系统性红斑狼疮的无瘤细胞抗体。

Pub Date : 2023-02-01 DOI:10.1358/dot.2023.59.2.3521876
Michael F Loncharich, Ian Robertson
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引用次数: 1

摘要

系统性红斑狼疮是一种复杂的自身免疫性疾病,具有不同的疾病表现和进展。羟氯喹和皮质类固醇是一线治疗方法。疾病的严重程度和器官系统的受累程度引导免疫调节药物在这些主要药物之外的升级。Anifrolumab是一种全球领先的1型干扰素抑制剂,最近被美国食品和药物管理局(FDA)批准用于系统性红斑狼疮的标准治疗。本文综述了1型干扰素在狼疮病理生理中的作用,以及导致anfrolumab获批的证据,重点介绍了MUSE、TULIP-1和TULIP-2试验。除了标准护理,anifrolumab可以减少皮质类固醇的需求,减少狼疮疾病的活动性,特别是皮肤和肌肉骨骼的表现,具有可接受的安全性。
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Anifrolumab in systemic lupus erythematosus.

Systemic lupus erythematosus is a complex autoimmune disease with variable disease presentation and progression. Hydroxychloroquine and corticosteroids are first-line therapies. Disease severity and organ system involvement guide escalation of immunomodulatory medications beyond these mainstays. Anifrolumab is a first-in-class global type 1 interferon inhibitor recently approved by the United States Food and Drug Administration (FDA) for systemic lupus erythematosus in addition to standard of care. This article reviews the role of type 1 interferons in lupus pathophysiology and the evidence leading to anifrolumab's approval with particular emphasis on the MUSE, TULIP-1 and TULIP-2 trials. In addition to standard of care, anifrolumab can reduce corticosteroid requirements and reduce lupus disease activity, especially skin and musculoskeletal manifestations, with an acceptable safety profile.

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