CD47型
生物
髓系细胞
髓样
免疫检查点
癌症研究
受体
细胞生物学
细胞毒性T细胞
免疫系统
调节器
免疫学
干细胞
免疫疗法
遗传学
基因
体外
作者
Meike E. W. Logtenberg,Ferenc A. Scheeren,Ton N. Schumacher
出处
期刊:Immunity
[Cell Press]
日期:2020-05-01
卷期号:52 (5): 742-752
被引量:365
标识
DOI:10.1016/j.immuni.2020.04.011
摘要
The cytotoxic activity of myeloid cells is regulated by a balance of signals that are transmitted through inhibitory and activating receptors. The Cluster of Differentiation 47 (CD47) protein, expressed on both healthy and cancer cells, plays a pivotal role in this balance by delivering a “don’t eat me signal” upon binding to the Signal-regulatory protein alpha (SIRPα) receptor on myeloid cells. Here, we review the current understanding of the role of the CD47-SIRPα axis in physiological tissue homeostasis and as a promising therapeutic target in, among others, oncology, fibrotic diseases, atherosclerosis, and stem cell therapies. We discuss gaps in understanding and highlight where additional insight will be beneficial to allow optimal exploitation of this myeloid cell checkpoint as a target in human disease.
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