Division of Neurology, Department of Medicine, St. Michael's Hospital, University of Toronto, Ontario, Canada.
Department of Neurology, Johns Hopkins University, Baltimore, MD, USA.
Nat Rev Neurol. 2022 Aug;18(8):466-475. doi: 10.1038/s41582-022-00675-0. Epub 2022 Jun 13.
The rapidly evolving therapeutic landscape of multiple sclerosis (MS) has contributed to paradigm shifts in our understanding of the biological mechanisms that contribute to CNS injury and in treatment philosophies. Opportunities remain to further improve treatment of relapsing-remitting MS, but two major therapeutic gaps are the limiting of progressive disease mechanisms and the repair of CNS injury. In this Review, we provide an overview of selected emerging therapies that predominantly target processes within the CNS that are thought to be involved in limiting non-relapsing, progressive disease injury or promoting tissue repair. Among these, we consider agents that modulate adaptive and innate CNS-compartmentalized inflammation, which can be mediated by infiltrating immune cells and/or resident CNS cells, including microglia and astrocytes. We also discuss agents that target degenerative disease mechanisms, agents that might confer neuroprotection, and agents that create a more favourable environment for or actively contribute to oligodendrocyte precursor cell differentiation, remyelination and axonal regeneration. We focus on agents that are novel for MS, that are known to or are presumed to penetrate the CNS, and that have already entered early stages of development in MS clinical trials.
多发性硬化症(MS)的治疗领域迅速发展,促使我们对导致中枢神经系统损伤的生物学机制以及治疗理念的认识发生了转变。目前仍然有机会进一步改善复发缓解型 MS 的治疗,但有两个主要的治疗空白,即限制进行性疾病机制和中枢神经系统损伤的修复。在这篇综述中,我们概述了一些选定的新兴疗法,这些疗法主要针对被认为参与限制非复发、进行性疾病损伤或促进组织修复的中枢神经系统内的过程。在这些疗法中,我们考虑了调节适应性和固有中枢神经系统局部炎症的药物,这些炎症可以由浸润的免疫细胞和/或中枢神经系统的固有细胞(包括小胶质细胞和星形胶质细胞)介导。我们还讨论了针对退行性疾病机制的药物、可能具有神经保护作用的药物,以及为少突胶质细胞前体细胞分化、髓鞘再生和轴突再生创造更有利环境或积极做出贡献的药物。我们重点关注那些针对 MS 的新型药物,这些药物已知或推测能够穿透中枢神经系统,并且已经在 MS 的临床试验中进入早期开发阶段。