免疫原性
复归
肿瘤微环境
肿瘤缺氧
癌症研究
免疫疗法
佐剂
广谱
免疫编辑
转移
免疫系统
光动力疗法
医学
癌症
肿瘤细胞
免疫学
生物
表型
化学
放射治疗
内科学
有机化学
基因
生物化学
组合化学
作者
Ao Chen,Fan Yang,Jing Kuang,Yuan Xiong,Bobin Mi,Ying Zhou,Jingjing Hu,Shujun Song,Tao Wan,Zhongzhong Wan,Hongyang Huang,Xinrun Li,Wen Song,Wen‐Xiu Qiu
标识
DOI:10.1021/acsami.1c15025
摘要
Immunotherapy is currently an important adjuvant therapy for malignant tumors besides surgical treatment. However, the heterogeneity and low immunogenicity of the tumor are two main challenges of the immunotherapy. Here, we have constructed a nanoplatform (CP@mRBC-PpIX) to realize reversion of the tumor acidosis and hypoxia through alkali and oxygen generation triggered by tumor acidosis. By targeting tumor universal features other than endogenous biomarkers, it was found that CP@mRBC-PpIX could polarize tumor-associated macrophages to anti-tumor M1 phenotype macrophages to enhance tumor immune response. Furthermore, under regional light irradiation, the reactive oxygen species produced by photosensitizers located in CP@mRBC-PpIX could increase the immunogenicity of tumors, so that tumor changes from an immunosuppressive "cold tumor" to an immunogenic "hot tumor," thereby increasing the infiltration and response of T cells, further amplifying the effect of immunotherapy. This strategy circumvented the problem of tumor heterogeneity to realize a kind of broad-spectrum immunotherapy, which could effectively prevent tumor metastasis and recurrence.
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