免疫检查点
免疫系统
表观遗传学
对偶(语法数字)
药品
药物输送
封锁
材料科学
医学
药理学
纳米技术
免疫学
生物
生物化学
受体
内科学
基因
文学类
艺术
作者
Huitong Ruan,Quanyin Hu,Di Wen,Qian Chen,Guojun Chen,Yifei Lü,Jinqiang Wang,Hao Cheng,Weiyue Lu,Zhen Gu
标识
DOI:10.1002/adma.201806957
摘要
Abstract Patients with advanced melanoma that is of low tumor‐associated antigen (TAA) expression often respond poorly to PD‐1/PD‐L1 blockade therapy. Epigenetic modulators, such as hypomethylation agents (HMAs), can enhance the antitumor immune response by inducing TAA expression. Here, a dual bioresponsive gel depot that can respond to the acidic pH and reactive oxygen species (ROS) within the tumor microenvironment (TME) for codelivery of anti‐PD1 antibody (aPD1) and Zebularine (Zeb), an HMA, is engineered. aPD1 is first loaded into pH‐sensitive calcium carbonate nanoparticles (CaCO 3 NPs), which are then encapsulated in the ROS‐responsive hydrogel together with Zeb (Zeb‐aPD1‐NPs‐Gel). It is demonstrated that this combination therapy increases the immunogenicity of cancer cells, and also plays roles in reversing immunosuppressive TME, which contributes to inhibiting the tumor growth and prolonging the survival time of B16F10‐melanoma‐bearing mice.
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