Cohen Jeffrey A
Mellen Center for Multiple Sclerosis Treatment and Research, Cleveland Clinic Foundation, Cleveland, OH, USA.
J Neurol Sci. 2009 Feb 1;277 Suppl 1:S55-61. doi: 10.1016/S0022-510X(09)70015-2.
Recent years have seen considerable evolution and increasing sophistication of our concepts of the pathophysiology of multiple sclerosis. These new notions include the increased recognition of the importance of extralesional pathology, of the interplay between inflammation and neurodegenerative changes, pathophysiological heterogeneity and additional immune cell populations contributing to disease. These advances have driven the development and evaluation of new therapeutic strategies and outcome measures for clinical trials. A sizeable number of new immunomodulatory and immunosuppressive agents are under development and attracting great attention. These may offer potential advantages over existing treatments in terms of convenience and efficacy, but certain agents may raise safety concerns. In addition, neuroprotective and repair strategies are beginning to be considered. Not all of these agents will eventually be marketed but they will all help us gain insight into the pathophysiology of multiple sclerosis and decipher the mechanisms that underlie its heterogeneity. The place that these therapies will come to occupy in future years will depend on their relative benefits and risks.
近年来,我们对多发性硬化症病理生理学的概念有了相当大的演变,并且日益复杂。这些新观念包括对病灶外病理学重要性的更多认识、炎症与神经退行性变之间的相互作用、病理生理异质性以及促成疾病的其他免疫细胞群体。这些进展推动了临床试验中新治疗策略和疗效指标的开发与评估。大量新型免疫调节和免疫抑制药物正在研发中,并备受关注。就便利性和疗效而言,这些药物可能比现有治疗方法具有潜在优势,但某些药物可能引发安全问题。此外,神经保护和修复策略也开始受到关注。并非所有这些药物最终都会上市,但它们都将帮助我们深入了解多发性硬化症的病理生理学,并破解其异质性背后的机制。这些疗法在未来几年所占据的地位将取决于它们相对的益处和风险。