将 JAK 抑制作为系统性红斑狼疮的潜在治疗靶点

Q4 Medicine Mediterranean Journal of Rheumatology Pub Date : 2024-03-30 eCollection Date: 2024-03-01 DOI:10.31138/mjr.231123.jia
Georgia-Savina Moysidou, Athanasia Dara
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引用次数: 0

摘要

Janus 激酶(JAK)/信号转导和转录激活因子(STATs)是一组分子,负责不同类型细胞中多种细胞因子和生长因子的信号转导,参与免疫耐受的维持。因此,这一通路的失调在多种自身免疫性、炎症性和过敏性疾病的发病机制中起着至关重要的作用,是一个极具吸引力的治疗靶点。JAK 抑制剂(JAKinibs)已被批准用于治疗多种自身免疫性疾病,包括类风湿性关节炎(RA)、银屑病关节炎(PsA)和强直性脊柱炎(SPA)。在系统性红斑狼疮方面,有大量正在进行的试验正在评估它们的疗效,其中托法替尼、巴利替尼和德拉瓦替尼显示出了良好的效果,而且没有重大的安全性问题。在这篇综述中,我们将讨论在系统性红斑狼疮中使用 JAKinibs 的理由,并总结 JAKinibs 在系统性红斑狼疮患者中的疗效和安全性的临床数据。
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JAK Inhibition as a Potential Treatment Target in Systemic Lupus Erythematosus.

Janus kinase (JAK)/signal transducers and activators of transcription (STATs) are a group of molecules responsible for signal transduction of multiple cytokines and growth factors in different cell types, involved in the maintenance of immune tolerance. Thus, the dysregulation of this pathway plays a crucial role in the pathogenesis of multiple autoimmune, inflammatory, and allergic diseases and is an attractive treatment target. JAK inhibitors (JAKinibs) have been approved in the treatment of multiple autoimmune diseases including rheumatoid arthritis (RA), psoriatic arthritis (PsA) and ankylosing spondylitis (SPA). In SLE, there is a plethora of ongoing trials evaluating their efficacy, with tofacitinib, baricitinib and deucravacitinib showing promising results, without major safety concerns. In this review, we will discuss the rationale of targeting JAKinibs in SLE and summarize the clinical data of efficacy and safety of JAKinibs in SLE patients.

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来源期刊
CiteScore
2.00
自引率
0.00%
发文量
42
审稿时长
8 weeks
期刊最新文献
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