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1 型干扰素与肌炎。

Type 1 interferons and myositis.

机构信息

Department of Neurology, Division of Neuromuscular Disease, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA.

出版信息

Arthritis Res Ther. 2010;12 Suppl 1(Suppl 1):S4. doi: 10.1186/ar2885. Epub 2010 Apr 14.

DOI:10.1186/ar2885
PMID:20392291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2991777/
Abstract

Recent studies suggest a mechanistic role for molecules induced by type 1 interferons in the pathogenesis of some forms of myositis. For dermatomyositis, evidence that these molecules injure myofibers seems especially strong. In the group of disorders known as polymyositis, the study of blood samples suggests a potential role. It is unknown what drives the sustained presence of type 1 interferon-inducible molecules in these diseases, as the type 1 interferons themselves have not been specifically detected along with their downstream biomarkers. Therapeutic development for blockade of IFNα is in progress aided by the identification of blood genomic biomarkers.

摘要

最近的研究表明,1 型干扰素诱导的分子在某些形式的肌炎发病机制中起作用。对于皮肌炎,这些分子损伤肌纤维的证据似乎尤为有力。在被称为多发性肌炎的一组疾病中,对血液样本的研究表明了其潜在作用。目前尚不清楚是什么导致这些疾病中 1 型干扰素诱导分子持续存在,因为尚未特异性检测到 1 型干扰素及其下游生物标志物。通过鉴定血液基因组生物标志物,有助于 IFNα 阻断的治疗开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/006b/2991777/dde14f4c4222/ar2885-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/006b/2991777/f023ea5990a6/ar2885-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/006b/2991777/fedfbf6d3b98/ar2885-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/006b/2991777/4ee145f4bd73/ar2885-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/006b/2991777/160dea328ce9/ar2885-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/006b/2991777/dde14f4c4222/ar2885-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/006b/2991777/f023ea5990a6/ar2885-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/006b/2991777/fedfbf6d3b98/ar2885-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/006b/2991777/4ee145f4bd73/ar2885-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/006b/2991777/160dea328ce9/ar2885-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/006b/2991777/dde14f4c4222/ar2885-5.jpg

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本文引用的文献

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Interferon-stimulated gene 15 (ISG15) conjugates proteins in dermatomyositis muscle with perifascicular atrophy.干扰素刺激基因 15(ISG15)将皮肌炎肌肉中的蛋白与筋膜旁萎缩相关联。
Ann Neurol. 2010 Jan;67(1):53-63. doi: 10.1002/ana.21805.
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Inflammatory myopathies: disease mechanisms.炎性肌病:发病机制
Curr Opin Neurol. 2009 Oct;22(5):516-23. doi: 10.1097/WCO.0b013e3283311ddf.
3
RNA helicase encoded by melanoma differentiation-associated gene 5 is a major autoantigen in patients with clinically amyopathic dermatomyositis: Association with rapidly progressive interstitial lung disease.
主要组织相容性复合体(MHC)I过表达与I型干扰素的组合可诱导人骨骼肌成肌细胞中的线粒体功能障碍。
J Cell Physiol. 2025 Jan;240(1):e31458. doi: 10.1002/jcp.31458. Epub 2024 Oct 9.
4
Genetic changes from type I interferons and JAK inhibitors: clues to drivers of juvenile dermatomyositis.Ⅰ型干扰素和 JAK 抑制剂引起的遗传变化:幼年皮肌炎驱动因素的线索。
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Systemic Inflammatory Disorders, Immunosuppressive Treatment and Increase Risk of Head and Neck Cancers-A Narrative Review of Potential Physiopathological and Biological Mechanisms.系统性炎症疾病、免疫抑制治疗与头颈部癌症风险增加:潜在病理生理学和生物学机制的综述。
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Biological Therapies in Inflammatory Myopathies.炎症性肌病的生物疗法
Rambam Maimonides Med J. 2023 Apr 30;14(2):e0008. doi: 10.5041/RMMJ.10495.
7
Immune-mediated lung diseases: A narrative review.免疫介导的肺部疾病:一篇叙述性综述。
Front Med (Lausanne). 2023 Apr 6;10:1160755. doi: 10.3389/fmed.2023.1160755. eCollection 2023.
8
Identification of hub biomarkers and immune cell infiltration characteristics of polymyositis by bioinformatics analysis.基于生物信息学分析鉴定多发性肌炎的枢纽生物标志物和免疫细胞浸润特征。
Front Immunol. 2022 Sep 26;13:1002500. doi: 10.3389/fimmu.2022.1002500. eCollection 2022.
9
Management of Anti-melanoma Differentiation-Associated Gene 5 (Anti-MDA5)-Positive Dermatomyositis in an Acute Rehabilitation Center: A Case Report.急性康复中心抗黑色素瘤分化相关基因5(抗MDA5)阳性皮肌炎的管理:一例报告
Cureus. 2022 Aug 8;14(8):e27791. doi: 10.7759/cureus.27791. eCollection 2022 Aug.
10
A glance into the future of myositis therapy.肌炎治疗的未来展望。
Ther Adv Musculoskelet Dis. 2022 May 24;14:1759720X221100299. doi: 10.1177/1759720X221100299. eCollection 2022.
黑色素瘤分化相关基因5编码的RNA解旋酶是临床无肌病性皮肌炎患者的主要自身抗原:与快速进展性间质性肺病的关联。
Arthritis Rheum. 2009 Jul;60(7):2193-200. doi: 10.1002/art.24621.
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Open-label trial of anti-TNF-alpha in dermato- and polymyositis treated concomitantly with methotrexate.抗TNF-α联合甲氨蝶呤治疗皮肌炎的开放标签试验。
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Augmented interferon-alpha pathway activation in patients with Sjögren's syndrome treated with etanercept.接受依那西普治疗的干燥综合征患者中干扰素-α 通路激活增强。
Arthritis Rheum. 2007 Dec;56(12):3995-4004. doi: 10.1002/art.23062.
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Type I interferon-inducible gene expression in blood is present and reflects disease activity in dermatomyositis and polymyositis.血液中I型干扰素诱导基因表达存在,且反映皮肌炎和多肌炎的疾病活动情况。
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