Department of Neurology, University of Michigan, 4013 Biomedical Science Research Building, 109 Zina Pitcher Place, SPC 2200, Ann Arbor, MI, 48109, USA.
Curr Treat Options Neurol. 2013 Jun;15(3):259-69. doi: 10.1007/s11940-013-0232-y.
The aims of this article are to discuss the potential role of B lymphocytes in the pathogenesis of multiple sclerosis (MS) and in the mechanisms of action of approved and emerging disease modifying therapies. Over the last few years, significant progress has been made in the introduction of novel pharmacologic treatments that reduce the frequency of clinical exacerbations and radiological lesion formation in relapsing remitting MS. The mechanisms of action of a number of these disease modifying therapies (DMT) implicate B cells in the pathogenesis, as well as in the regulation, of MS. Further research into B-cell subset trafficking patterns, functional activities and interactions with other immune cells in the context of neuroinflammation is likely to inform the development of future generations of DMT.
本文旨在探讨 B 淋巴细胞在多发性硬化症(MS)发病机制中的潜在作用,以及已批准和新兴的疾病修正治疗方法的作用机制。在过去的几年中,在引入新型药物治疗方面取得了重大进展,这些治疗方法可降低复发缓解型 MS 患者的临床恶化和放射学损伤形成频率。许多这些疾病修正治疗(DMT)的作用机制表明,B 细胞在 MS 的发病机制以及调节中起作用。进一步研究 B 细胞亚群在神经炎症背景下的迁移模式、功能活性和与其他免疫细胞的相互作用,可能为新一代 DMT 的开发提供信息。