上睑下垂
生物
免疫系统
坏死性下垂
先天免疫系统
免疫
癌症研究
免疫学
效应器
获得性免疫系统
癌变
癌症
细胞
程序性细胞死亡
淋巴因子激活杀伤细胞
癌细胞
NK-92
免疫疗法
细胞毒性
免疫编辑
干扰素
肿瘤微环境
电池类型
肿瘤进展
先天性淋巴细胞
细胞免疫
T细胞
自然杀伤细胞
信号转导
细胞信号
免疫监视
细胞因子
细胞生物学
作者
Z Zhang,Judy Lieberman
标识
DOI:10.1146/annurev-immunol-082423-041848
摘要
The major effector cells of antitumor immunity are killer lymphocytes that recognize and eliminate tumor cells. The fact that tumor cells look a lot like normal cells poses a challenge to antitumor immune control. A danger signal from the tumor or from antigen-presenting cells that have taken up dying tumor cells is needed to distinguish tumor cells from normal cells to fully activate killer cell effector functionality and memory and thereby control the tumor. How a tumor cell dies strongly affects whether the immune system sees it as dangerous. Activation of innate immunity in the tumor, including interferon signaling and necrotic cell death (e.g., necroptosis and pyroptosis), sounds a potent immune alarm. Pyroptosis plays an important role in tumor immunity by generating an inflamed tumor microenvironment. However, it is a double-edged sword that can both promote tumorigenesis and increase the effectiveness and cytotoxicity of cancer therapy. In this article, we review what is known about the role of tumor cell pyroptosis, which is arguably the most inflammatory type of cell death, in antitumor immunity and discuss whether it could be safely harnessed to broaden the range of tumors that respond to immunotherapy.
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