Rane Riley, Li Fengqiao, Williams Alexis, Jayadev Avaneesh, Tran Nhan L, Winkles Jeffrey A, Kim Gloria B
Department of Physiology and Biomedical Engineering, Mayo Clinic Arizona, Scottsdale, AZ, United States.
Department of Immunology, Mayo Clinic Arizona, Scottsdale, AZ, United States.
Front Immunol. 2025 Oct 8;16:1662238. doi: 10.3389/fimmu.2025.1662238. eCollection 2025.
Adoptive T cell therapy has transformed cancer treatment, with chimeric antigen receptor (CAR) T cell therapy demonstrating remarkable clinical success in hematological malignancies. By genetically engineering a patient's own T cells to recognize and attack cancer cells, CAR T therapy has achieved durable remissions in several blood cancers. However, its efficacy in solid tumors remains limited, largely due to the immunosuppressive tumor microenvironment (TME), which impairs T cell infiltration, persistence, and function. To address these challenges, innovative strategies are being developed to reprogram T cell signaling within the hostile TME. One promising class involves chimeric non-antigen receptors (CNARs), which modulate T cell activity independently of direct antigen recognition. Among these, chimeric switch receptors (CSRs) convert inhibitory checkpoint signals into activating cues, while inverted cytokine receptors (ICRs) redirect suppressive cytokine signals to promote T cell activation. In this review, we provide a focused overview of the design principles, mechanistic functions, and therapeutic potentials of CSRs and ICRs as adjuncts to CAR T therapy in solid tumors. We also discuss key considerations regarding safety, specificity, and clinical translation to inform future advancements in engineered receptor strategies for cancer immunotherapy.
过继性T细胞疗法已经改变了癌症治疗方式,嵌合抗原受体(CAR)T细胞疗法在血液系统恶性肿瘤中显示出显著的临床成功。通过对患者自身的T细胞进行基因工程改造,使其识别并攻击癌细胞,CAR T疗法已在多种血液癌症中实现了持久缓解。然而,其在实体瘤中的疗效仍然有限,这在很大程度上是由于免疫抑制性肿瘤微环境(TME),它会损害T细胞的浸润、存活和功能。为应对这些挑战,正在开发创新策略来在恶劣的TME中重新编程T细胞信号传导。一类很有前景的策略涉及嵌合非抗原受体(CNAR),它独立于直接抗原识别来调节T细胞活性。其中,嵌合开关受体(CSR)将抑制性检查点信号转化为激活信号,而反向细胞因子受体(ICR)将抑制性细胞因子信号重定向以促进T细胞激活。在这篇综述中,我们重点概述了CSR和ICR作为CAR T疗法辅助手段在实体瘤中的设计原则、机制功能和治疗潜力。我们还讨论了关于安全性、特异性和临床转化的关键考虑因素,以为癌症免疫治疗工程受体策略的未来进展提供参考。