Department of Public Health and Caring Sciences/Molecular Geriatrics, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
J Alzheimers Dis. 2010;21(4):1295-301. doi: 10.3233/jad-2010-100609.
Amyloid-β (Aβ) oligomers of different sizes and forms have recently been the focus formany Alzheimer's disease (AD) researchers. Various immunoassays have been used to detect low concentrations of these elusive Aβ species in different forms of human samples using little or no sample dilutions. However, the possibility that positive results may be caused by interference from heterophilic antibodies (HA) is often overlooked. HA, which recognize immunoglobulins from other species, are present in human plasma and cerebrospinal fluid (CSF) and may cause interference in sandwich immunoassays like enzyme-linked immunosorbent assays (ELISAs) by cross-binding the capture and detection antibodies of the assay. They thus may generate a false positive signal. Here we show that when assessing the Aβ oligomer content in plasma samples from 44 individuals with a sandwich ELISA, none of the 21 positive signals remained when the assay was repeated in the presence of factors blocking HA. Similarly, in CSF samples from 104 individuals, the signals from the 22 positive samples were strongly reduced when analyzed after anti-HA treatment. Taken together, HA interference is a problem that needs to be addressed when measuring low levels of an antigen in human plasma and CSF samples.
不同大小和形式的淀粉样蛋白-β (Aβ) 寡聚体最近成为许多阿尔茨海默病 (AD) 研究人员关注的焦点。已经使用了各种免疫测定法,通过很少或不稀释样本,来检测不同形式的人类样本中这些难以捉摸的 Aβ 物种的低浓度。然而,阳性结果可能是由异嗜性抗体 (HA) 干扰引起的可能性常常被忽视。HA 识别来自其他物种的免疫球蛋白,存在于人类血浆和脑脊液 (CSF) 中,并可能通过交叉结合测定的捕获和检测抗体,在夹心免疫测定(如酶联免疫吸附测定 (ELISA))中引起干扰。因此,它们可能会产生假阳性信号。在这里,我们展示了当使用夹心 ELISA 评估来自 44 名个体的血浆样本中的 Aβ 寡聚物含量时,当在存在阻断 HA 的因素的情况下重复测定时,21 个阳性信号中没有一个仍然存在。同样,在来自 104 名个体的 CSF 样本中,在经过抗 HA 处理后分析时,22 个阳性样本的信号被强烈降低。总之,HA 干扰是在测量人类血浆和 CSF 样本中低水平抗原时需要解决的问题。