免疫原性细胞死亡
癌症研究
免疫疗法
吴茱萸碱
体内
光动力疗法
钙网蛋白
肿瘤微环境
细胞毒性
细胞凋亡
乳腺癌
医学
化疗
体外
癌细胞
癌症免疫疗法
程序性细胞死亡
转移
免疫系统
树突状细胞
癌症
细胞
T细胞
获得性免疫系统
细胞疗法
腺苷
化学
内科学
生物反应调节剂
药理学
免疫学
渗透(HVAC)
生物
作者
Qiang Zhou,Kui Wang,Dahong Yang,Yue Huang,Mengjun Yu,Dandan Xie,Jia Wang,Shiwen Chen,Jing Gong,Min Yang,Yu Zhao,Junfu Huang
标识
DOI:10.1002/adhm.202503039
摘要
Immunotherapy is a promising treatment for triple-negative breast cancer (TNBC), but the immunosuppressive tumor microenvironment (TME) compromises its efficacy. Therefore, the nano-drug TPGS@EVO/Ppa (TEP) is designed and prepared to achieve chemotherapy and enhance immunotherapy. Evodiamine (EVO) demonstrates chemotherapeutic efficacy and enhanced CD8+ T cell infiltration within the TME. Additionally, laser irradiation of Pyropheophorbide-a (Ppa) generates singlet oxygen, promoting tumor cell apoptosis and inducing immunogenic cell death (ICD). In vitro and in vivo experiments demonstrate that TEP exhibits significant cytotoxicity against 4T1 tumor cells and markedly inhibits tumor growth. Furthermore, TEP promotes the release of damage-associated molecular patterns (DAMPs) such as calreticulin (CRT), high mobility group box 1 protein (HMGB1), and adenosine triphosphate (ATP), which stimulates dendritic cells (DCs) maturation and activate adaptive immunity. Bilateral tumor experiments reveal that the combination therapy significantly increases the proportions of CD4+ and CD8+ T cells in tumors and central memory T cells (TCMs) in the spleen, demonstrating potent immunotherapy efficacy. In summary, TEP emerges as an innovative nano-drug with exceptional anti-tumor properties, offering a novel strategy for the treatment of TNBC.
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