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Prophylaxis and Treatment of Alzheimers Disease by Delivery of an Adeno-Associated Virus Encoding a Monoclonal Antibody Targeting the Amyloid Beta Protein

机译:预防和治疗阿尔茨海默氏病通过传递腺相关病毒编码靶向淀粉样β蛋白的单克隆抗体。

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摘要

We previously reported on a monoclonal antibody (mAb) that targeted amyloid beta (Aß) protein. Repeated injection of that mAb reduced the accumulation of Aß protein in the brain of human Aß transgenic mice (Tg2576). In the present study, cDNA encoding the heavy and light chains of this mAb were subcloned into an adeno-associated virus type 1 (AAV) vector with a 2A/furin adapter. A single intramuscular injection of 3.0×1010 viral genome of these AAV vectors into C57BL/6 mice generated serum anti-Aß Ab levels up to 0.3 mg/ml. Anti-Aß Ab levels in excess of 0.1 mg/ml were maintained for up to 64 weeks. The effect of AAV administration on Aß levels in vivo was examined. A significant decrease in Aß levels in the brain of Tg2576 mice treated at 5 months (prophylactic) or 10 months (therapeutic) of age was observed. These results support the use of AAV vector encoding anti-Aß Ab for the prevention and treatment of Alzheimer's disease.
机译:我们先前曾报道过针对淀粉样β(Aß)蛋白的单克隆抗体(mAb)。重复注射该mAb可减少人Aß转基因小鼠(Tg2576)脑内Aß蛋白的积累。在本研究中,将编码此mAb重链和轻链的cDNA亚克隆到带有2A /弗林蛋白酶衔接子的腺相关病毒1型(AAV)载体中。将这些AAV载体的3.0×10 10 病毒基因组单次肌肉注射到C57BL / 6小鼠中,产生的血清抗AßAb水平高达0.3 mg / ml。超过0.1 mg / ml的抗AßAb水平维持长达64周。检查了AAV给药对体内Aß水平的影响。观察到在治疗5个月(预防性)或10个月(治疗性)的Tg2576小鼠的大脑中Aß水平显着降低。这些结果支持使用编码抗AßAb的AAV载体预防和治疗阿尔茨海默氏病。

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