Cheng Quansheng, Zhang Tesen, Wang Qingcheng, Wu Xue, Li Lingyun, Lin Runxing, Zhou Yinning, Qu Songnan
Joint Key Laboratory of the Ministry of Education, Institute of Applied Physics and Materials Engineering, University of Macau, Taipa, Macau, SAR, 999078, China.
Department of Physics and Chemistry, Faculty of Science and Technology, University of Macau, Taipa, Macau, SAR, 999078, China.
Adv Mater. 2024 Sep;36(39):e2408685. doi: 10.1002/adma.202408685. Epub 2024 Aug 12.
Manufacturing whole cancer cell vaccines (WCCV) with both biosafety and efficacy is crucial for tumor immunotherapy. Pyroptotic cancer cells, due to their highly immunogenic properties, present a promising avenue for the development of WCCV. However, the successful development of WCCV based on pyroptotic cancer cells is yet to be accomplished. Here, a facile strategy that utilized photocatalytic carbon dots (CDs) to induce pyroptosis of cancer cells for fabricating WCCV is reported. Photocatalytic CDs are capable of generating substantial amounts of hydroxyl radicals and can effectively decrease cytoplasmic pH values under white light irradiation. This process efficiently triggers cancer cell pyroptosis through the reactive oxygen species (ROS)-mitochondria-caspase 3-gasdermin E pathway and the proton motive force-driven mitochondrial ATP synthesis pathway. Moreover, in vitro, these photocatalytic CDs-induced pyroptotic cancer cells (PCIP) can hyperactivate macrophage (M0-M1) with upregulation of major histocompatibility complex class II expression. In vivo, PCIP induced specific immune-preventive effects in melanoma and breast cancer mouse models through anticancer immune memory, demonstrating effective WCCV. This work provides novel insights for inducing cancer cell pyroptosis and bridges the gap in the fabrication of WCCV based on pyroptotic cancer cells.
制造兼具生物安全性和有效性的全癌细胞疫苗(WCCV)对于肿瘤免疫治疗至关重要。由于其高度免疫原性,焦亡癌细胞为WCCV的开发提供了一条有前景的途径。然而,基于焦亡癌细胞的WCCV的成功开发尚未实现。在此,报道了一种利用光催化碳点(CDs)诱导癌细胞焦亡以制造WCCV的简便策略。光催化CDs能够产生大量羟基自由基,并能在白光照射下有效降低细胞质pH值。该过程通过活性氧(ROS)-线粒体-半胱天冬酶3- Gasdermin E途径和质子动力驱动的线粒体ATP合成途径有效触发癌细胞焦亡。此外,在体外,这些光催化CDs诱导的焦亡癌细胞(PCIP)可通过上调主要组织相容性复合体II类表达使巨噬细胞(M0-M1)过度活化。在体内,PCIP通过抗癌免疫记忆在黑色素瘤和乳腺癌小鼠模型中诱导特异性免疫预防作用,证明了WCCV的有效性。这项工作为诱导癌细胞焦亡提供了新的见解,并填补了基于焦亡癌细胞的WCCV制造方面的空白。