Harnessing and Enhancing Macrophage Phagocytosis for Cancer Therapy

被引:68
|
作者
Chen, Siqi [1 ]
Lai, Seigmund W. T. [1 ]
Brown, Christine E. [1 ,2 ]
Feng, Mingye [1 ]
机构
[1] City Hope Comprehens Canc Ctr, Beckman Res Inst, Dept Immunooncol, Duarte, CA 91010 USA
[2] City Hope Natl Med Ctr, Dept Hematol & Hematopoiet Cell Transplantat, 1500 E Duarte Rd, Duarte, CA 91010 USA
来源
FRONTIERS IN IMMUNOLOGY | 2021年 / 12卷
基金
美国国家卫生研究院;
关键词
macrophage; cancer immunotherapy; phagocytosis; antibody; chimeric antigen receptor (CAR); nanoparticle; TUMOR-ASSOCIATED MACROPHAGES; CAR-T-CELLS; IMMUNE CHECKPOINT INHIBITOR; ANTI-CD47; ANTIBODY; NANOPARTICLES; POLARIZATION; ACTIVATION; MECHANISMS; CD47; FC;
D O I
10.3389/fimmu.2021.635173
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cancer immunotherapy has revolutionized the paradigm for the clinical management of cancer. While FDA-approved cancer immunotherapies thus far mainly exploit the adaptive immunity for therapeutic efficacy, there is a growing appreciation for the importance of innate immunity in tumor cell surveillance and eradication. The past decade has witnessed macrophages being thrust into the spotlight as critical effectors of an innate anti-tumor response. Promising evidence from preclinical and clinical studies have established targeting macrophage phagocytosis as an effective therapeutic strategy, either alone or in combination with other therapeutic moieties. Here, we review the recent translational advances in harnessing macrophage phagocytosis as a pivotal therapeutic effort in cancer treatment. In addition, this review emphasizes phagocytosis checkpoint blockade and the use of nanoparticles as effective strategies to potentiate macrophages for phagocytosis. We also highlight chimeric antigen receptor macrophages as a next-generation therapeutic modality linking the closely intertwined innate and adaptive immunity to induce efficacious anti-tumor immune responses.
引用
收藏
页数:16
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