奥沙利铂
免疫疗法
癌症研究
前药
免疫原性细胞死亡
免疫系统
医学
癌症免疫疗法
药品
结直肠癌
癌症
药理学
材料科学
免疫学
内科学
作者
Qingfei Zhang,Gaizhen Kuang,Yunru Yu,Xiaoya Ding,Haozhen Ren,Weijian Sun,Yuanjin Zhao
标识
DOI:10.1021/acsami.2c16564
摘要
and retained locally to reduce systemic toxicity. After being endocytosed by cancer cells, the cytotoxic oxaliplatin and NLG919 could be successfully triggered to release from DDP NPs in a chain-shattering manner, leading to the immunogenic cell death (ICD) of tumor cells and the suppression of intratumoral immunosuppressive Tregs, respectively. With the assistance of an immune modulator, the chemotherapeutics-induced ICD could trigger robust systemic antitumor immune responses, presenting superior synergistic antitumor efficacies. Thus, the hierarchical microparticles could substantially inhibit the growth of mouse subcutaneous colorectal tumors, breast tumors, and colorectal tumors with large initial sizes via synergized chemo-immunotherapy, showing great potential in the practical clinical application of oncotherapy.
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