Köseer Ayse Sedef, Di Gaetano Simona, Arndt Claudia, Bachmann Michael, Dubrovska Anna
National Center for Tumor Diseases (NCT), Partner Site Dresden: German Cancer Research Center (DKFZ), Heidelberg, Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden, Helmholtz-Zentrum Dresden-Rossendorf (HZDR), 01307 Dresden, Germany.
OncoRay-National Center for Radiation Research in Oncology, Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden, Helmholtz-Zentrum Dresden-Rossendorf (HZDR), 01309 Dresden, Germany.
Cancers (Basel). 2023 Mar 5;15(5):1608. doi: 10.3390/cancers15051608.
The generally accepted view is that CSCs hijack the signaling pathways attributed to normal stem cells that regulate the self-renewal and differentiation processes. Therefore, the development of selective targeting strategies for CSC, although clinically meaningful, is associated with significant challenges because CSC and normal stem cells share many important signaling mechanisms for their maintenance and survival. Furthermore, the efficacy of this therapy is opposed by tumor heterogeneity and CSC plasticity. While there have been considerable efforts to target CSC populations by the chemical inhibition of the developmental pathways such as Notch, Hedgehog (Hh), and Wnt/β-catenin, noticeably fewer attempts were focused on the stimulation of the immune response by CSC-specific antigens, including cell-surface targets. Cancer immunotherapies are based on triggering the anti-tumor immune response by specific activation and targeted redirecting of immune cells toward tumor cells. This review is focused on CSC-directed immunotherapeutic approaches such as bispecific antibodies and antibody-drug candidates, CSC-targeted cellular immunotherapies, and immune-based vaccines. We discuss the strategies to improve the safety and efficacy of the different immunotherapeutic approaches and describe the current state of their clinical development.
普遍接受的观点是,癌症干细胞(CSC)劫持了归因于正常干细胞的信号通路,这些信号通路调节自我更新和分化过程。因此,开发针对CSC的选择性靶向策略虽然具有临床意义,但也面临重大挑战,因为CSC和正常干细胞在维持和存活方面共享许多重要的信号机制。此外,这种疗法的疗效受到肿瘤异质性和CSC可塑性的阻碍。虽然已经做出了相当大的努力,通过化学抑制Notch、Hedgehog(Hh)和Wnt/β-连环蛋白等发育途径来靶向CSC群体,但明显较少有人尝试通过CSC特异性抗原(包括细胞表面靶点)来刺激免疫反应。癌症免疫疗法基于通过特异性激活免疫细胞并将其靶向重定向至肿瘤细胞来触发抗肿瘤免疫反应。本综述聚焦于针对CSC的免疫治疗方法,如双特异性抗体和抗体-药物候选物、靶向CSC的细胞免疫疗法以及基于免疫的疫苗。我们讨论了提高不同免疫治疗方法安全性和疗效的策略,并描述了它们临床开发的现状。