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系统性硬化症中的树突状细胞:来自人类和小鼠研究的进展。

Dendritic cells in systemic sclerosis: Advances from human and mice studies.

机构信息

Laboratory of Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands; Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.

Laboratory of Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands; Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.

出版信息

Immunol Lett. 2018 Mar;195:18-29. doi: 10.1016/j.imlet.2017.11.003. Epub 2017 Nov 7.

Abstract

Systemic sclerosis (SSc) is a complex heterogeneous fibrotic autoimmune disease with an unknown exact etiology, and characterized by three hallmarks: fibrosis, vasculopathy, and immune dysfunction. Dendritic cells (DCs) are specialized cells in pathogen sensing with high potency of antigen presentation and capable of releasing mediators to shape the immune response. Altered DCs distributions and their impaired functions may account for their role in breaking the immune tolerance and driving inflammation in SSc, and the direct contribution of DCs in promoting endothelial dysfunction and fibrotic process has only begun to be understood. Plasmacytoid dendritic cells in particular have been implicated due to their high production of type I interferon as well as other cytokines and chemokines, including the pro-inflammatory and anti-angiogenic CXCL4. Furthermore, a deeper understanding of human and mouse DC biology has clarified their identification and function in different tissues, and novel DC subsets have only recently been discovered. In this review, we highlight key findings and recent advances exploring DC role in the pathogenesis of SSc and other related autoimmune diseases, and consideration of their potential use as targeted therapy in SSc.

摘要

系统性硬化症(SSc)是一种复杂的异质性纤维化自身免疫性疾病,其确切病因尚不清楚,其特征为三个标志:纤维化、血管病变和免疫功能障碍。树突状细胞(DCs)是具有高抗原呈递能力的病原体感应的专门细胞,能够释放介质来塑造免疫反应。DCs 的分布改变及其功能受损可能是其在打破 SSc 中的免疫耐受和驱动炎症中的作用的原因,而 DCs 在促进内皮功能障碍和纤维化过程中的直接作用才刚刚开始被理解。浆细胞样树突状细胞(pDCs)由于其高水平地产生 I 型干扰素以及其他细胞因子和趋化因子,包括促炎和抗血管生成的 CXCL4,因此尤其受到关注。此外,对人和小鼠 DC 生物学的更深入了解澄清了它们在不同组织中的鉴定和功能,并且最近才发现了新型 DC 亚群。在这篇综述中,我们重点介绍了探索 DC 在 SSc 和其他相关自身免疫性疾病发病机制中的作用的关键发现和最新进展,并考虑了它们作为 SSc 靶向治疗的潜在用途。

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