Cornish Ann L, Campbell Ian K, McKenzie Brent S, Chatfield Simon, Wicks Ian P
Autoimmunity and Transplantation Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Vic, Australia.
Nat Rev Rheumatol. 2009 Oct;5(10):554-9. doi: 10.1038/nrrheum.2009.178.
Granulocyte colony-stimulating factor (G-CSF) and granulocyte-macrophage colony-stimulating factor (GM-CSF) are well-recognized regulators of hematopoiesis and have an established role as growth factors in clinical practice. G-CSF and GM-CSF regulate myeloid cell production, differentiation and activation, and might also be important for driving inflammatory responses. Inappropriate engagement of this pathway could be a critical amplification mechanism when maladaptive immune responses predispose to autoimmunity and sterile tissue inflammation. We postulate that antagonism of G-CSF or GM-CSF could represent a novel therapeutic approach for a variety of autoimmune-mediated inflammatory diseases, including rheumatoid arthritis.
粒细胞集落刺激因子(G-CSF)和粒细胞-巨噬细胞集落刺激因子(GM-CSF)是公认的造血调节因子,在临床实践中作为生长因子发挥着既定作用。G-CSF和GM-CSF调节髓系细胞的产生、分化和激活,并且可能对驱动炎症反应也很重要。当适应不良的免疫反应易引发自身免疫和无菌性组织炎症时,该信号通路的不适当激活可能是一种关键的放大机制。我们推测,拮抗G-CSF或GM-CSF可能代表一种针对包括类风湿关节炎在内的多种自身免疫介导的炎症性疾病的新型治疗方法。