Potential New Cancer Immunotherapy: Anti-CD47-SIRPα Antibodies

被引:18
作者
Lu, Quansheng [1 ]
Chen, Xi [1 ]
Wang, Shan [2 ]
Lu, Yu [1 ]
Yang, Chunsheng [3 ]
Jiang, Guan [1 ]
机构
[1] Xuzhou Med Univ, Affiliated Hosp, Dept Dermatol, Xuzhou 221002, Jiangsu, Peoples R China
[2] Xuzhou Med Univ, Dept Gastroenterol, Affiliated Hosp, Xuzhou 221002, Jiangsu, Peoples R China
[3] Xuzhou Med Univ, Peoples Hosp Huaian 2, Affiliated Huaian Hosp, Dept Dermatol, Huaian 223002, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2020年 / 13卷
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
immunotherapy; CD47; SIRP alpha; macrophage; tumor; TUMOR-ASSOCIATED MACROPHAGES; CD47; BLOCKADE; THERAPEUTIC TARGET; CELLS; PROGRESSION; INHIBITOR; SYSTEM; FUSION; SELF;
D O I
10.2147/OTT.S249822
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
CD47 belongs to immunoglobulin superfamily and is widely expressed on the surface of cell membrane, while another transmembrane protein SIRP alpha is restricted to the surface of macrophages, dendritic cells, and nerve cells. As a cell surface receptor and ligand, respectively, CD47 and SIRP alpha interact to regulate cell migration and phagocytic activity, and maintain immune homeostasis. In recent years, studies have found that immunoglobulin superfamily CD47 is overexpressed widely across tumor types, and CD47 plays an important role in suppressing phagocytes activity through binding to the transmembrane protein SIRP alpha in phagocytic cells. Therefore, targeting CD47 may be a novel strategy for cancer immunotherapy, and a variety of anti-CD47 antibodies have appeared, such as humanized 5F9 antibody, B6H12 antibody, ZF1 antibody, and so on. This review mainly describes the research history of CD47-SIRP alpha and focuses on macrophage-mediated CD47-SIRP alpha immunotherapy of tumors.
引用
收藏
页码:9323 / 9331
页数:9
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