Okura Yoshio, Matsumoto Yoh
Department of Molecular Neuropathology, Tokyo Metropolitan Institute for Neuroscience, Fuchu, Tokyo, Japan.
Rejuvenation Res. 2008 Apr;11(2):301-8. doi: 10.1089/rej.2007.0638.
Alzheimer's disease is the most common cause of dementia characterized by progressive neurodegeneration. Based on the amyloid cascade hypothesis, a vaccine therapy for Alzheimer's disease (AD) was developed as a curative treatment. In 1999, the amyloid beta (Abeta) reduction in AD model transgenic mice with active vaccination with Abeta peptide was first reported. Although the clinical trials of active vaccination for AD patients were halted due to the development of meningoencephalitis in some patients, from the analysis of the clinical and pathological findings of treated patients, the vaccine therapy is thought to be effective. Based on such information, the vaccines for clinical application of human AD have been improved to control excessive immune reaction. Recently, we have developed non-viral DNA vaccines and obtained substantial Abeta reduction in transgenic mice without side effects. DNA vaccines have many advantages over conventional active or passive immunization. In this article, we review conventional vaccine therapies and further explain our non-viral DNA vaccine therapy. Finally, we show some data regarding the mechanisms of Abeta reduction after administration of DNA vaccines. DNA vaccination may open up new avenues of vaccine therapy for AD.
阿尔茨海默病是痴呆最常见的病因,其特征为进行性神经退行性变。基于淀粉样蛋白级联假说,开发了一种用于治疗阿尔茨海默病(AD)的疫苗疗法。1999年,首次报道了用β淀粉样蛋白(Aβ)肽主动免疫的AD模型转基因小鼠中Aβ减少的情况。尽管由于部分患者发生了脑膜脑炎,AD患者主动免疫的临床试验被中止,但从对治疗患者的临床和病理结果分析来看,疫苗疗法被认为是有效的。基于这些信息,用于人类AD临床应用的疫苗已得到改进,以控制过度的免疫反应。最近,我们开发了非病毒DNA疫苗,并在转基因小鼠中实现了显著的Aβ减少且无副作用。与传统的主动或被动免疫相比,DNA疫苗具有许多优势。在本文中,我们回顾了传统疫苗疗法,并进一步阐述了我们的非病毒DNA疫苗疗法。最后,我们展示了一些关于DNA疫苗接种后Aβ减少机制的数据。DNA疫苗接种可能为AD疫苗疗法开辟新途径。