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用于检测自身免疫性疾病中自身抗体的光纤表面等离子体共振生物传感器上钴(III)-氮三乙酸介导的抗原固定化:在免疫介导的血栓性血小板减少性紫癜中的应用

Co(III)-NTA Mediated Antigen Immobilization on a Fiber Optic-SPR Biosensor for Detection of Autoantibodies in Autoimmune Diseases: Application in Immune-Mediated Thrombotic Thrombocytopenic Purpura.

作者信息

Horta Sara, Qu Jia-Huan, Dekimpe Charlotte, Bonnez Quintijn, Vandenbulcke Aline, Tellier Edwige, Kaplanski Gilles, Delport Filip, Geukens Nick, Lammertyn Jeroen, Vanhoorelbeke Karen

机构信息

Laboratory for Thrombosis Research, IRF Life Sciences, KU Leuven Campus Kulak Kortrijk, Etienne Sabbelaan 53, Kortrijk 8500, Belgium.

Department of Biosystems, Biosensors Group, KU Leuven, Willem De Croylaan 42, Heverlee B-3001, Belgium.

出版信息

Anal Chem. 2020 Oct 20;92(20):13880-13887. doi: 10.1021/acs.analchem.0c02586. Epub 2020 Sep 29.

Abstract

Autoantibodies are key biomarkers in clinical diagnosis of autoimmune diseases routinely detected by enzyme-linked immunosorbent assays (ELISAs). However, the complexity of these assays is limiting their use in routine diagnostics. Fiber optic-surface plasmon resonance (FO-SPR) can overcome these limitations, but improved surface chemistries are still needed to guarantee detection of autoantibodies in complex matrices. In this paper, we describe the development of an FO-SPR immunoassay for the detection of autoantibodies in plasma samples from immune-mediated thrombotic thrombocytopenic purpura (iTTP) patients. Hereto, hexahistidine-tagged recombinant ADAMTS13 (rADAMTS13-His) was immobilized on nitrilotriacetic acid (NTA)-coated FO probes chelated by cobalt (Co(III)) and exposed to anti-ADAMTS13 autoantibodies. Initial studies were performed to optimize rADAMTS13-His immobilization and to confirm the specificity of the immunoassay for detection of anti-ADAMTS13 autoantibodies with FO-SPR. The performance of the immunoassay was then evaluated by comparing Co(III)- and nickel (Ni(II))-NTA stabilized surfaces, confirming the stable immobilization of the antigen in Co(III)-NTA-functionalized FO probes. A calibration curve was prepared with a dilution series of a cloned human anti-ADAMTS13 autoantibody in ADAMTS13-depleted plasma resulting in an average interassay coefficient of variation of 7.1% and a limit of detection of 0.24 ng/mL. Finally, the FO-SPR immunoassay was validated using seven iTTP patient plasma samples, resulting in an excellent correlation with an in-house-developed ELISA ( = 0.973). In summary, the specificity and high sensitivity in combination with a short time-to-result (2.5 h compared to 4-5 h for a regular ELISA) make the FO-SPR immunoassay a powerful assay for routine diagnosis of iTTP and with extension for any other autoimmune disease.

摘要

自身抗体是自身免疫性疾病临床诊断中的关键生物标志物,通常通过酶联免疫吸附测定(ELISA)进行检测。然而,这些检测方法的复杂性限制了它们在常规诊断中的应用。光纤表面等离子体共振(FO-SPR)可以克服这些限制,但仍需要改进表面化学以确保在复杂基质中检测自身抗体。在本文中,我们描述了一种用于检测免疫介导的血栓性血小板减少性紫癜(iTTP)患者血浆样本中自身抗体的FO-SPR免疫测定方法的开发。为此,将六聚组氨酸标记的重组ADAMTS13(rADAMTS13-His)固定在由钴(Co(III))螯合的氮三乙酸(NTA)包被的FO探针上,并使其暴露于抗ADAMTS13自身抗体。进行了初步研究以优化rADAMTS13-His的固定,并通过FO-SPR确认免疫测定检测抗ADAMTS13自身抗体的特异性。然后通过比较Co(III)和镍(Ni(II))-NTA稳定的表面来评估免疫测定的性能,证实了抗原在Co(III)-NTA功能化的FO探针中的稳定固定。用ADAMTS13耗尽的血浆中克隆的人抗ADAMTS13自身抗体的稀释系列制备校准曲线,得到的平均批间变异系数为7.1%,检测限为0.24 ng/mL。最后,使用七个iTTP患者血浆样本对FO-SPR免疫测定进行了验证,结果与内部开发的ELISA具有极好的相关性( = 0.973)。总之,特异性和高灵敏度以及较短的出结果时间(2.5小时,而常规ELISA为4-5小时)使FO-SPR免疫测定成为iTTP常规诊断的有力检测方法,并可扩展用于任何其他自身免疫性疾病。

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