Yamazaki Takahiro, Vanpouille-Box Claire, Demaria Sandra, Galluzzi Lorenzo
Department of Radiation Oncology, Weill Cornell Medical College, New York, NY, USA.
Sandra and Edward Meyer Cancer Center, New York, NY, USA.
Cancer Treat Res. 2020;180:281-296. doi: 10.1007/978-3-030-38862-1_10.
Immunogenic cell death (ICD) is a particular form of cell death that can initiate adaptive immunity against antigens expressed by dying cells in the absence of exogenous adjuvants. This implies that cells undergoing ICD not only express antigens that are not covered by thymic tolerance, but also deliver adjuvant-like signals that enable the recruitment and maturation of antigen-presenting cells toward an immunostimulatory phenotype, culminating with robust cross-priming of antigen-specific CD8 T cells. Such damage-associated molecular patterns (DAMPs), which encompass cellular proteins, small metabolites and cytokines, are emitted in a spatiotemporally defined manner in the context of failing adaptation to stress. Radiation therapy (RT) is a bona fide inducer of ICD, at least when employed according to specific doses and fractionation schedules. Here, we discuss the mechanisms whereby DAMPs emitted by cancer cells undergoing RT-driven ICD alter the functional configuration of the tumor microenvironment.
免疫原性细胞死亡(ICD)是一种特殊形式的细胞死亡,在没有外源性佐剂的情况下,它可以启动针对死亡细胞所表达抗原的适应性免疫。这意味着经历ICD的细胞不仅表达未被胸腺耐受性覆盖的抗原,还传递类似佐剂的信号,使抗原呈递细胞募集并成熟为免疫刺激性表型,最终实现抗原特异性CD8 T细胞的强大交叉启动。这种损伤相关分子模式(DAMPs),包括细胞蛋白、小分子代谢产物和细胞因子,在无法适应应激的情况下以时空限定的方式释放。放射治疗(RT)是ICD的一种真正诱导剂,至少在按照特定剂量和分割方案使用时是如此。在这里,我们讨论了经历RT驱动的ICD的癌细胞释放的DAMPs改变肿瘤微环境功能结构的机制。