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一种用于检测抗磷脂综合征高血栓风险患者抗凝血酶原抗体的新型 ELISA 检测方法。

A Novel ELISA Assay for the Detection of Anti-Prothrombin Antibodies in Antiphospholipid Syndrome Patients at High Risk of Thrombosis.

机构信息

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.

出版信息

Front Immunol. 2021 Sep 8;12:741589. doi: 10.3389/fimmu.2021.741589. eCollection 2021.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e9/8455811/2b8f939bd1d6/fimmu-12-741589-g001.jpg

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