Vandenabeele Peter, Vandecasteele Katrien, Bachert Claus, Krysko Olga, Krysko Dmitri V
Molecular Signalling and Cell Death Unit, Inflammation Research Center, VIB, Ghent, Belgium.
Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Adv Exp Med Biol. 2016;930:133-49. doi: 10.1007/978-3-319-39406-0_6.
For many years it has been thought that apoptotic cells rapidly cleared by phagocytic cells do not trigger an immune response but rather have anti-inflammatory properties. However, accumulating experimental data indicate that certain anticancer therapies can induce an immunogenic form of apoptosis associated with the emission of damage-associated molecular patterns (DAMPs), which function as adjuvants to activate host antitumor immune responses. In this review, we will first discuss recent advances and the significance of danger signaling pathways involved in the emission of DAMPs, including calreticulin, ATP, and HMGB1. We will also emphasize that switching on a particular signaling pathway depends on the immunogenic cell death stimulus. Further, we address the role of ER stress in danger signaling and the classification of immunogenic cell death inducers in relation to how ER stress is triggered. In the final part, we discuss the role of radiotherapy-induced immunogenic apoptosis and the relationship of its immunogenicity to the fraction dose and concomitant chemotherapy.
多年来,人们一直认为被吞噬细胞迅速清除的凋亡细胞不会引发免疫反应,反而具有抗炎特性。然而,越来越多的实验数据表明,某些抗癌疗法可诱导与损伤相关分子模式(DAMPs)释放相关的免疫原性凋亡形式,这些DAMPs可作为佐剂激活宿主抗肿瘤免疫反应。在本综述中,我们将首先讨论与DAMPs释放相关的危险信号通路的最新进展及其意义,包括钙网蛋白、ATP和高迁移率族蛋白B1(HMGB1)。我们还将强调,特定信号通路的开启取决于免疫原性细胞死亡刺激。此外,我们将探讨内质网应激在危险信号中的作用以及免疫原性细胞死亡诱导剂与内质网应激触发方式相关的分类。在最后一部分,我们将讨论放疗诱导的免疫原性凋亡的作用及其免疫原性与分次剂量和同步化疗的关系。