Department of Neurology, The First Affiliated Hospital of China Medical University, Shenyang, Liao Ning Province, China.
J Neuroimmunol. 2012 Aug 15;249(1-2):16-26. doi: 10.1016/j.jneuroim.2012.04.014. Epub 2012 May 23.
To develop a safe and efficient vaccine for AD treatment, we constructed an adenovirus vector vaccine encoding ten repeats of Aβ3-10 and CpG motif as a molecular adjuvant. We demonstrated that therapeutic immunization with Ad-10×Aβ3-10-CpG elicits Aβ3-10 specific Th2-polarized immune response with high titers of anti-Aβ antibodies in APPswe/PSEN1dE9 mice, which in turn reduced Aβ deposits in brains and cognitive impairment. In addition, Ad-10×Aβ3-10-CpG reduced astrocytosis without increasing the incidence of microhemorrhage. Our findings of this study raise the possibility that the adenovirus vaccine Ad-10×Aβ3-10-CpG would be a safe and effective alternative for AD immunotherapy.
为了开发一种安全有效的 AD 治疗疫苗,我们构建了一种腺病毒载体疫苗,该疫苗编码 Aβ3-10 的十个重复序列和 CpG 基序作为分子佐剂。我们证明,用 Ad-10×Aβ3-10-CpG 进行治疗性免疫接种可在 APPswe/PSEN1dE9 小鼠中引发 Aβ3-10 特异性 Th2 极化免疫反应,并产生高滴度的抗 Aβ 抗体,从而减少大脑中的 Aβ 沉积和认知障碍。此外,Ad-10×Aβ3-10-CpG 减少了星形胶质细胞增生,而没有增加微出血的发生率。我们的研究结果表明,腺病毒疫苗 Ad-10×Aβ3-10-CpG 可能是 AD 免疫治疗的一种安全有效的替代方法。