巨噬细胞集落刺激因子
巨噬细胞
生物
免疫学
炎症
癌症研究
集落刺激因子
免疫系统
髓样
造血
细胞生物学
干细胞
体外
生物化学
作者
David Hume,Kelli P. A. MacDonald
出处
期刊:Blood
[American Society of Hematology]
日期:2012-02-23
卷期号:119 (8): 1810-1820
被引量:564
标识
DOI:10.1182/blood-2011-09-379214
摘要
Abstract Macrophage-colony stimulating factor (CSF-1) signaling through its receptor (CSF-1R) promotes the differentiation of myeloid progenitors into heterogeneous populations of monocytes, macrophages, dendritic cells, and bone-resorbing osteoclasts. In the periphery, CSF-1 regulates the migration, proliferation, function, and survival of macrophages, which function at multiple levels within the innate and adaptive immune systems. Macrophage populations elicited by CSF-1 are associated with, and exacerbate, a broad spectrum of pathologies, including cancer, inflammation, and bone disease. Conversely, macrophages can also contribute to immunosuppression, disease resolution, and tissue repair. Recombinant CSF-1, antibodies against the ligand and the receptor, and specific inhibitors of CSF-1R kinase activity have been each been tested in a range of animal models and in some cases, in patients. This review examines the potential clinical uses of modulators of the CSF-1/CSF-1R system. We conclude that CSF-1 promotes a resident-type macrophage phenotype. As a treatment, CSF-1 has therapeutic potential in tissue repair. Conversely, inhibition of CSF-1R is unlikely to be effective in inflammatory disease but may have utility in cancer.
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