克拉德滨片作为多发性硬化症选择性免疫重建治疗的一个关键例子的潜在作用。

Degenerative Neurological and Neuromuscular Disease Pub Date : 2018-05-03 eCollection Date: 2018-01-01 DOI:10.2147/DNND.S161450
Alexey N Boyko, Olga V Boyko
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引用次数: 16

摘要

多发性硬化症(MS)是年轻人最重要、致残和普遍的神经系统疾病之一。它是一种慢性炎症和神经退行性疾病,当自身反应性B和T细胞具有下游作用时,导致脱髓鞘和神经元丢失。抗炎疾病改善疗法在延缓多发性硬化症疾病和残疾进展方面已被证实有效。虽然多发性硬化症治疗的进展已经总体上改善了患者的预后和生活质量,但目前的多发性硬化症治疗领域仍存在一些明显的不足和未满足的需求。最有希望的MS治疗手段是选择性免疫重建疗法(SIRT)。这种疗法是在短期的免疫抑制过程中给予的,对免疫系统产生持久的影响,防止神经组织损失。这篇综述讨论了作为多发性硬化症SIRT的例子,克拉宾片的作用机制和临床试验数据。在这些研究中,克拉宾片的临床益处包括降低复发率和残疾进展,大幅减少病变活动,并防止脑容量损失。是否所有这些神经学上的发现都是淋巴细胞耗竭的直接结果,或者是否对其他未知的神经退行性过程有下游影响还有待确定,但这些都清楚地指向了一个有趣的研究领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cladribine tablets' potential role as a key example of selective immune reconstitution therapy in multiple sclerosis.

Cladribine tablets' potential role as a key example of selective immune reconstitution therapy in multiple sclerosis.

Cladribine tablets' potential role as a key example of selective immune reconstitution therapy in multiple sclerosis.

Cladribine tablets' potential role as a key example of selective immune reconstitution therapy in multiple sclerosis.

Multiple sclerosis (MS) is one of the most important, disabling, and prevalent neurological disorders of young adults. It is a chronic inflammatory and neurodegenerative disease when autoreactive B and T cells have downstream effects that result in demyelination and neuronal loss. Anti-inflammatory disease-modifying therapies do have proven efficacy in delaying disease and disability progression in MS. While the progress in MS treatments has already improved the prognosis and quality of patients' lives overall, there are some clear shortcomings and unmet needs in the current MS treatment landscape. The most promising means of MS treatment is selective immune reconstitution therapy (SIRT). This therapy is given in short-duration courses of immunosuppression, producing durable effects on the immune system and preventing nervous tissue loss. This review discusses the mechanisms of action and the data of clinical trials of cladribine tablets as an example of SIRT in MS. The clinical benefits of cladribine tablets in these studies include decreased relapse rate and disability progression with large reductions in lesion activity, and protection against brain volume loss. Whether all of these neurological findings are direct results of lymphocyte depletion, or if there are downstream effects on other, unknown, neurodegenerative processes are yet to be determined, but these clearly point to an interesting area of research.

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