免疫原性细胞死亡
钙网蛋白
HMGB1
免疫系统
热休克蛋白
癌症研究
体外
电离辐射
细胞毒性T细胞
医学
生物
程序性细胞死亡
细胞生物学
免疫疗法
细胞凋亡
抗原
细胞
化学
免疫学
辐照
旁观者效应
免疫
炎症
生物化学
核物理学
内质网
物理
基因
作者
Mengqin Zhu,Mengdie Yang,Jiajia Zhang,Yuzhen Yin,Xin Fan,Yu Zhang,Shanshan Qin,Han Zhang,Fei Yu
标识
DOI:10.3389/fimmu.2021.705361
摘要
Immunogenic cell death (ICD) is a form of regulated cell death (RCD) induced by various stresses and produces antitumor immunity via damage-associated molecular patterns (DAMPs) release or exposure, mainly including high mobility group box 1 (HMGB1), calreticulin (CRT), adenosine triphosphate (ATP), and heat shock proteins (HSPs). Emerging evidence has suggested that ionizing radiation (IR) can induce ICD, and the dose, type, and fractionation of irradiation influence the induction of ICD. At present, IR-induced ICD is mainly verified in vitro in mice and there is few clinical evidence about it. To boost the induction of ICD by IR, some strategies have shown synergy with IR to enhance antitumor immune response, such as hyperthermia, nanoparticles, and chemotherapy. In this review, we focus on the molecular mechanisms of ICD, ICD-promoting factors associated with irradiation, the clinical evidence of ICD, and immunogenic forms of cell death. Finally, we summarize various methods of improving ICD induced by IR.
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