Friedland R P, Majocha R E, Reno J M, Lyle L R, Marotta C A
Department of Neurology, Case Western Reserve University, Cleveland, OH 44106.
Mol Neurobiol. 1994 Aug-Dec;9(1-3):107-13. doi: 10.1007/BF02816109.
We evaluated the efficacy of murine monoclonal antibodies (MAbs) targeted to the A beta amyloid of Alzheimer's disease for development of procedures for the in vivo identification of amyloid angiopathy (AA). MAbs to A beta were prepared and screened for effectiveness in visualizing AA and neuritic plaques in postmortem AD brain sections. They were assessed again after enzymatic cleavage to produce Fab fragments and after labeling with technetium-99m (99mTc) using a diamide dimercaptide ligand system. Modified and radiolabeled Fab fragments retained activity and specificity toward amyloid-laden blood vessels and neuritic plaques. A highly specific murine MAb, 10H3, was identified and characterized that fulfills criteria necessary for the development of an in vivo diagnostic imaging agent. Toxicity studies in rats showed the MAb to be safe. Biodistribution studies in mice demonstrated desirable properties for use as an imaging agent. Expansion and adaptation of these strategies may provide the methods and materials for the noninvasive analysis of AA in living patients, and permit assessment of the contribution of AA to the clinical and pathological features of AD.
我们评估了靶向阿尔茨海默病β淀粉样蛋白的鼠单克隆抗体(MAb)在开发体内识别淀粉样血管病(AA)方法方面的功效。制备了针对β淀粉样蛋白的单克隆抗体,并在死后AD脑切片中检测其在可视化AA和神经炎性斑块方面的有效性。在酶切产生Fab片段后以及使用二酰胺二巯基配体系统用99m锝(99mTc)标记后,再次对它们进行评估。修饰和放射性标记的Fab片段对富含淀粉样蛋白的血管和神经炎性斑块保持活性和特异性。鉴定并表征了一种高度特异性的鼠单克隆抗体10H3,其满足开发体内诊断成像剂所需的标准。大鼠毒性研究表明该单克隆抗体是安全的。小鼠体内分布研究证明其具有作为成像剂的理想特性。扩展和应用这些策略可能为活体患者AA的无创分析提供方法和材料,并允许评估AA对AD临床和病理特征的贡献。