Tumor-Associated Macrophages: From Mechanisms to Therapy

被引:3867
作者
Noy, Roy [1 ]
Pollard, Jeffrey W. [1 ,2 ]
机构
[1] Albert Einstein Coll Med, Ctr Study Reprod Biol & Womens Hlth, Dept Dev & Mol Biol, New York, NY 10461 USA
[2] Univ Edinburgh, Queens Med Res Inst, Ctr Reprod Hlth, MRC, Edinburgh EH16 4TJ, Midlothian, Scotland
基金
英国惠康基金;
关键词
REGULATORY T-CELLS; MYELOID CELLS; SUPPRESSOR-CELLS; DENDRITIC CELLS; MICROENVIRONMENTAL REGULATION; COSTIMULATORY MOLECULES; ALTERNATIVE ACTIVATION; CLINICAL-SIGNIFICANCE; PULMONARY METASTASIS; MAMMARY CARCINOMAS;
D O I
10.1016/j.immuni.2014.06.010
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
The tumor microenvironment is a complex ecology of cells that evolves with and provides support to tumor cells during the transition to malignancy. Among the innate and adaptive immune cells recruited to the tumor site, macrophages are particularly abundant and are present at all stages of tumor progression. Clinical studies and experimental mouse models indicate that these macrophages generally play a protumoral role. In the primary tumor, macrophages can stimulate angiogenesis and enhance tumor cell invasion, motility, and intravasation. During monocytes and/or metastasis, macrophages prime the premetastatic site and promote tumor cell extravasation, survival, and persistent growth. Macrophages are also immunosuppressive, preventing tumor cell attack by natural killer and T cells during tumor progression and after recovery from chemo-or immunotherapy. Therapeutic success in targeting these protumoral roles in preclinical models and in early clinical trials suggests that macrophages are attractive targets as part of combination therapy in cancer treatment.
引用
收藏
页码:49 / 61
页数:13
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