Emerging roles of plasmacytoid dendritic cell crosstalk in tumor immunity

被引:4
作者
Yang, Leilei [1 ,2 ]
Li, Songya [2 ]
Chen, Liuhui [2 ]
Zhang, Yi [1 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Biotherapy Ctr, Zhengzhou 450052, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Dept Stomatol, Zhengzhou 450052, Peoples R China
基金
中国国家自然科学基金;
关键词
Plasmacytoid dendritic cell; tumor microenvironment; cell crosstalk; immune activation; immune suppression; IFN-ALPHA SECRETION; EPSTEIN-BARR-VIRUS; INTERFERON-PRODUCING CELLS; TRANSCRIPTION FACTOR E2-2; I INTERFERON; PROSTAGLANDIN E-2; CXCR3; LIGANDS; LYMPH-NODES; T-CELLS; B-CELLS;
D O I
10.20892/j.issn.2095-3941.2023.0241
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Plasmacytoid dendritic cells (pDCs) are a pioneer cell type that produces type I interferon (IFN-I) and promotes antiviral immune responses. However, they are tolerogenic and, when recruited to the tumor microenvironment (TME), play complex roles that have long been a research focus. The interactions between pDCs and other components of the TME, whether direct or indirect, can either promote or hinder tumor development; consequently, pDCs are an intriguing target for therapeutic intervention. This review provides a comprehensive overview of pDC crosstalk in the TME, including crosstalk with various cell types, biochemical factors, and microorganisms. An in-depth understanding of pDC crosstalk in TME should facilitate the development of novel pDC-based therapeutic methods.
引用
收藏
页码:728 / 747
页数:20
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