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

被引:6
作者
Michaels, Yale S. [1 ,2 ,3 ]
Durland, Lauren J. [1 ]
Zandstra, Peter W. [1 ,4 ]
机构
[1] Univ British Columbia, Sch Biomed Engn, Vancouver, BC V6T 1Z3, Canada
[2] Univ Manitoba, Rady Fac Hlth Sci, Dept Biochem & Med Genet, Winnipeg, MB, Canada
[3] CancerCare Manitoba Res Inst, CancerCare Manitoba, Winnipeg, MB, Canada
[4] Univ British Columbia, Michael Smith Labs, Vancouver, BC, Canada
来源
GEN BIOTECHNOLOGY | 2023年 / 2卷 / 02期
关键词
HUMAN HEMATOPOIETIC STEM; NATURAL-KILLER-CELLS; PROGENITOR CELLS; YOLK-SAC; IN-VIVO; MYELOID PROGENITORS; CAR; DIFFERENTIATION; PRECURSORS; INDUCTION;
D O I
10.1089/genbio.2023.0008
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
引用
收藏
页码:106 / 119
页数:14
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