通过β淀粉样蛋白口服疫苗治疗阿尔茨海默病的新策略

Y. Matsuzaka, R. Yashiro
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引用次数: 0

摘要

阿尔茨海默病(AD)是一种以进行性认知障碍和痴呆为特征的神经病理学。该疾病归因于老年斑块,老年斑块是神经细胞外淀粉样蛋白β(Aβ)的聚集体;神经原纤维缠结,是神经细胞中磷酸化tau的丝状积聚;以及脑组织中神经元的丧失。用Aβ免疫AD小鼠模型可以消除先前存在的老年斑块淀粉样蛋白,并防止新的淀粉样蛋白积聚。此外,其效果表明,被动免疫可以改善认知功能,而没有副作用,如疫苗治疗AD模型小鼠的淋巴细胞浸润,这表明疫苗治疗AD的可能性。此外,考虑到直接给药Aβ可能产生副作用,安全口服疫苗的实际应用,在植物中表达Aβ。事实上,阿尔茨海默病模型小鼠口服这种疫苗减少了Aβ在大脑中的积累。此外,几乎没有观察到炎性IgG的表达。因此,在Aβ积累之前或在积累的早期接种疫苗可以防止Aβ引起AD。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel Strategy for Alzheimer’s Disease Treatment through Oral Vaccine Therapy with Amyloid Beta
Alzheimer’s disease (AD) is a neuropathology characterized by progressive cognitive impairment and dementia. The disease is attributed to senile plaques, which are aggregates of amyloid beta (Aβ) outside nerve cells; neurofibrillary tangles, which are filamentous accumulations of phosphorylated tau in nerve cells; and loss of neurons in the brain tissue. Immunization of an AD mouse model with Aβ-eliminated pre-existing senile plaque amyloids and prevented new accumulation. Furthermore, its effect showed that cognitive function can be improved by passive immunity without side effects, such as lymphocyte infiltration in AD model mice treated with vaccine therapy, indicating the possibility of vaccine therapy for AD. Further, considering the possibility of side effects due to direct administration of Aβ, the practical use of the safe oral vaccine, which expressed Aβ in plants, is expected. Indeed, administration of this oral vaccine to Alzheimer’s model mice reduced Aβ accumulation in the brain. Moreover, almost no expression of inflammatory IgG was observed. Therefore, vaccination prior to Aβ accumulation or at an early stage of accumulation may prevent Aβ from causing AD.
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