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Glomerular deposition of properdin in acute and chronic glomerulonephritis with hypocomplementemia

机译:备解素在急慢性肾小球肾炎合并低补体血症的肾小球沉积

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摘要

Kidney tissue from 97 patients was studied by immunofluorescent techniques using antiserum to purified properdin. All patients with acute poststreptococcal glomerulonephritis showed deposition of properdin and the third component of complement (C3), either as “humps” on the basement membrane, or in the mesangium. In all cases of chronic membranoproliferative glomerulonephritis, properdin and C3 were localized in the glomeruli, most commonly in a lobular pattern on the basement membrane. Activation of C3 by the properdin system may explain the depressed serum levels of C3 and terminal complement components even though levels of earlier components are normal, and the deposition of C3, often without immunoglobulins, in the kidneys of patients with acute glomerulonephritis or chronic membranoproliferative glomerulonephritis.
机译:通过免疫荧光技术使用抗血清对纯化的备解素进行研究,研究了来自97名患者的肾脏组织。所有患有急性链球菌性肾小球肾炎的患者均显示备解素和补体第三成分(C3)的沉积,以“驼峰”形式出现在基底膜或系膜上。在所有慢性膜增生性肾小球肾炎的病例中,备解素和C3均位于肾小球,最常见的是在基膜上呈小叶状分布。备解素系统激活C3可能解释了C3和终末补体成分的血清水平降低,即使较早的成分水平正常,以及C3在急性肾小球肾炎或慢性膜化增生性肾小球肾炎患者肾脏中的沉积(通常没有免疫球蛋白) 。

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