Chandran Siddharthan, Hunt David, Joannides Alexis, Zhao Chao, Compston Alastair, Franklin Robin J M
Cambridge Centre for Brain Repair, University of Cambridge, Robinson Way, Cambridge CB2 2PY, UK.
Philos Trans R Soc Lond B Biol Sci. 2008 Jan 12;363(1489):171-83. doi: 10.1098/rstb.2006.2019.
Multiple sclerosis is the most common potential cause of neurological disability in young adults. The disease has two distinct clinical phases, each reflecting a dominant role for separate pathological processes: inflammation drives activity during the relapsing-remitting stage and axon degeneration represents the principal substrate of progressive disability. Recent advances in disease-modifying treatments target only the inflammatory process. They are ineffective in the progressive stage, leaving the science of disease progression unsolved. Here, the requirement is for strategies that promote remyelination and prevent axonal loss. Pathological and experimental studies suggest that these processes are tightly linked, and that remyelination or myelin repair will both restore structure and protect axons. This review considers the basic and clinical biology of remyelination and the potential contribution of stem and precursor cells to enhance and supplement spontaneous remyelination.
多发性硬化症是年轻成年人神经功能障碍最常见的潜在病因。该疾病有两个不同的临床阶段,每个阶段都反映了不同病理过程的主导作用:在复发缓解期,炎症驱动疾病活动,而轴突退变是进行性残疾的主要基础。疾病修正治疗的最新进展仅针对炎症过程。它们在疾病进展阶段无效,使得疾病进展的科学问题仍未解决。在此,需要促进髓鞘再生和预防轴突丢失的策略。病理和实验研究表明,这些过程紧密相连,髓鞘再生或髓鞘修复既能恢复结构又能保护轴突。本综述探讨了髓鞘再生的基础和临床生物学,以及干细胞和前体细胞在增强和补充自然髓鞘再生方面的潜在作用。