Hollán S R, Füst G, Mód A, Puskás E
Haematologia (Budap). 1980;13(1-4):263-82.
Longitudinal studies for the detection of circulating immune complexes (CIC-s) were performed in leukaemic patients using three methods in parallel. Results of these studies indicated that immune complexes in leukaemia are heterogeneous and their composition changes in the course of the disease. These results were supported by the changes in the concentration of a complement component (C1) and in the IgG subclasses in the immune complex-enriched fraction prepared by polyethylene glycol precipitation from different serum samples of individual patients with leukaemia. CIC-s from leukaemic patients are normally engulfed by granulocytes of healthy donors. The phagocytic capacity of leukaemic blast cells is hampered. The phagocytic activity through Fc and C3 receptors of peripheral mononuclear cells of leukaemic patients did not run parallel. On the basis of these studies it may be surmised that the total phagocytic capacity of the leukaemic patients cannot keep pace with the increased rate of immune complex formation.
采用三种方法并行,对白血病患者进行了纵向研究,以检测循环免疫复合物(CIC-s)。这些研究结果表明,白血病中的免疫复合物具有异质性,且其组成在疾病过程中会发生变化。这些结果得到了补体成分(C1)浓度以及通过聚乙二醇沉淀从个别白血病患者不同血清样本制备的富含免疫复合物部分中IgG亚类变化的支持。白血病患者的CIC-s通常会被健康供体的粒细胞吞噬。白血病原始细胞的吞噬能力受到阻碍。白血病患者外周单核细胞通过Fc和C3受体的吞噬活性并不平行。基于这些研究,可以推测白血病患者的总吞噬能力无法跟上免疫复合物形成增加的速度。