Vicioso M A, Garaud J J, Réglier-Poupet H, Lebeaut A, Gougerot-Pocidalo M A, Chollet-Martin S
Immunology Laboratory and INSERM U. 479, X. Bichat University, Paris, France.
Eur Cytokine Netw. 1998 Sep;9(3):247-53.
Neutrophils and monocytes are the major classes of phagocytes that migrate from the blood stream and accumulate in inflamed tissues in response to various chemoattractants. Because IL-10 is a potent anti-inflammatory cytokine, we analyzed its in vitro effect on chemotaxis using an under agarose method. We found that, as compared to prednisolone, IL-10 alone was a modest inhibitor of C5a, fMLP and IL-8-induced neutrophil chemotaxis, and C5a-induced monocyte chemotaxis. However, GM-CSF pretreatment of the cells potentiated this inhibitory effect. Similarly, the IL-10 induced modulation of the beta2 integrin CD11b/CD18 adhesion molecule expression was only observed on GM-CSF-preactivated neutrophils and monocytes. Taken together, these results suggest that the migration and accumulation of phagocytes at infection sites would not be significantly affected by IL-10 given as an immunomodulatory therapy.
中性粒细胞和单核细胞是主要的吞噬细胞类型,它们从血流中迁移并响应各种趋化因子而在炎症组织中聚集。由于白细胞介素-10(IL-10)是一种强效的抗炎细胞因子,我们使用琼脂糖下层法分析了其对趋化作用的体外影响。我们发现,与泼尼松龙相比,单独的IL-10对C5a、fMLP和IL-8诱导的中性粒细胞趋化作用以及C5a诱导的单核细胞趋化作用是一种适度的抑制剂。然而,细胞的粒细胞-巨噬细胞集落刺激因子(GM-CSF)预处理增强了这种抑制作用。同样,仅在GM-CSF预激活的中性粒细胞和单核细胞上观察到IL-10诱导的β2整合素CD11b/CD18黏附分子表达的调节。综上所述,这些结果表明,作为免疫调节疗法给予的IL-10不会显著影响吞噬细胞在感染部位的迁移和聚集。