Center for Cellular Immunotherapies, Abramson Cancer Center and the Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Gene Ther. 2018 Jun;25(3):165-175. doi: 10.1038/s41434-018-0007-x. Epub 2018 Jun 7.
FDA approval of chimeric antigen receptor T cells (CART cells) is the culmination of several decades of technology development and interrogation of the properties of these gene therapies. CART cells exist as personalized "living drugs" and have demonstrated astounding anti-tumor efficacy in patients with leukemia and lymphoma. However, the future promise of CART efficacy for solid tumors, the greatest unmet burden, is met with a number of challenges that must be surmounted for effective immune responses. In this review, we discuss the next-generation developments of CARs to target solid tumors, including fine-tuned and combinational-targeting receptors. We consider the structural intricacies of the CAR molecules that influence optimal signaling and CART survival, and review pre-clinical cell-intrinsic and cell-extrinsic combinational therapy approaches.
FDA 批准嵌合抗原受体 T 细胞(CART 细胞)是几十年技术发展和对这些基因治疗特性的研究的结果。CART 细胞作为个性化的“活药物”存在,已在白血病和淋巴瘤患者中显示出惊人的抗肿瘤疗效。然而,CART 对实体瘤(最大的未满足需求)的疗效的未来前景面临着许多挑战,这些挑战必须克服,才能产生有效的免疫反应。在这篇综述中,我们讨论了针对实体瘤的 CAR 的下一代发展,包括微调的和组合靶向受体。我们考虑了影响最佳信号转导和 CART 存活的 CAR 分子的结构复杂性,并回顾了临床前细胞内和细胞外组合治疗方法。