Immunology Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, Vic., Australia.
The Department of Medical Biology, The University of Melbourne, Parkville, Vic., Australia.
Mol Oncol. 2023 Jun;17(6):946-949. doi: 10.1002/1878-0261.13420. Epub 2023 Apr 1.
Synthetic biology has made it possible to rewire natural cellular responses to treat disease, notably demonstrated by chimeric antigen receptor (CAR) T cells as cancer immunotherapy. Building on the success of T-cell activation using synthetic receptors, the field is now investigating how induction of noncanonical signalling pathways and sophisticated synthetic gene circuitry can enhance the antitumour phenotype of engineered T cells. This commentary explores two recently published studies that provide proof of concept for how new technologies achieve this. The first demonstrated that non-naturally occurring combinations of signalling motifs derived from various immune receptors and arranged as a CAR drove unique signal transduction pathways in T cells and improved their tumour killing ability. Here, machine learning complemented the screening process and successfully predicted CAR T-cell phenotype dependent on signalling motif choice. The second explored how synthetic zinc fingers can be engineered into controllable transcriptional regulators, where their activity was dependent on the presence or absence of FDA-approved small-molecule drugs. These studies are pivotal in expanding the design choices available for gene circuits of the future and highlight how a single cellular therapy could respond to multiple environmental cues including target cell antigen expression, the tumour microenvironment composition and small molecule drugs.
合成生物学使得对天然细胞反应进行重新布线以治疗疾病成为可能,这在嵌合抗原受体(CAR)T 细胞作为癌症免疫疗法中得到了显著证明。在使用合成受体激活 T 细胞取得成功的基础上,该领域目前正在研究如何诱导非规范信号通路和复杂的合成基因电路,以增强工程化 T 细胞的抗肿瘤表型。这篇评论探讨了最近发表的两项研究,这些研究为新技术如何实现这一目标提供了概念验证。第一项研究表明,源自各种免疫受体的信号基序的非天然组合,并排列为 CAR,可在 T 细胞中驱动独特的信号转导途径,并提高其肿瘤杀伤能力。在这里,机器学习补充了筛选过程,并成功预测了依赖于信号基序选择的 CAR T 细胞表型。第二项研究探索了如何将合成锌指工程设计成可控的转录调节剂,其活性取决于 FDA 批准的小分子药物的存在或不存在。这些研究对于扩展未来基因电路的设计选择至关重要,并强调了单一细胞疗法如何对多种环境线索做出反应,包括靶细胞抗原表达、肿瘤微环境组成和小分子药物。