Camussi G, Bosio D, Segoloni G, Tetta C, Vercellone A
Ric Clin Lab. 1978 Jan-Jun;8(1-2):56-64.
Several findings reveal the involvement of the IgE-basophil-mastocyte-platelet-activating-factor (PAF) system in human acute post-streptococcal glomerulonephritis. In the acute phases of the disease there is a transient, marked reduction in the circulating metachromatically staining basophils, indicating an in vivo basophil degranulation. The blood reservoirs of PAF are depleted. The number of metachromatic mastocytes in renal biopsy samples was very low and morphological aspects of degranulation were present. In vitro, we demonstrated basophil degranulation and PAF release in presence of exogenous streptococcal Ags after recovery. These findings suggest that the IgE-basophil-mastocyte-PAF system may play a role in human pathology, as has been shown in immune complex (Ic) deposition in acute serum sickness in rabbits.
多项研究结果揭示了IgE-嗜碱性粒细胞-肥大细胞-血小板活化因子(PAF)系统在人类急性链球菌感染后肾小球肾炎中的作用。在疾病的急性期,循环中异染性染色的嗜碱性粒细胞出现短暂、显著减少,表明体内嗜碱性粒细胞发生脱颗粒。PAF的血库被耗尽。肾活检样本中异染性肥大细胞数量非常低,且存在脱颗粒的形态学表现。在体外,我们证实在恢复期外源性链球菌抗原存在的情况下嗜碱性粒细胞会发生脱颗粒并释放PAF。这些发现表明,IgE-嗜碱性粒细胞-肥大细胞-PAF系统可能在人类病理学中发挥作用,正如在兔急性血清病的免疫复合物(Ic)沉积中所显示的那样。