Welch T R, Kleesattel A, Beischel L
Children's Hospital Research Foundation, Division of Nephrology, Cincinnati, Ohio 45229-2899.
Clin Exp Immunol. 1988 Apr;72(1):103-7.
Inhibition of complement mediated solubilization (CMS) of preformed immune complexes was previously demonstrated in the serum of patients with systemic lupus erythematosus. We studied the ability of serum from patients with MPGN I or III to inhibit the solubilization of preformed BSA- anti-BSA aggregates by pooled normal human serum. Inhibition of CMS was found in the sera of 20/35 patients; the inhibition was more dramatic in those with active disease (9/9), as compared to those in remission (8/21) or with renal failure (3/5). The inhibition did not seem to be related to corticosteroid therapy, nephrotic syndrome, circulating immune complexes or hypocomplementaemia. In only one patient was inhibition associated with the presence of C3 nephritic factor activity and decomplementation of the target serum.
先前已证实在系统性红斑狼疮患者的血清中存在对预先形成的免疫复合物的补体介导溶解作用(CMS)的抑制。我们研究了I型或III型膜增生性肾小球肾炎(MPGN)患者血清抑制人混合正常血清对预先形成的牛血清白蛋白-抗牛血清白蛋白聚集体溶解的能力。在35例患者中的20例血清中发现了CMS抑制;与缓解期患者(8/21)或肾衰竭患者(3/5)相比,活动期疾病患者(9/9)的抑制作用更为显著。这种抑制似乎与皮质类固醇治疗、肾病综合征、循环免疫复合物或补体减少无关。仅1例患者的抑制作用与C3肾炎因子活性的存在及靶血清的补体分解有关。