1 The Center for Neurologic Diseases, Brigham and Women's Hospital and Harvard Medical School , Boston, Massachusetts.
Rejuvenation Res. 2014 Apr;17(2):97-104. doi: 10.1089/rej.2013.1524.
Amyloidosis involves the extracellular deposition of proteinaceous amyloid fibrils and accessory molecules in organ(s) and/or tissue(s), and is associated with a host of human diseases, including Alzheimer disease, diabetes, and heart disease. Unfortunately, the amyloidoses are currently incurable, and there is an urgent need for less invasive diagnostics. To address this, we have generated 22 monoclonal antibodies (mAbs) against aggregates formed by a blood transport protein, transthyretin (TTR), which primarily forms amyloid fibrils in a patient's heart and/or peripheral nerves. Four of the mAbs, 2T5C9, 2G9C, T1F11, and TB2H7, demonstrated diagnostic potential in enzyme-linked immunosorbent assays (ELISA) by their low to sub-nanomolar cross-reactivity with recombinant wild-type (WT) and mutant TTR aggregates and lack of binding to native TTR or amyloid fibrils formed by other peptides or proteins. Notably, in the presence of normal human sera, three of the four mAbs, 2T5C9, 2G9C, and T1F11, retained low nM binding to TTR amyloid fibrils derived from two patients with familial amyloidotic polyneuropathy (FAP). The two most promising mAbs, 2T5C9 and 2G9C, were also shown by immunohistochemistry to have low nM binding to TTR amyloid deposits in cardiac tissue sections from two FAP patients. Taken together, these findings strongly support further investigations on the diagnostic utility of TTR aggregate specific mAbs for patients with TTR amyloidoses.
淀粉样变性涉及蛋白质样淀粉样纤维和附属分子在器官和/或组织中的细胞外沉积,与许多人类疾病有关,包括阿尔茨海默病、糖尿病和心脏病。不幸的是,淀粉样变性目前无法治愈,迫切需要更具侵入性的诊断方法。为了解决这个问题,我们生成了 22 种针对血液转运蛋白转甲状腺素蛋白(TTR)形成的聚集体的单克隆抗体(mAbs),TTR 在患者的心脏和/或外周神经中主要形成淀粉样纤维。其中 4 种 mAbs,2T5C9、2G9C、T1F11 和 TB2H7,在酶联免疫吸附测定(ELISA)中通过其与重组野生型(WT)和突变型 TTR 聚集体的低至亚纳摩尔的交叉反应性和缺乏与天然 TTR 或由其他肽或蛋白质形成的淀粉样纤维的结合显示出诊断潜力。值得注意的是,在正常人类血清存在的情况下,这 4 种 mAbs 中的 3 种,2T5C9、2G9C 和 T1F11,保留了对来自 2 位家族性淀粉样多神经病(FAP)患者的 TTR 淀粉样纤维的低 nM 结合。两种最有前途的 mAbs,2T5C9 和 2G9C,也通过免疫组织化学显示对来自 2 位 FAP 患者的心脏组织切片中的 TTR 淀粉样沉积物具有低 nM 结合。综上所述,这些发现强烈支持进一步研究 TTR 聚集体特异性 mAbs 对 TTR 淀粉样变性患者的诊断效用。