Targeting GM-CSF in inflammatory diseases

被引:241
作者
Wicks, Ian P. [1 ]
Roberts, Andrew W. [1 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Parkville, Vic 3052, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
COLONY-STIMULATING FACTOR; COLLAGEN-INDUCED ARTHRITIS; ALPHA MONOCLONAL-ANTIBODY; FACTOR-DEFICIENT MICE; B-CELLS PROTECT; RHEUMATOID-ARTHRITIS; DENDRITIC CELLS; MACROPHAGE DIFFERENTIATION; T-CELLS; TRANSGENIC EXPRESSION;
D O I
10.1038/nrrheum.2015.161
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Granulocyte-macrophage colony stimulating factor (GM-CSF) is a growth factor first identified as an inducer of differentiation and proliferation of granulocytes and macrophages derived from haematopoietic progenitor cells. Later studies have shown that GM-CSF is involved in a wide range of biological processes in both innate and adaptive immunity, with its production being tightly linked to the response to danger signals. Given that the functions of GM-CSF span multiple tissues and biological processes, this cytokine has shown potential as a new and important therapeutic target in several autoimmune and inflammatory disorders-particularly in rheumatoid arthritis. Indeed, GM-CSF was one of the first cytokines detected in human synovial fluid from inflamed joints. Therapies that target GM-CSF or its receptor have been tested in preclinical studies with promising results, further supporting the potential of targeting the GM-CSF pathway. In this Review, we discuss our expanding view of the biology of GM-CSF, outline what has been learnt about GM-CSF from studies of animal models and human diseases, and summarize the results of early phase clinical trials evaluating GM-CSF antagonism in inflammatory disorders.
引用
收藏
页码:37 / 48
页数:12
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