Hamilton John A
Arthritis and Inflammation Research Centre and Cooperative Research Centre for Chronic Inflammatory Diseases, University of Melbourne, Department of Medicine, The Royal Melbourne Hospital, Parkville, Victoria 3050, Australia.
Nat Rev Immunol. 2008 Jul;8(7):533-44. doi: 10.1038/nri2356.
Although they were originally defined as haematopoietic-cell growth factors, colony-stimulating factors (CSFs) have been shown to have additional functions by acting directly on mature myeloid cells. Recent data from animal models indicate that the depletion of CSFs has therapeutic benefit in many inflammatory and/or autoimmune conditions and as a result, early-phase clinical trials targeting granulocyte/macrophage colony-stimulating factor and macrophage colony-stimulating factor have now commenced. The distinct biological features of CSFs offer opportunities for specific targeting, but with some associated risks. Here, I describe these biological features, discuss the probable specific outcomes of targeting CSFs in vivo and highlight outstanding questions that need to be addressed.
尽管集落刺激因子(CSFs)最初被定义为造血细胞生长因子,但现已表明它们可通过直接作用于成熟髓样细胞而具有其他功能。来自动物模型的最新数据表明,在许多炎症和/或自身免疫性疾病中,CSFs的缺失具有治疗益处,因此,针对粒细胞/巨噬细胞集落刺激因子和巨噬细胞集落刺激因子的早期临床试验现已开始。CSFs独特的生物学特性为特异性靶向提供了机会,但也存在一些相关风险。在此,我描述这些生物学特性,讨论在体内靶向CSFs可能产生的具体结果,并强调需要解决的突出问题。