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Taking the kidney personally: The quest for novel antigens of idiopathic membranous nephropathy through proteomic approaches - per ardua ad astra?

机译:亲自面对肾脏:通过蛋白质组学方法寻求特发性膜性肾病的新型抗原

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摘要

Membranous nephropathy is one of the most common diseases affecting the glomerulus, an important part of the kidney responsible for filtration of blood. Glomeruli are networks of capillaries that filter blood; normally only small ions and proteins are filtered, while larger proteins like hemoglobin, albumin, and immunoglobulins are retained. The filtration barrier consists of several layers including: capillary endothelial cells, glomerular basement membrane, and specialized cells called podocytes. In patients with membranous nephropathy, this selective barrier is injured, leading to massive loss of proteins in urine (proteinuria). Patients typically present with marked swelling due to protein loss and avid sodium absorption by the kidneys, as well as hypoalbuminemia, hyperlipidemia, lipiduria, and propensity for developing infections and clots (called nephrotic syndrome).
机译:膜性肾病是影响肾小球的最常见疾病之一,肾小球是肾脏的重要组成部分,负责血液过滤。肾小球是过滤血液的毛细血管网络。通常只过滤小的离子和蛋白质,而保留较大的蛋白质,例如血红蛋白,白蛋白和免疫球蛋白。过滤屏障由几层组成,包括:毛细血管内皮细胞,肾小球基底膜和称为足细胞的专门细胞。在膜性肾病患者中,这种选择性屏障受到损害,导致尿液中大量蛋白质损失(蛋白尿)。由于蛋白质损失和肾脏对钠的狂热吸收,以及低白蛋白血症,高脂血症,脂质尿和感染和血栓形成的倾向(通常称为肾病综合征),患者通常会出现明显的肿胀。

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