Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Department of Neurology and Neurotherapeutics, Clinical Center for Multiple Sclerosis, Multiple Sclerosis and Neuroimmunology Imaging Program, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Neurotherapeutics. 2016 Jan;13(1):58-69. doi: 10.1007/s13311-015-0409-z.
Identifying effective therapies for the treatment of progressive forms of multiple sclerosis (MS) is a highly relevant priority and one of the greatest challenges for the global MS community. Better understanding of the mechanisms involved in progression of the disease, novel trial designs, drug repurposing strategies, and new models of collaboration may assist in identifying effective therapies. In this review, we discuss various therapies under study in phase II or III trials, including antioxidants (idebenone); tyrosine kinase inhibitors (masitinib); sphingosine receptor modulators (siponimod); monoclonal antibodies (anti-leucine-rich repeat and immunoglobulin-like domain containing neurite outgrowth inhibitor receptor-interacting protein-1, natalizumab, ocrelizumab, intrathecal rituximab); hematopoetic stem cell therapy; statins and other possible neuroprotective agents (amiloride, riluzole, fluoxetine, oxcarbazepine); lithium; phosphodiesterase inhibitors (ibudilast); hormone-based therapies (adrenocorticotrophic hormone and erythropoietin); T-cell receptor peptide vaccine (NeuroVax); autologous T-cell immunotherapy (Tcelna); MIS416 (a microparticulate immune response modifier); dopamine antagonists (domperidone); and nutritional supplements, including lipoic acid, biotin, and sunphenon epigallocatechin-3-gallate (green tea extract). Given ongoing and planned clinical trial initiatives, and the largest ever focus of the global research community on progressive MS, future prospects for developing targeted therapeutics aimed at reducing disability in progressive forms of MS appear promising.
确定治疗多发性硬化症(MS)进行性形式的有效疗法是一个高度相关的优先事项,也是全球 MS 社区面临的最大挑战之一。更好地了解疾病进展所涉及的机制、新的试验设计、药物再利用策略以及新的合作模式,可能有助于确定有效的治疗方法。在这篇综述中,我们讨论了正在进行的 II 期或 III 期临床试验中的各种疗法,包括抗氧化剂(依地醌);酪氨酸激酶抑制剂(马替斯替尼);鞘氨醇受体调节剂(西尼莫德);单克隆抗体(抗亮氨酸丰富重复和免疫球蛋白样结构域包含神经突生长抑制因子受体相互作用蛋白-1、那他珠单抗、奥瑞珠单抗、鞘内利妥昔单抗);造血干细胞治疗;他汀类药物和其他可能的神经保护剂(阿米洛利、利鲁唑、氟西汀、奥卡西平);锂;磷酸二酯酶抑制剂(伊布地尔);基于激素的疗法(促肾上腺皮质激素和促红细胞生成素);T 细胞受体肽疫苗(NeuroVax);自体 T 细胞免疫疗法(Tcelna);MIS416(一种微粒免疫反应调节剂);多巴胺拮抗剂(多潘立酮);以及营养补充剂,包括硫辛酸、生物素和银杏叶多酚 EGCG(绿茶提取物)。鉴于正在进行和计划中的临床试验计划,以及全球研究界对进行性 MS 的最大关注,未来开发针对进行性 MS 的靶向治疗药物以减少残疾的前景似乎很有希望。