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干扰素在成人斯蒂尔病和巨噬细胞活化综合征的高炎症反应中的致病作用:为新治疗靶点铺平道路。

The Pathogenic Role of Interferons in the Hyperinflammatory Response on Adult-Onset Still's Disease and Macrophage Activation Syndrome: Paving the Way towards New Therapeutic Targets.

作者信息

Di Cola Ilenia, Ruscitti Piero, Giacomelli Roberto, Cipriani Paola

机构信息

Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, 67100 L'Aquila, Italy.

Rheumatology and Immunology Unit, Department of Medicine, University of Rome Campus Biomedico, 00128 Rome, Italy.

出版信息

J Clin Med. 2021 Mar 10;10(6):1164. doi: 10.3390/jcm10061164.

Abstract

Adult-onset Still's disease (AOSD) is a systemic inflammatory disorder of unknown aetiology affecting young adults, which is burdened by life-threatening complications, mostly macrophage activation syndrome (MAS). Interferons (IFNs) are signalling molecules that mediate a variety of biological functions from defence against viral infections, to antitumor and immunomodulatory effects. These molecules have been classified into three major types: IFN I, IFN II, IFN III, presenting specific characteristics and functions. In this work, we reviewed the role of IFNs on AOSD and MAS, focusing on their pathogenic role in promoting the hyperinflammatory response and as new possible therapeutic targets. In fact, both preclinical and clinical observations suggested that these molecules could promote the hyperinflammatory response in MAS during AOSD. Furthermore, the positive results of inhibiting IFN-γ in primary hemophagocytic lymphohistiocytosis may provide a solid rationale to arrange further clinical studies, paving the way for reducing the high mortality rate in MAS during AOSD.

摘要

成人斯蒂尔病(AOSD)是一种病因不明的系统性炎症性疾病,影响年轻人,常伴有危及生命的并发症,主要是巨噬细胞活化综合征(MAS)。干扰素(IFN)是一类信号分子,介导多种生物学功能,从抵御病毒感染到抗肿瘤和免疫调节作用。这些分子已被分为三大类:I型干扰素、II型干扰素、III型干扰素,各有特定的特征和功能。在这项工作中,我们综述了干扰素在AOSD和MAS中的作用,重点关注它们在促进过度炎症反应中的致病作用以及作为新的潜在治疗靶点的作用。事实上,临床前和临床观察均表明,这些分子可在AOSD期间促进MAS中的过度炎症反应。此外,在原发性噬血细胞性淋巴组织细胞增生症中抑制IFN-γ的阳性结果可能为开展进一步临床研究提供有力依据,为降低AOSD期间MAS的高死亡率铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b00/7999936/5627c0b8cd30/jcm-10-01164-g001.jpg

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