Department of Gastrointestinal and Colorectal Surgery, China-Japan Union Hospital of Jilin University, Changchun, 130033, People's Republic of China.
Int J Nanomedicine. 2024 Jun 10;19:5545-5579. doi: 10.2147/IJN.S457309. eCollection 2024.
Pyroptosis, a pro-inflammatory and lytic programmed cell death pathway, possesses great potential for antitumor immunotherapy. By releasing cellular contents and a large number of pro-inflammatory factors, tumor cell pyroptosis can promote dendritic cell maturation, increase the intratumoral infiltration of cytotoxic T cells and natural killer cells, and reduce the number of immunosuppressive cells within the tumor. However, the efficient induction of pyroptosis and prevention of damage to normal tissues or cells is an urgent concern to be addressed. Recently, a wide variety of nanoplatforms have been designed to precisely trigger pyroptosis and activate the antitumor immune responses. This review provides an update on the progress in nanotechnology for enhancing pyroptosis-based tumor immunotherapy. Nanomaterials have shown great advantages in triggering pyroptosis by delivering pyroptosis initiators to tumors, increasing oxidative stress in tumor cells, and inducing intracellular osmotic pressure changes or ion imbalances. In addition, the challenges and future perspectives in this field are proposed to advance the clinical translation of pyroptosis-inducing nanomedicines.
细胞焦亡,一种促炎和裂解的程序性细胞死亡途径,在抗肿瘤免疫治疗方面具有巨大潜力。肿瘤细胞焦亡通过释放细胞内容物和大量促炎因子,促进树突状细胞成熟,增加肿瘤内细胞毒性 T 细胞和自然杀伤细胞的浸润,减少肿瘤内的免疫抑制细胞数量。然而,如何高效诱导细胞焦亡并防止对正常组织或细胞造成损伤是一个亟待解决的问题。最近,设计了多种纳米平台来精确触发细胞焦亡并激活抗肿瘤免疫反应。本综述介绍了纳米技术在增强基于细胞焦亡的肿瘤免疫治疗方面的最新进展。纳米材料在通过将细胞焦亡诱导剂递送至肿瘤、增加肿瘤细胞内氧化应激以及诱导细胞内渗透压变化或离子失衡来触发细胞焦亡方面显示出巨大优势。此外,还提出了该领域的挑战和未来展望,以推进诱导细胞焦亡的纳米药物的临床转化。
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