Synthetic Biology in the Engineering of CAR-T and CAR-NK Cell Therapies: Facts and Hopes

被引:11
|
作者
Clubb, Justin D. [1 ]
Gao, Torahito A. [1 ]
Chen, Yvonne Y. [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biomol Engn, Los Angeles, CA USA
[2] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA USA
[3] UCLA, Parker Inst Canc Immunotherapy Ctr, Los Angeles, CA USA
[4] Univ Calif Los Angeles, 609 Charles E Young Dr, Los Angeles, CA 90095 USA
基金
美国国家科学基金会;
关键词
NATURAL-KILLER-CELLS; CHIMERIC ANTIGEN RECEPTORS; TGF-BETA RECEPTOR; ADOPTIVE TRANSFER; TUMOR-CELLS; IMMUNOTHERAPY; RECOGNITION; ACTIVATION; RESISTANT; EXPANSION;
D O I
10.1158/1078-0432.CCR-22-1491
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The advent of modern synthetic-biology tools has enabled the development of cellular treatments with engineered specificity, leading to a new paradigm in anticancer immunotherapy. T cells have been at the forefront of such development, with six chimeric antigen receptor-modified T-cell products approved by the FDA for the treatment of hematologic malignancies in the last 5 years. Natural killer (NK) cells are innate lymphocytes with potent cytotoxic activities, and they have become an increasingly attractive alternative to T-cell therapies due to their potential for allogeneic, "off-the-shelf" applications. However, both T cells and NK cells face numerous challenges, including antigen escape, the immunosuppressive tumor microenviron-ment, and potential for severe toxicity. Many synthetic-biology strategies have been developed to address these obstacles, most commonly in the T-cell context. In this review, we discuss the array of strategies developed to date, their application in the NK-cell context, as well as opportunities and challenges for clinical translation.
引用
收藏
页码:1390 / 1402
页数:13
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