Department of Radiation Oncology, Weill Cornell Medical College, New York, NY, USA.
Sandra and Edward Meyer Cancer Center, New York, NY, USA.
Nat Rev Drug Discov. 2024 Jun;23(6):445-460. doi: 10.1038/s41573-024-00920-9. Epub 2024 Apr 15.
Immunogenic cell death (ICD), which results from insufficient cellular adaptation to specific stressors, occupies a central position in the development of novel anticancer treatments. Several therapeutic strategies to elicit ICD - either as standalone approaches or as means to convert immunologically cold tumours that are insensitive to immunotherapy into hot and immunotherapy-sensitive lesions - are being actively pursued. However, the development of ICD-inducing treatments is hindered by various obstacles. Some of these relate to the intrinsic complexity of cancer cell biology, whereas others arise from the use of conventional therapeutic strategies that were developed according to immune-agnostic principles. Moreover, current discovery platforms for the development of novel ICD inducers suffer from limitations that must be addressed to improve bench-to-bedside translational efforts. An improved appreciation of the conceptual difference between key factors that discriminate distinct forms of cell death will assist the design of clinically viable ICD inducers.
免疫原性细胞死亡(ICD)是由于细胞对特定应激原的适应不足而产生的,在新型抗癌治疗的发展中占据核心地位。目前正在积极探索几种引发 ICD 的治疗策略——无论是作为独立的方法,还是作为将对免疫疗法不敏感的免疫冷肿瘤转化为对免疫疗法敏感的热肿瘤的手段。然而,ICD 诱导治疗的发展受到各种障碍的阻碍。其中一些与癌细胞生物学的内在复杂性有关,而另一些则源于根据免疫不可知原则开发的传统治疗策略的使用。此外,目前用于开发新型 ICD 诱导剂的发现平台存在局限性,必须加以解决,以改善从实验室到临床的转化工作。更好地理解区分不同形式细胞死亡的关键因素之间的概念差异,将有助于设计临床上可行的 ICD 诱导剂。