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Autoimmunity in Amyotrophic Lateral Sclerosis: Past and Present

机译:肌萎缩性侧索硬化的自身免疫:过去和现在

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Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease affecting particularly motor neurons for which no cure or effective treatment is available. Although the cause of ALS remains unknown, accumulative evidence suggests an autoimmune mechanism of pathogenesis. In this paper, we will summarize the current research related to autoimmunity in the sporadic form of ALS and discuss the potential underlying pathogenic mechanisms and perspectives. Presented data supports the view that humoral immune responses against motor nerve terminals can initiate a series of physiological changes leading to alteration of calcium homeostasis. In turn, loss of calcium homeostasis may induce neuronal death through apoptotic signaling pathways. Additional approaches identifying specific molecular features of this hypothesis are required, which will hopefully allow us to develop techniques of early diagnosis and effective therapies.
机译:肌萎缩性侧索硬化症(ALS)是一种致命的神经退行性疾病,特别是影响运动神经元的致命神经退行性疾病,目前尚无治愈或有效治疗方法。尽管ALS的病因尚不清楚,但累积的证据表明发病机制是自身免疫机制。在本文中,我们将总结目前以散发性ALS形式进行的与自身免疫有关的研究,并讨论潜在的潜在致病机制和观点。提出的数据支持这样的观点,即针对运动神经末梢的体液免疫反应可以引发一系列生理变化,从而导致钙稳态的改变。反过来,钙稳态的丧失可能通过凋亡信号通路诱导神经元死亡。还需要其他方法来鉴定该假设的特定分子特征,这有望使我们能够开发早期诊断和有效疗法的技术。

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