Department of Haematooncology, Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.
Department of Haematooncology, University Hospital Ostrava, Ostrava, Czech Republic.
J Transl Med. 2023 Mar 15;21(1):197. doi: 10.1186/s12967-023-04041-6.
Cancer immunotherapies utilizing genetically engineered T cells have emerged as powerful personalized therapeutic agents showing dramatic preclinical and clinical results, particularly in hematological malignancies. Ectopically expressed chimeric antigen receptors (CARs) reprogram immune cells to target and eliminate cancer. However, CAR T cell therapy's success depends on the balance between effective anti-tumor activity and minimizing harmful side effects. To improve CAR T cell therapy outcomes and mitigate associated toxicities, scientists from different fields are cooperating in developing next-generation products using the latest molecular cell biology and synthetic biology tools and technologies. The immunotherapy field is rapidly evolving, with new approaches and strategies being reported at a fast pace. This comprehensive literature review aims to provide an up-to-date overview of the latest developments in controlling CAR T cell activity for improved safety, efficacy, and flexibility.
利用基因工程改造的 T 细胞的癌症免疫疗法已经成为强大的个性化治疗药物,在血液系统恶性肿瘤中显示出显著的临床前和临床效果。异位表达的嵌合抗原受体 (CAR) 可重新编程免疫细胞以靶向和消除癌症。然而,CAR T 细胞疗法的成功取决于有效抗肿瘤活性和最小化有害副作用之间的平衡。为了提高 CAR T 细胞疗法的效果并减轻相关毒性,来自不同领域的科学家正在合作,利用最新的分子细胞生物学和合成生物学工具和技术开发下一代产品。免疫疗法领域正在迅速发展,新的方法和策略正在快速报道。本综述旨在提供最新的关于控制 CAR T 细胞活性以提高安全性、疗效和灵活性的最新进展的概述。