Kassis Ibrahim, Ben-Zwi Moriel, Petrou Panayiota, Halimi Michele, Karussis Dimitrios
Unit of Neuroimmunology and Multiple Sclerosis Center, Hadassah University Hospital, Jerusalem, Ein-Kerem, Israel.
Unit of Neuroimmunology and Multiple Sclerosis Center, Hadassah University Hospital, Jerusalem, Ein-Kerem, Israel.
Immunol Lett. 2021 May;233:11-19. doi: 10.1016/j.imlet.2021.03.003. Epub 2021 Mar 4.
Fingolimod (Gilenya™) is an effective oral medication approved for relapsing-remitting multiple sclerosis (MS), albeit less effective in chronic disease. Its main mechanism of action is through peripheral immunomodulation but neuroprotective effects may also be involved. Mesenchymal stem cells (MSC) were shown to exert immunomodulatory and neurotrophic effects in the model of multiple sclerosis (experimental autoimmune encephalomyelitis-EAE). The use of combination treatments in chronic diseases such as MS, has long been advocated and may result in improvement of the beneficial effects of each one of them. We tested the in vitro effects of Fingolimod (FTY720) on MSC and the in vivo effect of such combination treatment in the model of EAE. Fingolimod did not affect in any detrimental way the basic features of MSCs and it promoted their migration and proliferation ability .Moreover, Fingolimod induced neurotrophic factors secretion and suppressed the production of pro-inflammatory cytokines from astrocytes and microglia, in vitro. In vivo, the combined treatment of FTY720 and MSC (either by the intravenous or the intra-cerebroventricular route of administration) resulted in synergistic clinical beneficial effects compared to FTY720 or MSC alone, paralleled by a significant reduction of inflammatory CNS infiltrations and of axonal loss. These data may indicate a synergism of fingolimod with MSC and may support future combinations of immunomodulatory drugs with cellular therapies for the improvement of the benefits in progressive forms of MS.
芬戈莫德(Gilenya™)是一种获批用于复发缓解型多发性硬化症(MS)的有效口服药物,尽管在治疗慢性病方面效果较差。其主要作用机制是通过外周免疫调节,但也可能涉及神经保护作用。间充质干细胞(MSC)在多发性硬化症模型(实验性自身免疫性脑脊髓炎-EAE)中显示出免疫调节和神经营养作用。长期以来,人们一直主张在MS等慢性疾病中使用联合治疗,这可能会提高每种治疗方法的有益效果。我们测试了芬戈莫德(FTY720)对MSC的体外作用以及这种联合治疗在EAE模型中的体内作用。芬戈莫德并未以任何有害方式影响MSC的基本特征,反而促进了它们的迁移和增殖能力。此外,在体外,芬戈莫德诱导神经营养因子分泌,并抑制星形胶质细胞和小胶质细胞促炎细胞因子的产生。在体内,与单独使用FTY720或MSC相比,FTY720和MSC联合治疗(通过静脉注射或脑室内给药途径)产生了协同的临床有益效果,同时显著减少了中枢神经系统的炎症浸润和轴突损失。这些数据可能表明芬戈莫德与MSC具有协同作用,并可能支持未来免疫调节药物与细胞疗法联合使用,以改善进展型MS的治疗效果。