On the Biology and Therapeutic Modulation of Macrophages and Dendritic Cells in Cancer

被引:10
|
作者
Park, Matthew D. [1 ,2 ]
Belabed, Meriem [1 ,2 ]
Chen, Steven T. [1 ,2 ]
Hamon, Pauline [1 ,2 ]
Hegde, Samarth [1 ,2 ]
Mattiuz, Raphael [1 ,2 ]
Marron, Thomas U. [1 ,2 ,3 ,4 ]
Merad, Miriam [1 ,2 ,3 ,4 ]
机构
[1] Icahn Sch Med Mt Sinai, Marc & Jennifer Lipschultz Precis Immunol Inst, Tisch Canc Inst, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Dept Ontol Sci, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Div Hematol Oncol, Ctr Thorac Oncol, New York, NY 10029 USA
[4] Icahn Sch Med Mt Sinai, Early Phase Trials Unit, New York, NY 10029 USA
来源
关键词
cancer; mononuclear phagocyte; macrophage; dendritic cell; microenvironment; therapeutics; REGULATORY T-CELLS; CLONAL HEMATOPOIESIS; TISSUE-RESIDENT; STEADY-STATE; PROMOTES; ACTIVATION; IMMUNITY; METASTASIS; MONOCYTES; INFECTION;
D O I
10.1146/annurev-cancerbio-061521-085949
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Myeloid cells represent a dominant cellular compartment of tumor lesions and play key roles in tumor inception, progression, metastasis, and response to treatment. Mononuclear phagocytes (MNPs), which include dendritic cells and macrophages, are unique among myeloid cells, as they not only shape both the broader composition and state of the tumor microenvironment but can also specifically instruct cancer-specific, T cell-mediated tumor cell killing, making them especially attractive targets for cancer treatment. Although MNPs remain difficult to modulate therapeutically, our understanding of MNP biology in the antitumor immune response has expanded significantly, offering hope for new possibilities in cancer immunotherapy. Here, we review the recent advances in our study of the cellular identity, molecular diversity, and spatial organization of MNPs in tumors, and we discuss the importance of tailoring therapeutic strategies to incorporate these new insights into cancer treatment design.
引用
收藏
页码:291 / 311
页数:21
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