Department of Molecular Biodefense Research, Yokohama City University, Yokohama, Kanagawa, Japan.
PLoS One. 2013;8(3):e57606. doi: 10.1371/journal.pone.0057606. Epub 2013 Mar 28.
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 3.0×10(10) 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.
我们之前曾报道过一种针对淀粉样蛋白β(Aβ)蛋白的单克隆抗体(mAb)。该 mAb 的重复注射可减少人 Aβ转基因小鼠(Tg2576)脑内 Aβ蛋白的积累。在本研究中,该 mAb 的重链和轻链的 cDNA 被亚克隆到腺相关病毒 1 型(AAV)载体中,带有 2A/弗林蛋白酶接头。将这些 AAV 载体的 3.0×10(10)个病毒基因组单次肌肉内注射到 C57BL/6 小鼠中,可使血清抗 Aβ Ab 水平高达 0.3 mg/ml。超过 0.1 mg/ml 的抗 Aβ Ab 水平可维持长达 64 周。还研究了 AAV 给药对体内 Aβ水平的影响。在 5 个月(预防性)或 10 个月(治疗性)龄时治疗的 Tg2576 小鼠脑内 Aβ水平显著降低。这些结果支持使用编码抗 Aβ Ab 的 AAV 载体用于预防和治疗阿尔茨海默病。