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工程化 T 细胞发育以实现下一代干细胞衍生免疫疗法

英文原题:Engineering T Cell Development for the Next Generation of Stem Cell-Derived Immunotherapies.

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Engineering T Cell Development for the Next Generation of Stem Cell-Derived Immunotherapies.

PubMed 2023/04/18(内容时间) GEN Biotechnol Q3 · IF 2.1(JCR 2025)

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中文摘要

工程化T细胞处于临床细胞治疗的前沿。T细胞疗法已对部分血液系统恶性肿瘤患者的诊疗产生了显著影响。这一基础推动了针对广泛毁灭性适应症的即用型工程化细胞疗法的开发。实现这一愿景将需要以成本效益高的方式制造精准细胞产品,能够应对多重工艺和临床设计挑战。多能干细胞(PSC)来源的工程化T细胞正逐渐成为首选解决方案。为充分释放PSC来源T细胞疗法的潜力,该领域将需要能够稳健协调一系列复杂的、依赖于时间和剂量的信号事件的技术,这些信号事件是在实验室中重建功能性T细胞发育所必需的。在本文中,我们综述了同种异体T细胞疗法的当前状况,重点关注从PSC生成工程化淋巴细胞的策略。我们重点介绍了该领域近期令人振奋的进展,并概述了及时的发展机遇,重点强调微环境工程和合成生物学。

展开英文摘要原文

Engineered T cells are at the leading edge of clinical cell therapy. T cell therapies have had a remarkable impact on patient care for a subset of hematological malignancies. This foundation has motivated the development of off-the-shelf engineered cell therapies for a broad range of devastating indications. Achieving this vision will require cost-effective manufacturing of precision cell products capable of addressing multiple process and clinical-design challenges.

Pluripotent stem cell (PSC)-derived engineered T cells are emerging as a solution of choice. To unleash the full potential of PSC-derived T cell therapies, the field will require technologies capable of robustly orchestrating the complex series of time- and dose-dependent signaling events needed to recreate functional T cell development in the laboratory. In this article, we review the current state of allogenic T cell therapies, focusing on strategies to generate engineered lymphoid cells from PSCs.

We highlight exciting recent progress in this field and outline timely opportunities for advancement with an emphasis on niche engineering and synthetic biology.

论文信息

作者
Michaels YS、Durland LJ、Zandstra PW
单位
School of Biomedical Engineering, University of British Columbia, Vancouver, Canada; University of British Columbia, Vancouver, Canada.Canada
文献类型
综述
期刊
GEN biotechnology2023 Apr 1
原文标识
PubMed 37928777 · DOI 10.1089/genbio.2023.0008