Sanderson C J
National Institute for Medical Research, London, UK.
Int Arch Allergy Appl Immunol. 1991;94(1-4):122-6. doi: 10.1159/000235342.
Experiments in vitro have suggested that IL5 is a late-acting factor in eosinophil production, and that other factors such as IL3, G-CSF and GM-CSF are required for the production of committed eosinophil progenitors. Furthermore, work in vitro indicates that in addition to IL5, both IL3 and GM-CSF are capable of stimulating eosinophil differentiation. Thus, there would appear to be both considerable redundancy in cytokine actions in eosinophilia as well as a complex network of cytokine activities to induce eosinophilia. Experiments in vivo, however, suggest a less complicated control mechanism, dominated by IL5.
体外实验表明,白细胞介素5是嗜酸性粒细胞生成中的一种晚期作用因子,而生成定向嗜酸性粒细胞祖细胞则需要白细胞介素3、粒细胞集落刺激因子和粒细胞-巨噬细胞集落刺激因子等其他因子。此外,体外研究表明,除白细胞介素5外,白细胞介素3和粒细胞-巨噬细胞集落刺激因子均能够刺激嗜酸性粒细胞分化。因此,嗜酸性粒细胞增多症中细胞因子作用似乎存在相当大的冗余,同时也存在诱导嗜酸性粒细胞增多的复杂细胞因子活性网络。然而,体内实验表明,其控制机制没那么复杂,主要由白细胞介素5主导。