Rice Claire, Halfpenny Christopher, Scolding Neil
University of Bristol Institute of Clinical Neurosciences, Department of Neurology, Frenchay Hospital, Bristol, BS16 1LE, United Kingdom.
NeuroRx. 2004 Oct;1(4):415-23. doi: 10.1602/neurorx.1.4.415.
Multiple sclerosis presents particular and serious problems to those attempting to develop cell-based therapies: the occurrence of innumerable lesions scattered throughout the CNS, axon loss, astrocytosis, and a continuing inflammatory process, to name but a few. Nevertheless, the limited and relatively focused nature of damage to oligodendrocytes and myelin, at least in early disease, the large body of available knowledge concerning the biology of oligodendrocytes, and the success of experimental myelin repair, have allowed cautious optimism that therapies may be possible. Here, we review the clinical and biological problems presented by multiple sclerosis in the context of cell therapies, and the neuroscientific background to the development of strategies for myelin repair. We attempt to highlight those areas where difficulties have yet to be resolved and draw on a variety of more recent experimental findings to speculate on how remyelinating therapies are likely to develop in the foreseeable future.
无数病变散布于整个中枢神经系统、轴突损失、星形细胞增生以及持续的炎症过程等等。然而,少突胶质细胞和髓鞘损伤的局限性和相对集中性,至少在疾病早期如此,大量关于少突胶质细胞生物学的现有知识,以及实验性髓鞘修复的成功,使人们谨慎乐观地认为治疗或许可行。在此,我们在细胞疗法的背景下审视多发性硬化症所呈现的临床和生物学问题,以及髓鞘修复策略发展的神经科学背景。我们试图突出那些尚未解决的难题领域,并借鉴各种最新实验结果来推测在可预见的未来髓鞘再生疗法可能如何发展。