• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

JAK抑制剂鲁索替尼可抑制皮肤红斑狼疮特征性细胞因子的表达。

JAK inhibitor ruxolitinib inhibits the expression of cytokines characteristic of cutaneous lupus erythematosus.

作者信息

Klaeschen Anna Sophie, Wolf Dominik, Brossart Peter, Bieber Thomas, Wenzel Joerg

机构信息

Department of Dermatology and Allergy, University Hospital Bonn, Bonn, Germany.

Medical Clinic III, Hematology, Oncology and Rheumatology, University Hospital of Bonn, Bonn, Germany.

出版信息

Exp Dermatol. 2017 Aug;26(8):728-730. doi: 10.1111/exd.13253. Epub 2017 May 3.

DOI:10.1111/exd.13253
PMID:27892610
Abstract

This study was stimulated by the clinical observation of a rapid response of a chilblain lupus patient to treatment with JAK1/2-kinase inhibitor ruxolitinib. We investigated the in vivo expression of phospho-JAK2 in CLE skin samples as well as the immunomodulatory in vitro effect of ruxolitinib in cultured immortalized keratinocytes and in a 3D human epidermis model (epiCS). Our results demonstrate that ruxolitinib significantly decreases the production of CLE-typical cytokines (CXCL10, CXCL9, MxA) and might be a promising drug for future clinical studies in patients with CLE and related autoimmune skin diseases.

摘要

本研究受冻疮样狼疮患者对JAK1/2激酶抑制剂鲁索替尼治疗产生快速反应的临床观察启发。我们研究了CLE皮肤样本中磷酸化JAK2的体内表达,以及鲁索替尼在培养的永生化角质形成细胞和三维人表皮模型(epiCS)中的体外免疫调节作用。我们的结果表明,鲁索替尼显著降低了CLE典型细胞因子(CXCL10、CXCL9、Mx A)的产生,可能是未来用于CLE及相关自身免疫性皮肤病患者临床研究的一种有前景的药物。

相似文献

1
JAK inhibitor ruxolitinib inhibits the expression of cytokines characteristic of cutaneous lupus erythematosus.JAK抑制剂鲁索替尼可抑制皮肤红斑狼疮特征性细胞因子的表达。
Exp Dermatol. 2017 Aug;26(8):728-730. doi: 10.1111/exd.13253. Epub 2017 May 3.
2
Selective Janus Kinase 1 Inhibition Is a Promising Therapeutic Approach for Lupus Erythematosus Skin Lesions.选择性 Janus 激酶 1 抑制是治疗红斑狼疮皮肤损伤的一种有前途的治疗方法。
Front Immunol. 2020 Mar 3;11:344. doi: 10.3389/fimmu.2020.00344. eCollection 2020.
3
JAK1/2 Inhibitor Ruxolitinib Controls a Case of Chilblain Lupus Erythematosus.JAK1/2抑制剂芦可替尼治疗1例冻疮样狼疮
J Invest Dermatol. 2016 Jun;136(6):1281-1283. doi: 10.1016/j.jid.2016.02.015. Epub 2016 Feb 23.
4
Assessment of Clinical Response to Janus Kinase Inhibition in Patients With Familial Chilblain Lupus and TREX1 Mutation.评估家族性寒冷性自身免疫性荨麻疹样狼疮和 TREX1 突变患者对 Janus 激酶抑制的临床反应。
JAMA Dermatol. 2019 Mar 1;155(3):342-346. doi: 10.1001/jamadermatol.2018.5077.
5
Spleen tyrosine kinase (SYK) is a potential target for the treatment of cutaneous lupus erythematosus patients.脾酪氨酸激酶(SYK)是治疗皮肤红斑狼疮患者的一个潜在靶点。
Exp Dermatol. 2016 May;25(5):375-9. doi: 10.1111/exd.12986.
6
Enhanced type I interferon signalling promotes Th1-biased inflammation in cutaneous lupus erythematosus.增强的I型干扰素信号传导促进皮肤红斑狼疮中以Th1为主的炎症反应。
J Pathol. 2005 Mar;205(4):435-42. doi: 10.1002/path.1721.
7
Repression of interferon β-regulated cytokines by the JAK1/2 inhibitor ruxolitinib in inflammatory human macrophages.JAK1/2 抑制剂芦可替尼抑制炎症性人巨噬细胞中干扰素 β 调节的细胞因子。
Int Immunopharmacol. 2018 Jan;54:354-365. doi: 10.1016/j.intimp.2017.11.032. Epub 2017 Dec 1.
8
Immunostimulatory Endogenous Nucleic Acids Drive the Lesional Inflammation in Cutaneous Lupus Erythematosus.免疫刺激性内源性核酸驱动皮肤红斑狼疮的皮损炎症。
J Invest Dermatol. 2017 Jul;137(7):1484-1492. doi: 10.1016/j.jid.2017.03.018. Epub 2017 Mar 27.
9
NKG2D and its ligands as cytotoxic factors in cutaneous lupus erythematosus.NKG2D 及其配体作为皮肤红斑狼疮的细胞毒性因子。
Exp Dermatol. 2021 Jun;30(6):847-852. doi: 10.1111/exd.14311. Epub 2021 Mar 9.
10
Efficacy of JAK1/2 inhibition in the treatment of chilblain lupus due to TREX1 deficiency.JAK1/2抑制在治疗因TREX1缺乏引起的冻疮样狼疮中的疗效。
Ann Rheum Dis. 2019 Mar;78(3):431-433. doi: 10.1136/annrheumdis-2018-214037. Epub 2018 Oct 3.

引用本文的文献

1
Immune cell senescence in autoimmunity: implications for disease pathogenesis and therapeutic targeting.自身免疫中的免疫细胞衰老:对疾病发病机制和治疗靶点的影响
Front Immunol. 2025 Aug 7;16:1596686. doi: 10.3389/fimmu.2025.1596686. eCollection 2025.
2
JAK-STAT Signaling in Autoimmunity and Cancer.自身免疫与癌症中的JAK-STAT信号传导
Immunotargets Ther. 2025 May 11;14:523-554. doi: 10.2147/ITT.S485670. eCollection 2025.
3
Ruxolitinib synergizes with regulatory T cells to improve inflammation but has no added benefits in decreasing albuminuria in SLE.
鲁索替尼与调节性T细胞协同作用以改善炎症,但在降低系统性红斑狼疮患者的蛋白尿方面并无额外益处。
Front Immunol. 2025 Feb 5;16:1449693. doi: 10.3389/fimmu.2025.1449693. eCollection 2025.
4
Molecular and cellular mechanisms of itch sensation and the anti-itch drug targets.瘙痒感觉的分子和细胞机制以及抗瘙痒药物靶点。
Acta Pharmacol Sin. 2025 Mar;46(3):539-553. doi: 10.1038/s41401-024-01400-x. Epub 2024 Oct 18.
5
An update on clinical trials for cutaneous lupus erythematosus.皮肤红斑狼疮临床试验的最新进展。
J Dermatol. 2024 Jul;51(7):885-894. doi: 10.1111/1346-8138.17161. Epub 2024 Mar 15.
6
Novel heterozygous mutation in a juvenile systemic lupus erythematosus patient with severe cutaneous involvement treated successfully with Jak-inhibitors: a case report.新型杂合突变的幼年系统性红斑狼疮患者出现严重皮肤受累,经 Jak 抑制剂治疗成功:病例报告。
Front Immunol. 2023 Dec 6;14:1288675. doi: 10.3389/fimmu.2023.1288675. eCollection 2023.
7
Single-Cell Transcriptome Analysis Identifies Subclusters with Inflammatory Fibroblast Responses in Localized Scleroderma.单细胞转录组分析鉴定局限性硬皮病中具有炎症性成纤维细胞反应的亚群。
Int J Mol Sci. 2023 Jun 6;24(12):9796. doi: 10.3390/ijms24129796.
8
Why Do We Need JAK Inhibitors in Systemic Lupus Erythematosus?为什么我们需要 JAK 抑制剂治疗系统性红斑狼疮?
Int J Mol Sci. 2022 Oct 4;23(19):11788. doi: 10.3390/ijms231911788.
9
An update on the management of refractory cutaneous lupus erythematosus.难治性皮肤红斑狼疮的治疗进展
Front Med (Lausanne). 2022 Sep 23;9:941003. doi: 10.3389/fmed.2022.941003. eCollection 2022.
10
The Genetic Landscape of Cutaneous Lupus Erythematosus.皮肤红斑狼疮的遗传图谱
Front Med (Lausanne). 2022 Jun 2;9:916011. doi: 10.3389/fmed.2022.916011. eCollection 2022.