Bonnez Quintijn, Dekimpe Charlotte, Tellier Edwige, Kaplanski Gilles, Verhamme Peter, Tersteeg Claudia, De Meyer Simon F, Lammertyn Jeroen, Joly Bérangère, Coppo Paul, Veyradier Agnès, Vanhoorelbeke Karen
Laboratory for Thrombosis Research, IRF Life Sciences, KU Leuven Campus Kulak Kortrijk, Kortrijk, Belgium.
Aix-Marseille University, Institut National de la Santé et de la Recherche Médicale, INRAE, C2VN, Marseille, France.
Res Pract Thromb Haemost. 2023 Aug 19;7(6):102171. doi: 10.1016/j.rpth.2023.102171. eCollection 2023 Aug.
Thrombotic thrombocytopenic purpura (TTP) is characterized by severe ADAMTS-13 activity deficiency (<10%). Diagnostic testing is challenging because of unavailability, high cost, and expert technician requirement of ADAMTS-13 enzyme assays. Cost-effective, automated fiber-optic surface plasmon resonance (FO-SPR) platforms show potential for developing diagnostic tests. Yet, FO-SPR has never been explored to measure enzymatic activities.
To develop an easy-to-use ADAMTS-13 activity assay utilizing optical fibers to rapidly diagnose TTP.
The ADAMTS-13 activity assay was designed and optimized using FO-SPR technology based on a previously described enzyme-linked immunosorbent assay setup. A calibration curve was generated to quantify ADAMTS-13 activity in plasma of healthy donors and patients with acute immune-mediated TTP (iTTP), hemolytic uremic syndrome, or sepsis. ADAMTS-13 activity data from FO-SPR and fluorescence resonance energy transfer-based strategies (FRETS)-VWF73 reference assays were compared.
After initial assay development, optimization improved read-out magnitude and signal-to-noise ratio and reduced variation. Further characterization demonstrated a detection limit (6.8%) and inter-assay variation (Coefficient of variation, 7.2%) that showed good analytical sensitivity and repeatability. From diverse plasma samples, only plasma from patients with acute iTTP showed ADAMTS-13 activities below 10%. Strong Pearson correlation ( = 0.854) between FO-SPR and reference FRETS-VWF73 assays were observed for all measured samples.
A fast ADAMTS-13 activity assay was designed onto automated FO-SPR technology. Optimization resulted in sensitive ADAMTS-13 activity measurements with a detection limit enabling clinical diagnosis of TTP within 3 hours. The FO-SPR assay proved strong correlation with the reference FRETS-VWF73 assay. For the first time, this assay demonstrated the capacity of FO-SPR technology to measure enzymatic activity in pre-clinical context.
血栓性血小板减少性紫癜(TTP)的特征是严重的ADAMTS-13活性缺乏(<10%)。由于ADAMTS-13酶检测方法难以获得、成本高昂且需要专业技术人员,诊断测试具有挑战性。具有成本效益的自动化光纤表面等离子体共振(FO-SPR)平台显示出开发诊断测试的潜力。然而,从未探索过使用FO-SPR来测量酶活性。
开发一种利用光纤的易于使用的ADAMTS-13活性检测方法,以快速诊断TTP。
基于先前描述的酶联免疫吸附测定设置,使用FO-SPR技术设计并优化ADAMTS-13活性检测方法。生成校准曲线以量化健康供体以及急性免疫介导的TTP(iTTP)、溶血尿毒综合征或脓毒症患者血浆中的ADAMTS-13活性。比较了FO-SPR和基于荧光共振能量转移策略(FRETS)-VWF73参考检测方法的ADAMTS-13活性数据。
在初步开发检测方法后,优化提高了读出幅度和信噪比并减少了变异。进一步的特性表征显示出检测限(6.8%)和批间变异(变异系数,7.2%),表明具有良好的分析灵敏度和重复性。在各种血浆样本中,只有急性iTTP患者的血浆显示ADAMTS-13活性低于10%。对于所有测量样本,观察到FO-SPR与参考FRETS-VWF73检测方法之间具有很强的Pearson相关性(r = 0.854)。
在自动化FO-SPR技术上设计了一种快速的ADAMTS-13活性检测方法。优化后实现了对ADAMTS-13活性的灵敏测量,其检测限能够在3小时内对TTP进行临床诊断。FO-SPR检测方法与参考FRETS-VWF73检测方法具有很强的相关性。该检测方法首次证明了FO-SPR技术在临床前环境中测量酶活性的能力。