Sturfelt G, Sjöholm A G, Truedsson L
Department of Rheumatology, University Hospital of Lund, Sweden.
Immunol Lett. 1989 Feb;20(3):231-6. doi: 10.1016/0165-2478(89)90085-0.
Factor D depleted serum did not support hemolysis of rabbit erythrocytes and solubilization of performed immune complexes. Fluid phase C3 cleavage increased in a dose dependent manner when D protein was added to normal or to factor D depleted serum. During short incubation factor D concentrations were correlated with the capacity of serum to solubilize immune complexes and to lyse rabbit erythrocytes. With prolonged incubation, the hemolytic activity decreased in a factor D dose dependent manner. This was probably due to fluid phase breakdown of C3 and factor B in the presence of high factor D concentrations. Hypocomplementemic sera from patients with active systemic lupus erythematosus (SLE) did not support solubilization of bovine serum albumin (BSA) anti-BSA complexes when factor D was added in excess. Patients with polycystic kidney disease with reduced renal function and high factor D concentrations showed increased concentrations of circulating C3d/dg fragments. The possibility was considered that high factor D concentrations in uremia might promote fluid phase C3 degradation and thereby limit the in vivo efficiency of alternative pathway activation on target surfaces.
缺乏因子D的血清不支持兔红细胞的溶血和已形成免疫复合物的溶解。当将D蛋白添加到正常血清或缺乏因子D的血清中时,液相C3裂解呈剂量依赖性增加。在短时间孵育期间,因子D浓度与血清溶解免疫复合物和裂解兔红细胞的能力相关。随着孵育时间延长,溶血活性以因子D剂量依赖性方式降低。这可能是由于在高因子D浓度存在下C3和因子B的液相降解。当过量添加因子D时,活动性系统性红斑狼疮(SLE)患者的低补体血症血清不支持牛血清白蛋白(BSA)抗BSA复合物的溶解。肾功能降低且因子D浓度高的多囊肾病患者循环C3d/dg片段浓度增加。有人认为,尿毒症中高因子D浓度可能促进液相C3降解,从而限制替代途径在靶表面激活的体内效率。