Suppr超能文献

甘露糖结合凝集素介导的补体途径在自身免疫性神经系统疾病中的作用

Mannose-binding Lectin Mediated Complement Pathway in Autoimmune Neurological Disorders.

作者信息

Farrokhi Mehrdad, Dabirzadeh Mehrnoosh, Dastravan Nastaran, Etemadifar Masoud, Ghadimi Keyvan, Saadatpour Zahra, Rezaei Ali

机构信息

Department of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

Department of Neurology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Iran J Allergy Asthma Immunol. 2016 Jun;15(3):251-6.

Abstract

Multiple sclerosis (MS) is a complex, demyelinating disease of the central nervous system (CNS) with variable phenotypic presentations, while Guillain-Barre Syndrome (GBS) is the prototypic acute inflammatory disorder that affects the peripheral nervous system. Myasthenia gravis (MG) is a T cell dependent and antibody mediated autoimmune disease. Although it has been shown that complement plays a critical role in the pathogenesis of MS, GBS, and MG, the role of mannose-binding lectin (MBL) as a biomarker of immunopathogensis of these diseases and also its association with the severity of them have been poorly investigated. Therefore, in this study we aimed to measure plasma levels of MBL in patients with MS, GBS, and MG. In a case-control study, plasma was obtained from healthy controls (n=100) and also patients with MS (n=120), GBS (n=30), and MG (n=30). Plasma level measurement of MBL was performed using enzyme-linked immunosorbent assay (ELISA). The mean serum level of MBL was significantly different between groups of patients and healthy controls (p<0.001). We also found a positive correlation between plasma levels of MBL and severity scores of MS, MG, and GBS patients including: expanded disability status scale (EDSS) (r=+0.60 and p=<0.001), quantitative myasthenia gravis score (QMGS) (r=+0.56 and p=0.01), and GBS disability scale (GDS) (r=+0.37 and p=0.04). Taken together, our findings suggest that complement activation mediated by MBL contributes to the pathogenesis and also severity of MS, MG, and GBS. However, because the lectin pathway can be involved in several phases of the immune response, further evidence will be required to elucidate the underlying mechanism.

摘要

多发性硬化症(MS)是一种复杂的中枢神经系统(CNS)脱髓鞘疾病,具有多种表型表现,而吉兰-巴雷综合征(GBS)是影响周围神经系统的典型急性炎症性疾病。重症肌无力(MG)是一种T细胞依赖性和抗体介导的自身免疫性疾病。尽管已经表明补体在MS、GBS和MG的发病机制中起关键作用,但甘露糖结合凝集素(MBL)作为这些疾病免疫发病机制的生物标志物的作用及其与疾病严重程度的关联尚未得到充分研究。因此,在本研究中,我们旨在测量MS、GBS和MG患者的血浆MBL水平。在一项病例对照研究中,从健康对照者(n = 100)以及MS患者(n = 120)、GBS患者(n = 30)和MG患者(n = 30)中获取血浆。使用酶联免疫吸附测定(ELISA)进行MBL的血浆水平测量。患者组和健康对照组之间MBL的平均血清水平存在显著差异(p < 0.001)。我们还发现MBL的血浆水平与MS、MG和GBS患者的严重程度评分之间存在正相关,包括:扩展残疾状态量表(EDSS)(r = +0.60,p = <0.001)、重症肌无力定量评分(QMGS)(r = +0.56,p = 0.01)和GBS残疾量表(GDS)(r = +0.37,p = 0.04)。综上所述,我们的研究结果表明,MBL介导的补体激活有助于MS、MG和GBS的发病机制以及严重程度。然而,由于凝集素途径可能参与免疫反应的多个阶段,因此需要进一步的证据来阐明潜在机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验