Institute for Biological Research "Sinisa Stankovic," Department of Neurobiology, University of Belgrade, Belgrade, Serbia.
Clinic for Infectious and Tropic Diseases, Military Medical Academy, Belgrade, Serbia.
J Neurosci Res. 2018 Jun;96(6):1021-1042. doi: 10.1002/jnr.24224. Epub 2018 Feb 15.
Multiple sclerosis (MS) is a chronic, progressive disorder of the central nervous system (CNS) that affects more than two million people worldwide. Several animal models resemble MS pathology; the most employed are experimental autoimmune encephalomyelitis (EAE) and toxin- and/or virus-induced demyelination. In this review we will summarize our knowledge on the utility of different animal models in MS research. Although animal models cannot replicate the complexity and heterogeneity of the MS pathology, they have proved to be useful for the development of several drugs approved for treatment of MS patients. This review focuses on EAE because it represents both clinical and pathological features of MS. During the past decades, EAE has been effective in illuminating various pathological processes that occur during MS, including inflammation, CNS penetration, demyelination, axonopathy, and neuron loss mediated by immune cells.
多发性硬化症(MS)是一种影响全球超过 200 万人的中枢神经系统(CNS)慢性、进行性疾病。有几种动物模型类似于 MS 病理学;最常用的是实验性自身免疫性脑脊髓炎(EAE)和毒素-和/或病毒诱导的脱髓鞘。在这篇综述中,我们将总结我们对不同动物模型在 MS 研究中的应用的了解。虽然动物模型不能复制 MS 病理学的复杂性和异质性,但它们已被证明对几种批准用于治疗 MS 患者的药物的开发有用。本综述重点介绍 EAE,因为它代表了 MS 的临床和病理特征。在过去几十年中,EAE 有效地阐明了 MS 期间发生的各种病理过程,包括炎症、CNS 穿透、脱髓鞘、轴突病和免疫细胞介导的神经元丧失。