Weinstock-Guttman Bianca, Bakshi Rohit
Baird MS Research Center of The Jacobs Neurological Institute, Buffalo, New York 14203, USA.
CNS Drugs. 2004;18(12):777-92. doi: 10.2165/00023210-200418120-00003.
Multiple sclerosis (MS) is an inflammatory autoimmune disease characterised by demyelination and axonal loss in the CNS. Although new immunomodulatory therapies including interferon-beta and glatiramer acetate became available during the last decade, these therapies are only partially effective. There is a continuing need to develop more effective treatment strategies to combat the chronic and progressive aspects of the disease. In view of the complex pathophysiology underlying the MS disease process, combination therapy offers a rational therapeutic approach. Combining immunomodulatory agents with different mechanisms of action that promote synergistic or additive effects represents an important objective in MS therapeutic research. Ultimately, the optimal therapies will likely include strategies that promote repair and limit tissue destruction in combination with anti-inflammatory interventions.
多发性硬化症(MS)是一种炎症性自身免疫疾病,其特征是中枢神经系统(CNS)发生脱髓鞘和轴突损失。尽管在过去十年间出现了包括β-干扰素和醋酸格拉替雷在内的新型免疫调节疗法,但这些疗法仅部分有效。持续需要开发更有效的治疗策略来对抗该疾病的慢性和进行性方面。鉴于MS疾病进程背后复杂的病理生理学,联合治疗提供了一种合理的治疗方法。将具有促进协同或累加效应的不同作用机制的免疫调节药物联合起来是MS治疗研究中的一个重要目标。最终,最佳疗法可能会包括促进修复和限制组织破坏的策略,并结合抗炎干预措施。