Department of Immunology, Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Department of Medical Oncology, National Center for Tumor Diseases, Heidelberg University Hospital, Heidelberg, Germany.
J Neuroimmunol. 2019 Dec 15;337:577061. doi: 10.1016/j.jneuroim.2019.577061. Epub 2019 Sep 5.
Multiple sclerosis (MS) is the most common demyelinating disease which mainly impacts the integrity of central nervous system (CNS). MS etiology is not clearly known but genetic, environmental factors and immune system are the most frequently explored risk factors. Adaptive immune responses have a critical role in MS pathogenesis in which auto-reactive T-cells and autoantibodies are main orchestrators. Immune responses are modulated by inhibitory molecules which regulates adaptive system activation and hemostasis interface. These molecules suppress immune responses through inhibition of cytokine secretion and T cell proliferation and subsequently reducing the inflammation and respective damage. Therefore the critical role of inhibitory molecules in regulating the healthy and safe immune responses make them very attractive target for immunotherapy. In this review paper, the role of inhibitory molecules expressed on the various immune cell types in MS pathogenesis and experimental autoimmune encephalomyelitis (EAE) animal model will be summarized.
多发性硬化症(MS)是最常见的脱髓鞘疾病,主要影响中枢神经系统(CNS)的完整性。MS 的病因尚不清楚,但遗传、环境因素和免疫系统是最常被探讨的危险因素。适应性免疫反应在 MS 的发病机制中起着关键作用,其中自身反应性 T 细胞和自身抗体是主要的协调者。免疫反应受抑制分子调节,这些分子调节适应性系统的激活和止血界面。这些分子通过抑制细胞因子分泌和 T 细胞增殖来抑制免疫反应,从而减少炎症和相应的损伤。因此,抑制分子在调节健康和安全的免疫反应中的关键作用使它们成为免疫治疗的极具吸引力的靶点。在这篇综述论文中,将总结在多发性硬化症发病机制和实验性自身免疫性脑脊髓炎(EAE)动物模型中表达的各种免疫细胞类型上的抑制分子的作用。