Impaired function of dendritic cells within the tumor microenvironment

被引:39
作者
Xiao, Zhihua [1 ,2 ]
Wang, Ruiqi [1 ]
Wang, Xuyan [1 ]
Yang, Haikui [1 ]
Dong, Jiamei [1 ]
He, Xin [1 ]
Yang, Yang [1 ]
Guo, Jiahao [1 ,2 ]
Cui, Jiawen [1 ,2 ]
Zhou, Zhiling [1 ]
机构
[1] Jinan Univ, Zhuhai Peoples Hosp, Dept Pharm, Zhuhai Hosp, Zhuhai, Peoples R China
[2] Jinan Univ, Coll Pharm, Guangzhou, Peoples R China
关键词
dendritic cell; tumor microenvironment; immune tolerance; immunosuppressive populations; DC-based vaccine; REGULATORY T-CELLS; CROSS-PRESENTATION; IMMUNE CELLS; CANCER; HYPOXIA; ANTIGEN; MACROPHAGES; INCREASES; ACTIVATION; MECHANISMS;
D O I
10.3389/fimmu.2023.1213629
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dendritic cells (DCs), a class of professional antigen-presenting cells, are considered key factors in the initiation and maintenance of anti-tumor immunity due to their powerful ability to present antigen and stimulate T-cell responses. The important role of DCs in controlling tumor growth and mediating potent anti-tumor immunity has been demonstrated in various cancer models. Accordingly, the infiltration of stimulatory DCs positively correlates with the prognosis and response to immunotherapy in a variety of solid tumors. However, accumulating evidence indicates that DCs exhibit a significantly dysfunctional state, ultimately leading to an impaired anti-tumor immune response due to the effects of the immunosuppressive tumor microenvironment (TME). Currently, numerous preclinical and clinical studies are exploring immunotherapeutic strategies to better control tumors by restoring or enhancing the activity of DCs in tumors, such as the popular DC-based vaccines. In this review, an overview of the role of DCs in controlling tumor progression is provided, followed by a summary of the current advances in understanding the mechanisms by which the TME affects the normal function of DCs, and concluding with a brief discussion of current strategies for DC-based tumor immunotherapy.
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页数:13
相关论文
共 174 条
[1]  
Anderson NM, 2020, CURR BIOL, V30, pR921, DOI 10.1016/j.cub.2020.06.081
[2]   Intratumoral combination therapy with poly(I:C) and resiquimod synergistically triggers tumor-associated macrophages for effective systemic antitumoral immunity [J].
Anfray, Clement ;
Mainini, Francesco ;
Digifico, Elisabeth ;
Maeda, Akihiro ;
Sironi, Marina ;
Erreni, Marco ;
Anselmo, Achille ;
Ummarino, Aldo ;
Gandoy, Sara ;
Exposito, Francisco ;
Redrado, Miriam ;
Serrano, Diego ;
Calvo, Alfonso ;
Martens, Marvin ;
Bravo, Susana ;
Mantovani, Alberto ;
Allavena, Paola ;
Andon, Fernando Torres .
JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2021, 9 (09)
[3]   Foxp3 Reprograms T Cell Metabolism to Function in Low-Glucose, High-Lactate Environments [J].
Angelin, Alessia ;
Gil-de-Gomez, Luis ;
Dahiya, Satinder ;
Jiao, Jing ;
Guo, Lili ;
Levine, Matthew H. ;
Wang, Zhonglin ;
Quinn, William J., III ;
Kopinski, Piotr K. ;
Wang, Liqing ;
Akimova, Tatiana ;
Liu, Yujie ;
Bhatti, Tricia R. ;
Han, Rongxiang ;
Laskin, Benjamin L. ;
Baur, Joseph A. ;
Blair, Ian A. ;
Wallace, Douglas C. ;
Hancock, Wayne W. ;
Beier, Ulf H. .
CELL METABOLISM, 2017, 25 (06) :1282-+
[4]  
[Anonymous], 2023, NCCN clinical practice guidelines in oncology: Survivorship
[5]   Tumor-associated fibroblasts predominantly come from local and not circulating precursors [J].
Arina, Ainhoa ;
Idel, Christian ;
Hyjek, Elizabeth M. ;
Alegre, Maria-Luisa ;
Wang, Ying ;
Bindokas, Vytautas P. ;
Weichselbaum, Ralph R. ;
Schreiber, Hans .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 113 (27) :7551-7556
[6]   A natural killer-dendritic cell axis defines checkpoint therapy-responsive tumor microenvironments [J].
Barry, Kevin C. ;
Hsu, Joy ;
Broz, Miranda L. ;
Cueto, Francisco J. ;
Binnewies, Mikhail ;
Combes, Alexis J. ;
Nelson, Amanda E. ;
Loo, Kimberly ;
Kumar, Raj ;
Rosenblum, Michael D. ;
Alvarado, Michael D. ;
Wolf, Denise M. ;
Bogunovic, Dusan ;
Bhardwaj, Nina ;
Daud, Adil, I ;
Ha, Patrick K. ;
Ryan, William R. ;
Pollack, Joshua L. ;
Samad, Bushra ;
Asthana, Saurabh ;
Chan, Vincent ;
Krummel, Matthew F. .
NATURE MEDICINE, 2018, 24 (08) :1178-1191
[7]   RETRACTED: Dual Blockade of PD-1 and LAG3 Immune Checkpoints Increases Dendritic Cell Vaccine Mediated T Cell Responses in Breast Cancer Model (Retracted Article) [J].
Barshidi, Asal ;
Karpisheh, Vahid ;
Noukabadi, Fatemeh Karimian ;
Kiani, Fariba Karoon ;
Mohammadi, Mohammad ;
Afsharimanesh, Negin ;
Ebrahimi, Farbod ;
Kiaie, Seyed Hossein ;
Navashenaq, Jamshid Gholizadeh ;
Hojjat-Farsangi, Mohammad ;
Zolbanin, Naime Majidi ;
Mahmoodpoor, Ata ;
Hassannia, Hadi ;
Nami, Sanam ;
Jalali, Pooya ;
Jafari, Reza ;
Jadidi-Niaragh, Farhad .
PHARMACEUTICAL RESEARCH, 2022, 39 (08) :1851-1866
[8]   A single-cell map of intratumoral changes during anti-PD1 treatment of patients with breast cancer [J].
Bassez, Ayse ;
Vos, Hanne ;
Van Dyck, Laurien ;
Floris, Giuseppe ;
Arijs, Ingrid ;
Desmedt, Christine ;
Boeckx, Bram ;
Vanden Bempt, Marlies ;
Nevelsteen, Ines ;
Lambein, Kathleen ;
Punie, Kevin ;
Neven, Patrick ;
Garg, Abhishek D. ;
Wildiers, Hans ;
Qian, Junbin ;
Smeets, Ann ;
Lambrechts, Diether .
NATURE MEDICINE, 2021, 27 (05) :820-+
[9]   Ionizing Radiation Curtails Immunosuppressive Effects From Cancer-Associated Fibroblasts on Dendritic Cells [J].
Berzaghi, Rodrigo ;
Tornaas, Stian ;
Lode, Kristin ;
Hellevik, Turid ;
Martinez-Zubiaurre, Inigo .
FRONTIERS IN IMMUNOLOGY, 2021, 12
[10]   Cross-talk among myeloid-derived suppressor cells, macrophages, and tumor cells impacts the inflammatory milieu of solid tumors [J].
Beury, Daniel W. ;
Parker, Katherine H. ;
Nyandjo, Maeva ;
Sinha, Pratima ;
Carter, Kayla A. ;
Ostrand-Rosenberg, Suzanne .
JOURNAL OF LEUKOCYTE BIOLOGY, 2014, 96 (06) :1109-1118