大,并且通过纳入不同质量的不同供体的T细胞,证实了该工艺的稳健性和可重复性。最后,在细胞生产的早期、中期和后期,使用12种表面标志物和3种细胞内细胞因子作为关键质量评估标准来监测T细胞质量。在本研究中,创建了一个新的生物制造平台,以在搅拌罐生物反应器中生产可靠、可重复、高质量和大量(即>50亿)的人T细胞。该平台与单克隆抗体、疫苗和其他治疗性细胞的生产系统兼容,这不仅提供了概念验证,还为临床免疫治疗提供了现成的T细胞扩增新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b586/6480708/456f4593a1d5/13036_2019_167_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b586/6480708/8cb112925927/13036_2019_167_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b586/6480708/a83ee89bd019/13036_2019_167_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b586/6480708/ed8d3975ab64/13036_2019_167_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b586/6480708/9d3630bf6a45/13036_2019_167_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b586/6480708/456f4593a1d5/13036_2019_167_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b586/6480708/8cb112925927/13036_2019_167_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b586/6480708/a83ee89bd019/13036_2019_167_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b586/6480708/ed8d3975ab64/13036_2019_167_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b586/6480708/9d3630bf6a45/13036_2019_167_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b586/6480708/456f4593a1d5/13036_2019_167_Fig5_HTML.jpg

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