Centre de Recherche en Cancérologie de Lyon, Lyon, France.
ErVaccine Technologies, Lyon, France.
Sci Adv. 2023 Feb 15;9(7):eadf3700. doi: 10.1126/sciadv.adf3700.
T cell engineering has changed the landscape of cancer immunotherapy. Chimeric antigen receptor T cells have demonstrated a remarkable efficacy in the treatment of B cell malignancies in hematology. However, their clinical impact on solid tumors has been modest so far. T cells expressing an engineered T cell receptor (TCR-T cells) represent a promising therapeutic alternative. The target repertoire is not limited to membrane proteins, and intrinsic features of TCRs such as high antigen sensitivity and near-to-physiological signaling may improve tumor cell detection and killing while improving T cell persistence. In this review, we present the clinical results obtained with TCR-T cells targeting different tumor antigen families. We detail the different methods that have been developed to identify and optimize a TCR candidate. We also discuss the challenges of TCR-T cell therapies, including toxicity assessment and resistance mechanisms. Last, we share some perspectives and highlight future directions in the field.
T 细胞工程改变了癌症免疫疗法的格局。嵌合抗原受体 T 细胞在血液学中治疗 B 细胞恶性肿瘤方面显示出了显著的疗效。然而,到目前为止,它们对实体肿瘤的临床影响还不大。表达工程化 T 细胞受体 (TCR-T 细胞) 的 T 细胞代表了一种有前途的治疗选择。靶标谱不仅限于膜蛋白,而且 TCR 的内在特征,如高抗原敏感性和近乎生理的信号转导,可能会提高肿瘤细胞的检测和杀伤能力,同时提高 T 细胞的持久性。在这篇综述中,我们介绍了针对不同肿瘤抗原家族的 TCR-T 细胞获得的临床结果。我们详细介绍了已经开发的用于识别和优化 TCR 候选物的不同方法。我们还讨论了 TCR-T 细胞疗法面临的挑战,包括毒性评估和耐药机制。最后,我们分享了一些观点,并强调了该领域的未来方向。