Broad spectrum of interferon-related nephropathies-glomerulonephritis, systemic lupus erythematosus-like syndrome and thrombotic microangiopathy: A case report and review of literature

I. Gianassi, M. Allinovi, L. Caroti, L. Cirami
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引用次数: 15

Abstract

BACKGROUND Interferons (IFNs) are characterized by a wide range of biological effects, which justifies their potential therapeutic use in several pathologies, but also elicit a wide array of adverse effects in almost every organ system. Among them, renal involvement is probably one of the most complex to identify. CASE SUMMARY We describe four cases of kidney damage caused by different IFN formulations: IFN-β-related thrombotic microangiopathy, IFN-β-induced systemic lupus erythematosus, and two cases of membranous nephropathy secondary to pegylated-IFN-α 2B. In each case, we carefully excluded any other possible cause of renal involvement. Once suspected as the casual relationship between drug and kidney damage, IFN treatment was immediately discontinued. In three cases, we observed a complete and persistent remission of clinical and laboratory abnormalities after IFN withdrawal, while the patient who developed thrombotic microangiopathy, despite IFN withdrawal and complement-inhibitor therapy with eculizumab, showed persistent severe renal failure requiring dialysis. CONCLUSION This case series highlights the causal relationship between IFN treatment and different types of renal involvement and enables us to delineate several peculiarities of this association.
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广谱干扰素相关性肾病——肾小球肾炎、系统性红斑狼疮样综合征和血栓性微血管病:1例报告并文献复习
干扰素(ifn)具有广泛的生物学效应,这证明了它们在几种疾病中的潜在治疗用途,但也会在几乎每个器官系统中引起广泛的不良反应。其中,肾脏受累可能是最复杂的识别之一。病例总结:我们描述了4例由不同的IFN制剂引起的肾损害:IFN-β相关的血栓性微血管病,IFN-β诱导的系统性红斑狼疮,以及2例继发于peg -IFN-α 2B的膜性肾病。在每个病例中,我们都仔细地排除了任何其他可能导致肾脏受累的原因。一旦怀疑药物与肾损害之间存在偶然关系,IFN治疗立即停止。在三个病例中,我们观察到IFN停药后临床和实验室异常的完全和持续缓解,而发生血栓性微血管病变的患者,尽管IFN停药并使用eculizumab进行补体抑制剂治疗,但仍表现出持续的严重肾功能衰竭,需要透析。结论:本病例系列强调了干扰素治疗与不同类型肾脏受累之间的因果关系,并使我们能够描述这种关联的几个特点。
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