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2
Bleomycin delivery by osmotic minipump: similarity to human scleroderma interstitial lung disease.通过渗透微型泵输送博来霉素:与人类硬皮病性间质性肺病的相似性。
Am J Physiol Lung Cell Mol Physiol. 2014 Apr 15;306(8):L736-48. doi: 10.1152/ajplung.00210.2013. Epub 2014 Feb 28.
3
Effects and safety of rituximab in systemic sclerosis: an analysis from the European Scleroderma Trial and Research (EUSTAR) group.利妥昔单抗治疗系统性硬化症的疗效和安全性:来自欧洲硬皮病试验和研究(EUSTAR)组的分析。
Ann Rheum Dis. 2015 Jun;74(6):1188-94. doi: 10.1136/annrheumdis-2013-204522. Epub 2014 Jan 17.
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Arthritis Res Ther. 2013 Sep 16;15(5):R120. doi: 10.1186/ar4300.
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Epstein-Barr virus infection induces aberrant TLR activation pathway and fibroblast-myofibroblast conversion in scleroderma.EB 病毒感染诱导硬皮病中异常的 TLR 激活途径和成纤维细胞-肌成纤维细胞转化。
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Integrin-modulating therapy prevents fibrosis and autoimmunity in mouse models of scleroderma.整合素调节疗法可预防硬皮病小鼠模型的纤维化和自身免疫。
Nature. 2013 Nov 7;503(7474):126-30. doi: 10.1038/nature12614. Epub 2013 Oct 9.
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Relaxin attenuates silica-induced pulmonary fibrosis by regulating collagen type I and MMP-2.松弛素通过调节Ⅰ型胶原和 MMP-2 减轻二氧化硅诱导的肺纤维化。
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系统性硬化症的动物模型:其效用与局限性

Animal models of systemic sclerosis: their utility and limitations.

作者信息

Artlett Carol M

机构信息

Department of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA, USA.

出版信息

Open Access Rheumatol. 2014 Jul 1;6:65-81. doi: 10.2147/OARRR.S50009. eCollection 2014.

DOI:10.2147/OARRR.S50009
PMID:27790036
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5045111/
Abstract

Without doubt, animal models have provided significant insights into our understanding of the rheumatological diseases; however, no model has accurately replicated all aspects of any autoimmune disease. Recent years have seen a plethora of knockouts and transgenics that have contributed to our knowledge of the initiating events of systemic sclerosis, an autoimmune disease. In this review, the focus is on models of systemic sclerosis and how they have progressed our understanding of fibrosis and vasculopathy, and whether they are relevant to the pathogenesis of systemic sclerosis.

摘要

毫无疑问,动物模型为我们理解风湿性疾病提供了重要的见解;然而,没有一种模型能准确复制任何自身免疫性疾病的所有方面。近年来,出现了大量的基因敲除和转基因动物模型,这些模型有助于我们了解系统性硬化症(一种自身免疫性疾病)的起始事件。在这篇综述中,重点是系统性硬化症的模型,以及它们如何推动我们对纤维化和血管病变的理解,以及它们是否与系统性硬化症的发病机制相关。