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多发性硬化症的多次范式转变。

Multiple paradigm shifts in multiple sclerosis.

作者信息

Kieseier Bernd C, Hartung Hans-Peter

出版信息

Curr Opin Neurol. 2003 Jun;16(3):247-52. doi: 10.1097/01.wco.0000073923.19076.75.

Abstract

PURPOSE OF REVIEW

The present article reviews the currently ongoing scientific debate of our changing views on the pathogenesis of multiple sclerosis and the therapeutic strategies currently available for multiple sclerosis.

RECENT FINDINGS

The most important observations include that (a) axonal loss accounts for permanent disability in multiple sclerosis, (b) remyelination should be possible in theory but fails for unknown reasons in the multiple sclerosis lesion, (c) inflammation can be beneficial, (d) treatment should be initiated early, and (e) immunosuppressive strategies exhibit beneficial effects in progressive forms of the disease.

SUMMARY

Our current understanding of the immunopathogenesis of multiple sclerosis has changed in the past. Whereas demyelination was originally thought to be relevant for the lasting neurological deficit, it is nowadays commonly accepted that the extent of axonal loss dictates the degree of permanent clinical disability. How axonal damage can be prevented remains elusive. The interaction between the myelinating cell and the neuron gains increasing attention, however the evolving knowledge has not yet yielded new treatment concepts. Hence for the time being, it seems prudent to make optimal use of current approved therapies. Recent trials underlined the need for early initiation of treatment with immunomodulatory drugs. The superiority of one of the interferons is still a matter of debate, and a conclusive answer cannot be given at present. Finally, with mitoxantrone we have a drug at hand which can be used in progressive forms of multiple sclerosis, especially when other disease modifying drugs are not or no longer effective.

摘要

综述目的

本文综述了当前正在进行的关于我们对多发性硬化症发病机制不断变化的观点以及目前可用于多发性硬化症的治疗策略的科学辩论。

最新发现

最重要的观察结果包括:(a)轴突损失导致多发性硬化症的永久性残疾;(b)理论上髓鞘再生应该是可行的,但在多发性硬化症病变中由于未知原因而失败;(c)炎症可能有益;(d)治疗应尽早开始;(e)免疫抑制策略对疾病的进展形式显示出有益效果。

总结

我们目前对多发性硬化症免疫发病机制的理解在过去已经发生了变化。虽然脱髓鞘最初被认为与持久的神经功能缺损有关,但如今人们普遍认为轴突损失的程度决定了永久性临床残疾的程度。如何预防轴突损伤仍然不清楚。髓鞘形成细胞与神经元之间的相互作用越来越受到关注,然而不断发展的知识尚未产生新的治疗概念。因此,目前明智的做法似乎是充分利用当前已获批的疗法。最近的试验强调了尽早开始使用免疫调节药物治疗的必要性。其中一种干扰素的优越性仍然存在争议,目前无法给出确凿答案。最后,我们手头有一种药物米托蒽醌,可用于多发性硬化症的进展形式,特别是当其他疾病修正药物无效或不再有效时。

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