Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Clinical Gastroenterology Unit, Careggi University Hospital, Florence, Italy.
Sci Rep. 2019 Feb 14;9(1):2064. doi: 10.1038/s41598-018-37950-4.
Therapeutic drug and immunogenicity monitoring (TDIM) is increasingly proposed to guide therapy with biologics, characterised by high inter-individual variability of their blood levels, to permit objective decisions for the management of non-responders and reduce unnecessary interventions with these expensive treatments. However, TDIM has not yet entered clinical practice partly because of uncertainties regarding the accuracy and precision of enzyme-linked immunosorbent assays (ELISA). Here we report the characterisation of a novel surface plasmon resonance (SPR)-based TDIM, applied to the measurement of serum concentrations of infliximab, an antibody against tumour necrosis factor α (anti-TNFα), and anti-infliximab antibodies. SPR has the obvious advantages of directly detecting and measuring serum antibodies in minutes, avoiding the long incubation/separation/washing/detection steps of the methods proposed so far, reducing complexity and variability. Moreover, drug and anti-drug antibodies can be measured simultaneously. This new method was validated for sensitivity and reproducibility, and showed cost-effectiveness over commercial ELISA kits. This method may be applied to other biotherapeutics. These data pave the way for the development of SPR-based point-of-care devices for rapid on-site analysis.
治疗药物和免疫原性监测(TDIM)越来越多地被提议用于指导生物制剂的治疗,这些药物的血药浓度个体间差异很大,因此可以客观地为无应答者的治疗做出决策,并减少对这些昂贵治疗方法的不必要干预。然而,TDIM 尚未进入临床实践,部分原因是酶联免疫吸附测定(ELISA)的准确性和精密度存在不确定性。在这里,我们报告了一种新型基于表面等离子体共振(SPR)的 TDIM 的特征,该方法应用于测量血清中肿瘤坏死因子 α(抗 TNFα)抗体英夫利昔单抗的浓度和抗英夫利昔单抗抗体。SPR 具有明显的优势,它可以在几分钟内直接检测和测量血清抗体,避免了迄今为止提出的方法的漫长孵育/分离/洗涤/检测步骤,从而降低了复杂性和变异性。此外,还可以同时测量药物和抗体。该新方法已针对灵敏度和重现性进行了验证,并显示出比商业 ELISA 试剂盒更具成本效益。该方法可应用于其他生物疗法。这些数据为基于 SPR 的即时检测设备的快速现场分析的开发铺平了道路。