Faure M, Thivolet J, Gaucherand M
Arch Dermatol Res. 1980;269(3):275-80. doi: 10.1007/BF00406421.
The effects of thalidomide on chemotaxis of normal human peripheral blood PMN leukocytes have been studied in vitro. The chemotaxis factor was generated by interacting normal human serum with bovine gamma globulin-antibovine-gamma globulin immune complexes. At concentrations of 1, 10, and 100 microgram/ml, thalidomide failed to inhibit the chemotactic factor. At the same concentrations, erythromycin caused a marked inhibition of chemotaxis. Pre-incubation of PMNs with thalidomide or erythromycin caused a marked, dose-independent inhibition of chemotaxis. Random mobility did not appear to be affected. Inhibition of PMN chemotactic ability by thalidomide may account for its ability to improve inflammatory dermatoses, such as aphthosis.
已在体外研究了沙利度胺对正常人外周血中性粒细胞趋化性的影响。趋化因子是通过正常人血清与牛γ球蛋白 - 抗牛γ球蛋白免疫复合物相互作用产生的。在浓度为1、10和100微克/毫升时,沙利度胺未能抑制趋化因子。在相同浓度下,红霉素对趋化性有显著抑制作用。中性粒细胞与沙利度胺或红霉素预孵育会导致趋化性显著的、剂量非依赖性抑制。随机移动性似乎未受影响。沙利度胺对中性粒细胞趋化能力的抑制可能解释了其改善炎性皮肤病(如口疮病)的能力。