Ekdahl K N, Michaëlsson G, Gerdén B, Lööf L, Nilsson B
Department of Medical and Physiological Chemistry, Biomedical Centre, Uppsala, Sweden.
Arch Dermatol Res. 1995;287(3-4):225-30. doi: 10.1007/BF01105070.
The function of the fixed macrophage system in 18 psoriasis patients was evaluated by measuring the elimination rate of injected autologous erythrocytes coated with iC3b or IgG. The mean half-life of iC3b-coated erythrocytes was significantly prolonged in patients with psoriasis compared with healthy controls (4.7 +/- 0.8 vs 2.7 +/- 0.2 min, P = 0.01). There was also a decrease in the total number of cells eliminated from the circulation (2.5 +/- 0.2 x 10(8) vs 3.3 +/- 0.2 x 10(8), P = 0.01). There was an even more pronounced increase in the half-life of IgG-coated erythrocytes (85 +/- 18 vs 20 +/- 5 min, P < 0.001), with normal values in only 5 of 15 patients, and 4 of these 5 patients were receiving systemic treatment. The slow elimination was interpreted as being caused by primary or secondary defects in receptor function rather than by blocking of the receptors by immune complexes, since patients with psoriasis show normal levels of circulating immune complexes. Further studies are needed to elucidate the nature of these defects.
通过测量注射的包被iC3b或IgG的自体红细胞的清除率,评估了18例银屑病患者中固定巨噬细胞系统的功能。与健康对照相比,银屑病患者中包被iC3b的红细胞的平均半衰期显著延长(4.7±0.8对2.7±0.2分钟,P = 0.01)。循环中清除的细胞总数也有所减少(2.5±0.2×10⁸对3.3±0.2×10⁸,P = 0.01)。包被IgG的红细胞的半衰期增加更为明显(85±18对20±5分钟,P < 0.001),15例患者中只有5例正常,这5例患者中有4例正在接受全身治疗。清除缓慢被解释为是由受体功能的原发性或继发性缺陷引起的,而不是由免疫复合物对受体的阻断引起的,因为银屑病患者循环免疫复合物水平正常。需要进一步研究以阐明这些缺陷的性质。