肿瘤微环境
表型
癌症研究
免疫系统
溶瘤病毒
生物
肿瘤进展
免疫疗法
黑色素瘤
转移
免疫学
癌症
基因
遗传学
作者
Lina Liu,Qiang Li,Chen Chen,Wenjie Xin,Chao Han,Zichun Hua
出处
期刊:iScience
[Cell Press]
日期:2024-03-02
卷期号:27 (4): 109372-109372
被引量:5
标识
DOI:10.1016/j.isci.2024.109372
摘要
In the tumor microenvironment (TME), tumor-associated NEs (TANs) have the potential to be protumorigenic or antitumorigenic within the TME in response to environmental cues. The diversity and plasticity of NEs (NEs) underlie the dual potential of TANs in the TME. Here, we utilized the tumor-targeting bacterium VNP20009 (VNP) to carry a plasmid expressed IFNβ (VNP-IFNβ), which can deliver IFNβ and remodel TANs to an antitumorigenic phenotype, and performed preclinical evaluations in the B16F10 lung metastasis model and the B16F10 subcutaneous xenograft model. Compared with VNP, VNP-IFNβ recruited more NEs and macrophages (Mφs) with antitumor phenotypes in lung metastases and activated dendritic cells (DCs) differentiation, which activated antitumor immune responses of CD4
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