The heterologous immune complex glomerulonephritis. A dose dependent glomerulonephritis with acute, latent and chronic phases in a long-term study.

B. Iversen, R. Matre, J. Ofstad
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引用次数: 6

Abstract

The pathophysiology, histology and immunohistology of acute and chronic heterologous immune complex glomerulonephritis were investigated in a long-term study in male Wistar rats. The glomerulonephritis showed 3 phases: an initial nephrotic syndrome, a latent phase with stable proteinuria (40 mg/24 h), and a terminal phase with increasing proteinuria and blood pressure, and declining serum protein concentration and creatinine clearance. Antiserum doses of 1.0, 1.5 and 2.0 ml induced maximal proteinuria (112, 257 and 272 mg/24 h respectively) after 14 days whereas normal rabbit serum and 0.5 ml antiserum gave no proteinuria. After 100 days, the rats injected with 1.0 ml of antiserum did not show physiological signs of renal disease; in the rats injected with 1.5 ml of antiserum the disease run a chronic course. Equal amounts of rabbit IgG, rat IgG and rat C3 were found in 10 glomeruli from rats 100 days after injection of 0.5, 1.0 and 2.0 ml (p greater than 0.10). Intramembranous deposits and spike formation were observed in all groups. All changes increased with greater antiserum doses. Chronically diseased animals observed from 500 to 750 days showed deposits of rabbit IgG in the basement membrane, and in most animals small amounts of rat IgG and rat C3 were also observed. This is compatible with a sustained stimulus for antibody formation throughout the course of this type of glomerulonephritis.
异源免疫复合物肾小球肾炎。剂量依赖性肾小球肾炎急性、潜伏期和慢性期的长期研究。
对雄性Wistar大鼠急性和慢性异源免疫复合物肾小球肾炎的病理生理、组织学和免疫组织学进行了研究。肾小球肾炎表现为3个阶段:初期肾病综合征,潜伏期稳定蛋白尿(40 mg/24 h),终末期蛋白尿和血压升高,血清蛋白浓度和肌酐清除率下降。1.0、1.5和2.0 ml抗血清在14天后诱导最大蛋白尿(分别为112、257和272 mg/24 h),而正常兔血清和0.5 ml抗血清无蛋白尿。100天后,注射1.0 ml抗血清的大鼠未出现肾脏疾病的生理征象;大鼠注射1.5 ml抗血清后,疾病呈慢性病程。注射0.5、1.0、2.0 ml后100 d, 10只大鼠肾小球中兔IgG、大鼠IgG和大鼠C3含量相等(p > 0.10)。各组均有膜内沉积和穗状突起形成。抗血清剂量越大,这些变化就越明显。500 ~ 750天观察的慢性病动物基底膜上可见兔IgG沉积,多数动物基底膜上也可见少量大鼠IgG和大鼠C3。这与在这种类型的肾小球肾炎的整个过程中持续刺激抗体形成是相容的。
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