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抗体作为多发性硬化症病理生理过程的生物标志物。

Antibodies as biological markers for pathophysiological processes in MS.

作者信息

Reindl Markus, Khalil Michael, Berger Thomas

机构信息

Clinical Department of Neurology, Innsbruck Medical University, Anichstrasse 35, A-6020 Innsbruck, Austria.

出版信息

J Neuroimmunol. 2006 Nov;180(1-2):50-62. doi: 10.1016/j.jneuroim.2006.06.028. Epub 2006 Aug 23.

Abstract

Multiple sclerosis (MS), the most important human inflammatory demyelinating disease of the central nervous system, is characterized by various clinical disease courses, inhomogeneous and unpredictable therapeutic effects, heterogenous genetic backgrounds and immunopathogenetic subtypes as demonstrated by neuropathology. Because of this heterogeneity of MS, a subtyping of our patients by genetical, clinical, neuroradiological, and neuroimmunological parameters will be necessary in the future. Therefore the importance of identifying biological markers for MS has evolved over the past years. Evidence for a possible role of antibodies as biological markers for MS comes from several studies indicating that intrathecal antibody production and the dominance of B cells are associated with a more progressive disease course. In this review we will give an overview on the current status and potential applicability of antibodies as biological markers for the diagnosis, classification, disease activity and prediction of clinical courses in MS. We will therefore summarize the findings on autoantibodies to myelin and nonmyelin antigens and on viral antigens in MS. We believe that antibodies serving as biomarkers will help to establish a differential therapeutic concept in MS, which will allow to treat individuals selectively according to their pathogenetic subtype and disease status.

摘要

多发性硬化症(MS)是人类最重要的中枢神经系统炎性脱髓鞘疾病,其特点是具有多种临床病程、治疗效果不均一且难以预测、遗传背景各异以及神经病理学显示的免疫发病机制亚型不同。由于MS存在这种异质性,未来有必要根据遗传学、临床、神经放射学和神经免疫学参数对患者进行亚型分类。因此,在过去几年中,识别MS生物学标志物的重要性日益凸显。多项研究表明鞘内抗体产生和B细胞优势与更进展性的病程相关,这些研究为抗体作为MS生物学标志物的可能作用提供了证据。在本综述中,我们将概述抗体作为MS诊断、分类、疾病活动度及临床病程预测的生物学标志物的现状和潜在适用性。因此,我们将总结MS中针对髓鞘和非髓鞘抗原以及病毒抗原的自身抗体的研究结果。我们认为,作为生物标志物的抗体将有助于建立MS的差异化治疗概念,从而能够根据个体的发病机制亚型和疾病状态进行选择性治疗。

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