首页> 美国卫生研究院文献>Clinical Kidney Journal >Rapid and sustained response to tocilizumab anti-interleukin-6 receptor antibody in a patient with nephrotic syndrome secondary to systemic juvenile idiopathic arthritis-related amyloidosis
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Rapid and sustained response to tocilizumab anti-interleukin-6 receptor antibody in a patient with nephrotic syndrome secondary to systemic juvenile idiopathic arthritis-related amyloidosis

机译:在系统性幼年特发性关节炎相关淀粉样变性继发的肾病综合征患者中对抗白细胞介素-6受体抗体tocilizumab的快速持续反应

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摘要

AA amyloidosis, or secondary amyloidosis, is a rare but serious complication of chronic inflammatory diseases. Chronic inflammatory arthritis is the commonest cause of AA amyloidosis and, when the latter appears, treatment can be frustrating. Deposition of fibrils, derived from circulating acute-phase reactant serum amyloid A protein (SAA), in the kidneys can lead to proteinuria and progressive loss of renal function. We describe the case of a 14-year-old female with systemic juvenile idiopathic arthritis who developed nephrotic syndrome secondary to AA amyloidosis; while she was unresponsive to all measures, including anti-tumour necrosis factor therapy, treatment with tocilizumab, an anti-human interleukin-6 receptor antibody, immediately normalized the SAA and reversed the nephrotic syndrome. We discuss this new therapeutic approach.
机译:AA淀粉样变性或继发性淀粉样变性是慢性炎性疾病的一种罕见但严重的并发症。慢性炎性关节炎是AA淀粉样变性的最常见原因,当后者出现时,治疗可能会令人沮丧。来自循环急性期反应物血清淀粉样蛋白A蛋白(SAA)的原纤维在肾脏中的沉积可导致蛋白尿和肾功能的逐步丧失。我们描述了一名患有系统性幼年特发性关节炎的14岁女性的案例,该女性发展为继发于AA淀粉样变性病的肾病综合征。尽管她对包括抗肿瘤坏死因子疗法在内的所有措施均无反应,但抗人白细胞介素6受体抗体托珠单抗治疗却使SAA正常化并逆转了肾病综合征。我们讨论了这种新的治疗方法。

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