The complex role of tumor-infiltrating macrophages

被引:668
作者
Christofides, Anthos [1 ,2 ,3 ]
Strauss, Laura [1 ,2 ,3 ,5 ]
Yeo, Alan [3 ]
Cao, Carol [1 ,2 ,4 ]
Charest, Alain [2 ,3 ]
Boussiotis, Vassiliki A. [1 ,2 ,3 ]
机构
[1] Harvard Med Sch, Div Hematol Oncol, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA
[2] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA 02115 USA
[3] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Canc Ctr, Boston, MA 02115 USA
[4] Harvard Univ, Cambridge, MA USA
[5] Sanofi Tidal, Cambridge, MA USA
关键词
MYELOID CELLS; PATROLLING MONOCYTES; IMMUNE CHECKPOINT; PD-1; EXPRESSION; INFLAMMATION; ACTIVATION; METASTASIS; REVEALS; POLARIZATION; HOMEOSTASIS;
D O I
10.1038/s41590-022-01267-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Boussiotis and colleagues review the hallmarks of tumor-associated macrophages and discuss the mechanisms that contribute to their pathophysiological adaptations to the tumor microenvironment. Long recognized as an evolutionarily ancient cell type involved in tissue homeostasis and immune defense against pathogens, macrophages are being re-discovered as regulators of several diseases, including cancer. Tumor-associated macrophages (TAMs) represent the most abundant innate immune population in the tumor microenvironment (TME). Macrophages are professional phagocytic cells of the hematopoietic system specializing in the detection, phagocytosis and destruction of bacteria and other harmful micro-organisms, apoptotic cells and metabolic byproducts. In contrast to these healthy macrophage functions, TAMs support cancer cell growth and metastasis and mediate immunosuppressive effects on the adaptive immune cells of the TME. Cancer is one of the most potent insults on macrophage physiology, inducing changes that are intimately linked with disease progression. In this Review, we outline hallmarks of TAMs and discuss the emerging mechanisms that contribute to their pathophysiological adaptations and the vulnerabilities that provide attractive targets for therapeutic exploitation in cancer.
引用
收藏
页码:1148 / 1156
页数:9
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