Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, St. Louis, MO, United States.
Thrombosis Research Laboratory, Department of Cardiac-Thoracic-Vascular Sciences and Public Health, University of Padova, Padua, Italy.
Front Immunol. 2021 Sep 8;12:741589. doi: 10.3389/fimmu.2021.741589. eCollection 2021.
Autoantibodies targeting prothrombin (aPT) can be found in antiphospholipid syndrome (APS) patients. However, their detection has proven difficult to standardize. Here, we developed a new ELISA assay to improve the identification of aPT and compared its performance with currently available anti-phosphatidylserine/prothrombin antibodies (aPS/PT) and autoantibodies targeting prothrombin bound to the plastic plate (aPT-A) assays using a cohort of 27 APS patients at high risk of thrombosis. We generated a novel prothrombin variant, ProTS525A-Biot, carrying an artificial tag at the C-terminus suitable for site-specific biotinylation and added the mutation S525A to improve stability. ProTS525A-Biot was immobilized to neutravidin-coated plates at the desired density and with a defined orientation, i.e., pointing the N-terminal fragment-1 toward the solvent. Antibodies against ProTS525A-Biot (aPT-Bio) were found in 24 out of 27 triple-positive APS patients (88%). When compared to aPS/PT and aPT-A, aPT-Bio showed an excellent linear correlation with aPS/PT (R 0.85) but not with aPT-A (R 0.40). Since aPS/PT but not aPT-A are an emerging biomarker of thrombosis in APS, this method may find utility for detecting pathogenic aPT in APS but also other prothrombotic conditions such as COVID-19.
针对凝血酶原的自身抗体(aPT)可在抗磷脂综合征(APS)患者中发现。然而,其检测一直难以标准化。在这里,我们开发了一种新的 ELISA 检测方法来提高对 aPT 的识别能力,并使用高血栓风险的 APS 患者队列比较了其与当前可用的抗磷脂酰丝氨酸/凝血酶原抗体(aPS/PT)和针对与塑料板结合的凝血酶原的自身抗体(aPT-A)检测方法的性能。我们生成了一种新型凝血酶原变体 ProTS525A-Biot,在 C 末端带有适合位点特异性生物素化的人工标签,并添加了突变 S525A 以提高稳定性。ProTS525A-Biot 以所需的密度和定义的方向固定在链霉亲和素包被的平板上,即指向溶剂的 N 端片段-1。在 27 例三重阳性 APS 患者中发现了 24 例针对 ProTS525A-Biot 的抗体(88%)。与 aPS/PT 和 aPT-A 相比,aPT-Bio 与 aPS/PT 显示出极好的线性相关性(R 0.85),但与 aPT-A 无相关性(R 0.40)。由于 aPS/PT 而不是 aPT-A 是 APS 中血栓形成的新兴生物标志物,因此该方法可能有助于检测 APS 中的致病性 aPT,但也有助于检测其他促血栓形成情况,如 COVID-19。