封锁
免疫系统
免疫疗法
癌症免疫疗法
胶质瘤
肿瘤微环境
癌症研究
免疫检查点
癌细胞
癌症
生物
免疫学
医学
受体
内科学
作者
Qi Chen,Yuyi Zheng,Xiaojie Chen,Yuan Xing,Jiajie Zhang,Xinyi Yan,Qi Zhang,Di Wu,Zhong Chen
标识
DOI:10.1002/advs.202308124
摘要
Abstract Cancer immunotherapy is an attractive strategy because it stimulates immune cells to target malignant cells by regulating the intrinsic activity of the immune system. However, due to lacking many immunologic markers, it remains difficult to treat glioma, a representative “cold” tumor. Herein, to wake the “hot” tumor immunity of glioma, Porphyromonas gingivalis (Pg) is customized with a coating to create an immunogenic tumor microenvironment and further prove the effect in combination with the immune checkpoint agent anti‐PD‐1, exhibiting elevated therapeutic efficacy. This is accomplished not by enhancing the delivery of PD‐1 blockade to enhance the effect of immunotherapy, but by introducing bacterial photothermal therapy to promote greater involvement of M1 cells in the immune response. After reaching glioma, the bacteria further target glioma cells and M2 phenotype macrophages selectively, enabling precise photothermal conversion for lysing tumor cells and M2 phenotype macrophages, which thereby enhances the positive feedback loop of cancer cells‐M1 macrophages‐T cells. Collectively, the bacteria synergized with PD‐1 blockade strategy may be the key to overcoming the immunosuppressive glioma microenvironment and improving the outcome of immunotherapy toward glioma.
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