Colony stimulating factors and myeloid cell biology in health and disease

被引:232
作者
Hamilton, John A. [1 ]
Achuthan, Adrian [1 ]
机构
[1] Univ Melbourne, Royal Melbourne Hosp, Dept Med, Arthrit & Inflammat Res Ctr, Parkville, Vic 3050, Australia
关键词
COLLAGEN-INDUCED ARTHRITIS; TYROSINE KINASE INHIBITOR; HOUSE-DUST MITE; GM-CSF; DENDRITIC-CELL; FACTOR-I; RHEUMATOID-ARTHRITIS; T-CELLS; MACROPHAGE HETEROGENEITY; NEUTROPHIL PRODUCTION;
D O I
10.1016/j.it.2012.08.006
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 colony stimulating factors (CSFs), granulocyte macrophage-CSF (GM-CSF), macrophage-CSF (M-CSF or CSF-1) and granulocyte-CSF (G-CSF) were first identified as in vitro hematopoietic growth factors. They have since been shown to regulate myeloid cell numbers and function at steady state and during inflammation. Preclinical data suggest that targeting CSFs might be beneficial in autoimmune and inflammatory disease, and manipulation of CSF biology is now being tested in clinical trials. Here, we examine recent insights into CSF function, at steady state and during pathology, as provided by CSF or CSF receptor neutralization/deletion studies or from CSF administration. We discuss controversies regarding the role of CSFs in controlling specific myeloid cell populations and highlight how the newly identified M-CSF receptor ligand, interleukin (IL)-34, is necessitating a reassessment of the field.
引用
收藏
页码:81 / 89
页数:9
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