Department of Microbiology and Immunology, The University of British Columbia, Vancouver, BC, Canada.
Department of Health and Human Performance, Texas State University, San Marcos, TX, USA.
Mult Scler. 2022 Jan;28(1):29-48. doi: 10.1177/13524585211008760. Epub 2021 Apr 19.
Immune-mediated demyelination and consequent degeneration of oligodendrocytes and axons are hallmark features of multiple sclerosis (MS). Remyelination declines in progressive MS, causing permanent axonal loss and irreversible disabilities. Strategies aimed at enhancing remyelination are critical to attenuate disease progression.
We systematically reviewed recent advances in neuroprotective and regenerative therapies for MS, covering preclinical and clinical studies.
We searched three biomedical databases using defined keywords. Two authors independently reviewed articles for inclusion based on pre-specified criteria. The data were extracted from each study and assessed for risk of bias.
Our search identified 7351 studies from 2014 to 2020, of which 221 met the defined criteria. These studies reported 262 interventions, wherein 92% were evaluated in animal models. These interventions comprised protein, RNA, lipid and cellular biologics, small molecules, inorganic compounds, and dietary and physiological interventions. Small molecules were the most highly represented strategy, followed by antibody therapies and stem cell transplantation.
While significant strides have been made to develop regenerative treatments for MS, the current evidence illustrates a skewed representation of the types of strategies that advance to clinical trials. Further examination is thus required to address current barriers to implementing experimental treatments in clinical settings.
免疫介导的脱髓鞘以及随之而来的少突胶质细胞和轴突变性是多发性硬化症(MS)的标志性特征。进行性 MS 中的髓鞘再生能力下降,导致轴突永久性丢失和不可逆转的残疾。旨在增强髓鞘再生的策略对于减轻疾病进展至关重要。
我们系统地回顾了多发性硬化症神经保护和再生治疗的最新进展,涵盖了临床前和临床研究。
我们使用定义的关键词在三个生物医学数据库中进行了搜索。两名作者根据预先规定的标准独立审查文章是否纳入。从每项研究中提取数据,并评估其偏倚风险。
我们的搜索从 2014 年到 2020 年确定了 7351 项研究,其中 221 项符合既定标准。这些研究报告了 262 种干预措施,其中 92%是在动物模型中进行评估的。这些干预措施包括蛋白质、RNA、脂质和细胞生物制剂、小分子、无机化合物、饮食和生理干预。小分子是最具代表性的策略,其次是抗体疗法和干细胞移植。
尽管在开发多发性硬化症再生治疗方面已经取得了重大进展,但目前的证据表明,推进临床试验的策略类型存在明显的偏向。因此,需要进一步研究来解决当前在临床环境中实施实验性治疗的障碍。