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
相关论文
共 182 条
  • [1] Diversification of human plasmacytoid predendritic cells in response to a single stimulus
    Alculumbre, Solana G.
    Saint-Andre, Violaine
    Di Domizio, Jeremy
    Vargas, Pablo
    Sirven, Philemon
    Bost, Pierre
    Maurin, Mathieu
    Maiuri, Paolo
    Wery, Maxime
    San Roman, Mabel
    Savey, Lea
    Touzot, Maxime
    Terrier, Benjamin
    Saadoun, David
    Conrad, Curdin
    Gilliet, Michel
    Morillon, Antonin
    Soumelis, Vassili
    [J]. NATURE IMMUNOLOGY, 2018, 19 (01) : 63 - +
  • [2] The ectonucleotidases CD39 and CD73: Novel checkpoint inhibitor targets
    Allard, Bertrand
    Longhi, Maria Serena
    Robson, Simon C.
    Stagg, John
    [J]. IMMUNOLOGICAL REVIEWS, 2017, 276 (01) : 121 - 144
  • [3] LAG3 (CD223) as a cancer immunotherapy target
    Andrews, Lawrence P.
    Marciscano, Ariel E.
    Drake, Charles G.
    Vignali, Dario A. A.
    [J]. IMMUNOLOGICAL REVIEWS, 2017, 276 (01) : 80 - 96
  • [4] Type I Interferons Induce Apoptosis by Balancing cFLIP and Caspase-8 Independent of Death Ligands
    Apelbaum, Amir
    Yarden, Ganit
    Warszawski, Shira
    Harari, Daniel
    Schreiber, Gideon
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2013, 33 (04) : 800 - 814
  • [5] Deciphering cell-cell interactions and communication from gene expression
    Armingol, Erick
    Officer, Adam
    Harismendy, Olivier
    Lewis, Nathan E.
    [J]. NATURE REVIEWS GENETICS, 2021, 22 (02) : 71 - 88
  • [6] Biological Consequences of MHC-II Expression by Tumor Cells in Cancer
    Axelrod, Margaret L.
    Cook, Rebecca S.
    Johnson, Douglas B.
    Balko, Justin M.
    [J]. CLINICAL CANCER RESEARCH, 2019, 25 (08) : 2392 - 2402
  • [7] Interferon-α Suppresses cAMP to Disarm Human Regulatory T Cells
    Bacher, Nicole
    Raker, Verena
    Hofmann, Claudia
    Graulich, Edith
    Schwenk, Melanie
    Baumgrass, Ria
    Bopp, Tobias
    Zechner, Ulrich
    Merten, Luzie
    Becker, Christian
    Steinbrink, Kerstin
    [J]. CANCER RESEARCH, 2013, 73 (18) : 5647 - 5656
  • [8] Prognostic impact of high levels of circulating plasmacytoid dendritic cells in breast cancer
    Bailur, Jithendra Kini
    Gueckel, Brigitte
    Pawelec, Graham
    [J]. JOURNAL OF TRANSLATIONAL MEDICINE, 2016, 14
  • [9] TNF-α in promotion and progression of cancer
    Balkwill, Frances
    [J]. CANCER AND METASTASIS REVIEWS, 2006, 25 (03) : 409 - 416
  • [10] NKT cell subsets as key participants in liver physiology and pathology
    Bandyopadhyay, Keya
    Marrero, Idania
    Kumar, Vipin
    [J]. CELLULAR & MOLECULAR IMMUNOLOGY, 2016, 13 (03) : 337 - 346