Clinical Research Division and Program in Immunology, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave N, Seattle, WA 98109, USA.
Clinical Research Division and Program in Immunology, Fred Hutchinson Cancer Research Center, 1100 Fairview Ave N, Seattle, WA 98109, USA.
Trends Cancer. 2021 Jan;7(1):48-56. doi: 10.1016/j.trecan.2020.09.002. Epub 2020 Sep 26.
Adoptively transferred T cell receptor (TCR)-transgenic T cells (TCR-T cells) are not restricted by cell surface expression of their targets and are therefore poised to become a main pillar of cellular cancer immunotherapies. Addressing clinical and laboratory data, we discuss emerging features for the efficient deployment of novel TCR-T therapies, such as selection of ideal TCRs targeting validated epitopes with well-characterized cancer cell expression and processing, enhancing TCR-T effector function, trafficking, expansion, persistence, and memory formation by strategic selection of substrate cells, and gene-engineering with synthetic co-stimulatory circuits. Overall, a better understanding of the relevant mechanisms of action and resistance will help prioritize the vast array of potential TCR-T optimizations for future clinical products.
过继性转移的 T 细胞受体 (TCR)-转基因 T 细胞 (TCR-T 细胞) 不受其靶细胞表面表达的限制,因此有望成为细胞癌症免疫疗法的主要支柱。根据临床和实验室数据,我们讨论了有效部署新型 TCR-T 疗法的新特征,例如选择针对具有明确肿瘤细胞表达和加工特征的已验证表位的理想 TCR,通过策略性选择基质细胞来增强 TCR-T 效应功能、归巢、扩增、持久性和记忆形成,以及通过合成共刺激回路进行基因工程。总的来说,更好地了解相关作用机制和耐药性将有助于为未来的临床产品确定大量潜在的 TCR-T 优化方案的优先级。