Kurunczi S, Mark I
St. Josef-Hospital, Universitätsklinik Bochum, Deutschland.
Zentralbl Pathol. 1992;138(1):9-14.
Studies were conducted into the roles played by various duck immunoglobulins in the anti-basal membrane of nephrotoxic nephritis in rabbit. The 7.8S and 5.7S immunoglobulins which originated from nephrotoxic duck serum were found to be responsible for the development of nephritis in rabbit. No pathogenetic role was played by any other proteins of duck serum. The affinity for the glomerulus basal membrane of 7.8S immunoglobulin was found to be higher than that of 5.7S globulin. As to trigger dosage, nephritis was safely inducted by 10 mg/kg body weight (BW) in the context of 7.8S immunoglobulins and by 15 mg/kg BW in the case of 5.7S immunoglobulins. One and the same morphological nature was recorded from nephritis, no matter by which of the above immunoglobulins it had been caused. Nephrotoxic duck immunoglobulins proved to be highly suitable for induction of experimental glomerulonephritis due to absence from this model of the heterologous phase of nephritis. Hence, the autologous phase is unambiguous and can be examined with higher accuracy.
对各种鸭免疫球蛋白在兔肾毒性肾炎抗基底膜中的作用进行了研究。发现源自肾毒性鸭血清的7.8S和5.7S免疫球蛋白是导致兔肾炎发生的原因。鸭血清中的任何其他蛋白质均无致病作用。发现7.8S免疫球蛋白对肾小球基底膜的亲和力高于5.7S球蛋白。关于引发剂量,在7.8S免疫球蛋白的情况下,10mg/kg体重(BW)可安全诱导肾炎,在5.7S免疫球蛋白的情况下,15mg/kg BW可安全诱导肾炎。无论由上述哪种免疫球蛋白引起,肾炎的形态学性质都是相同的。由于该模型不存在肾炎的异源期,肾毒性鸭免疫球蛋白被证明非常适合诱导实验性肾小球肾炎。因此,同源期是明确的,可以更准确地进行研究。