Targeting Tumor-Associated Macrophages as a Potential Strategy to Enhance the Response to Immune Checkpoint Inhibitors

被引:185
作者
Cassetta, Luca [1 ]
Kitamura, Takanori [1 ,2 ,3 ]
机构
[1] Queens Med Res Inst, Med Res Council, Ctr Reprod Hlth, Edinburgh, Midlothian, Scotland
[2] Univ Edinburgh, Royal Dick Sch Vet Studies, Edinburgh, Midlothian, Scotland
[3] Univ Edinburgh, Roslin Inst, Edinburgh, Midlothian, Scotland
基金
欧盟地平线“2020”; 英国惠康基金; 美国国家卫生研究院;
关键词
tumor microenvironment; immunotherapy; checkpoint inhibitor; CD8(+) T cell; macrophage; TAM; tumor immunology; CANCER; CELLS; POLARIZATION; METAANALYSIS; PROGRESSION; RESISTANCE; EFFICACY; THERAPY; PD-L1;
D O I
10.3389/fcell.2018.00038
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Inhibition of immune checkpoint pathways in CD8(+) T cell is a promising therapeutic strategy for the treatment of solid tumors that has shown significant anti-tumor effects and is now approved by the FDA to treat patients with melanoma and lung cancer. However the response to this therapy is limited to a certain fraction of patients and tumor types, for reasons still unknown. To ensure success of this treatment, CD8(+) T cells, the main target of the checkpoint inhibitors, should exert full cytotoxicity against tumor cells. However recent studies show that tumor-associated macrophages (TAM) can impede this process by different mechanisms. In this mini-review we will summarize recent studies showing the effect of TAM targeting on immune checkpoint inhibitors efficacy. We will also discuss on the limitations of the current strategies as well on the future scientific challenges for the progress of the tumor immunology field.
引用
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页数:6
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