Schena P F, Pastore A, Sinico R A, Montinaro V, Fornasieri A
Chair of Medical Therapy, University of Bari, Italy.
J Immunol. 1988 Jul 1;141(1):125-30.
Primary IgA nephropathy (IgAN) is characterized by the presence of immune complexes (IC), high levels of polymeric IgA (pIgA), and IgA rheumatoid factor (RF) in the blood. The impaired capacity of serum to solubilize IC in the presence of normal values of C hemolytic activity as well as high serum levels of C3, C4, and properdin factor B have led us to analyze whether pIgA and IgA RF from patients with IgAN where capable of inhibiting the capacity of normal human serum to solubilize immune precipitates (BSA-anti-BSA) preformed at equivalence. The results showed a significant reduced mean capacity of serum from patients with IgAN to solubilize "in vitro" immune precipitates (p less than 0.001) and significant high mean levels of pIgA (p less than 0.001) and IgA RF (p less than 0.005) in the blood. Increasing amounts of pIgA inhibited solubilization of IC in the fluid phase, and inhibitory activity was also shown by the IgA RF. There were inverse correlations between pIgA and the capacity of serum to solubilize IC (r = -0.36; p less than 0.05), and between IgA RF and the complement-mediated solubilization (r = -0.57; p less than 0.001). It is suggested that pIgA and IgA RF may be responsible for the impaired complement-mediated solubilization of serum and the persistence of insoluble nephritogenic IC in the blood of patients with primary IgAN.
原发性IgA肾病(IgAN)的特征是血液中存在免疫复合物(IC)、高水平的聚合IgA(pIgA)和IgA类风湿因子(RF)。在C溶血活性正常以及血清C3、C4和备解素因子B水平较高的情况下,血清溶解IC的能力受损,这促使我们分析IgAN患者的pIgA和IgA RF是否能够抑制正常人血清溶解在等价点形成的免疫沉淀物(牛血清白蛋白-抗牛血清白蛋白)的能力。结果显示,IgAN患者血清“体外”溶解免疫沉淀物的平均能力显著降低(p<0.001),血液中pIgA(p<0.001)和IgA RF(p<0.005)的平均水平显著升高。pIgA量的增加抑制了液相中IC的溶解,IgA RF也显示出抑制活性。pIgA与血清溶解IC的能力之间呈负相关(r = -0.36;p<0.05),IgA RF与补体介导的溶解之间呈负相关(r = -0.57;p<0.001)。提示pIgA和IgA RF可能是原发性IgAN患者血清补体介导的溶解受损以及血液中不溶性致肾炎IC持续存在的原因。