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Quantitative study of mesangial injury with proteinuria induced by monoclonal antibody 1-22-3.

机译:单克隆抗体1-22-3诱导的肾小球系膜损伤与蛋白尿的定量研究。

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摘要

Murine MoAb 1-22-3 has already been reported to bind to the mesangial cell surface and to cause transient proteinuria and mesangial morphological changes characterized by mesangiolysis, subsequent mesangial cell proliferation and mesangial matrix increase by a single i.v. injection. In this study, MoAb-induced glomerulopathy was quantitatively analysed. No correlation between the severity of mesangial morphological changes and the degree of proteinuria was detected (r = 0.190). The minimum dose injected to induce abnormal proteinuria was 25 micrograms. This dose corresponded to 1.79 micrograms/2 kidneys 30 min after MoAb injection. The highest average level of proteinuria was observed in rats injected with 500 micrograms of MoAb, and less proteinuria was observed in rats injected with 10.0, 5.0 and 2.0 mg. Although the amounts of kidney-fixing MoAb and the subsequent deposition of rat C3 in the high-dose-injected group were larger than in the 500 micrograms injected group, the numbers of infiltrating inflammatory cells were the same in both groups. No correlations between the degrees of such mediators and proteinuria were observed.
机译:据报道,鼠MoAb 1-22-3与肾小球膜细胞表面结合,并引起短暂性蛋白尿和以血管溶血为特征的肾小球膜形态改变,随后的肾小球血管膜增生和肾小球膜基质增加。注射。在这项研究中,对MoAb引起的肾小球病进行了定量分析。肾小球膜形态学改变的严重程度与蛋白尿程度之间没有相关性(r = 0.190)。诱导异常蛋白尿的最低注射剂量为25微克。注射MoAb后30分钟,此剂量相当于1.79微克/ 2个肾脏。在注射500微克MoAb的大鼠中观察到最高的平均蛋白尿水平,而在注射10.0、5.0和2.0 mg的大鼠中观察到的蛋白尿较少。尽管高剂量注射组的肾脏固定MoAb数量和随后的大鼠C3沉积量大于500毫克注射组,但两组的浸润性炎症细胞数量相同。没有观察到这种介体的程度与蛋白尿之间的相关性。

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