首页> 外文期刊>Neurochemical research >In vivo electroporation of a new gene vaccine encoding ten repeats of aβ3-10 prevents brain aβ deposition and delays cognitive impairment in Young Tg-APPswe/PSEN1dE9 Mice
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In vivo electroporation of a new gene vaccine encoding ten repeats of aβ3-10 prevents brain aβ deposition and delays cognitive impairment in Young Tg-APPswe/PSEN1dE9 Mice

机译:编码10个重复的aβ3-10的新基因疫苗的体内电穿孔可防止幼小Tg-APPswe / PSEN1dE9小鼠大脑aβ沉积并延缓认知障碍

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Active immunization holds great promise for the treatment of Alzheimer's disease but the infiltration of T-lymphocytes and associated meningoencephalitis observed in clinical trials needs to be overcome. To avoid this toxicity, previous studies have used synthetic truncated derivatives of Ab to promote humoral immunity. In this study, we developed a novel vaccine [p(Ab3-10)10-MT] that expresses ten repeats of Ab3-10 with melatonin (MT) as an adjuvant, and administered it intramuscularly in three-month-old Tg-APPswe/PSEN1dE9 (Tg) mice by in vivo electroporation. The p(Ab3-10)10-MT vaccine induced high titers of anti-Ab antibodies, which in turn reduced Ab deposits in the mouse brains and decreased cognitive impairment. Immunoglobulin isotyping revealed a predominantly IgG1 response, indicating a Th2 antiinflammatory response. Ex vivo cultured splenocytes exhibited a low IFN-c and high IL-4 response. Immunohistochemical analysis revealed that glial cell activation was also attenuated. These results indicate that p(Ab3- 10)10-MT may potentially be an effective vaccine to reduce accumulated Ab and attenuate cognitive deficits.
机译:主动免疫疗法有望治疗阿尔茨海默氏病,但需要克服临床试验中观察到的T淋巴细胞浸润和相关的脑膜脑炎。为了避免这种毒性,以前的研究已使用合成的Ab的截短衍生物来促进体液免疫。在这项研究中,我们开发了一种新型疫苗[p(Ab3-10)10-MT],该疫苗以褪黑激素(MT)作为佐剂表达Ab3-10的10个重复序列,并在三个月大的Tg-APPswe中肌肉注射/ PSEN1dE9(Tg)小鼠体内电穿孔。 p(Ab3-10)10-MT疫苗诱导出高滴度的抗Ab抗体,从而减少了小鼠脑中的Ab沉积并减少了认知障碍。免疫球蛋白分型显示主要是IgG1反应,表明Th2抗炎反应。离体培养的脾细胞表现出低IFN-c和高IL-4应答。免疫组织化学分析显示神经胶质细胞活化也减弱。这些结果表明,p(Ab3-10)10-MT可能是减少累积的Ab和减轻认知缺陷的有效疫苗。

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