免疫原性细胞死亡
免疫疗法
癌症
钙网蛋白
免疫系统
癌症免疫疗法
癌细胞
程序性细胞死亡
癌症研究
树突状细胞
医学
免疫学
生物
细胞凋亡
细胞生物学
内科学
内质网
生物化学
作者
Haolong Qi,Yuan Li,Yingjie Geng,Xinhuan Wan,Xiaoqing Cai
标识
DOI:10.1016/j.ijpharm.2024.124045
摘要
The field of cancer therapy is witnessing the emergence of immunotherapy, an innovative approach that activates the body own immune system to combat cancer. Immunogenic cell death (ICD) has emerged as a prominent research focus in the field of cancer immunotherapy, attracting significant attention in recent years. The activation of ICD can induce the release of damage-associated molecular patterns (DAMPs), such as calreticulin (CRT), adenosine triphosphate (ATP), high mobility group box protein 1 (HMGB1), and heat shock proteins (HSP). Subsequently, this process promotes the maturation of innate immune cells, including dendritic cells (DCs), thereby triggering a T cell-mediated anti-tumor immune response. The activation of the ICD ultimately leads to the development of long-lasting immune responses against tumors. Studies have demonstrated that partial therapeutic approaches, such as chemotherapy with doxorubicin, specific forms of radiotherapy, and phototherapy, can induce the generation of ICD. The main focus of this article is to discuss and review the therapeutic methods triggered by nanoparticles for ICD, while briefly outlining their anti-tumor mechanism. The objective is to provide a comprehensive reference for the widespread application of ICD.
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