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开发一种通过DELFIA免疫测定法检测干血斑上SARS-CoV-2核衣壳抗体的方法。

Development of a Method for Detection of SARS-CoV-2 Nucleocapsid Antibodies on Dried Blood Spot by DELFIA Immunoassay.

作者信息

Damiani Verena, Pizzinato Erika, Cicalini Ilaria, Demattia Gianmaria, Zucchelli Mirco, Natale Luca, Palmarini Claudia, Di Marzio Claudia, Federici Luca, De Laurenzi Vincenzo, Pieragostino Damiana

机构信息

Center for Advanced Studies and Technology (CAST), "G. d'Annunzio" University of Chieti-Pescara, 66100 Chieti, Italy.

Department of Innovative Technologies in Medicine and Dentistry, "G. d'Annunzio" University of Chieti-Pescara, 66100 Chieti, Italy.

出版信息

Diagnostics (Basel). 2023 Feb 27;13(5):897. doi: 10.3390/diagnostics13050897.

Abstract

Antibodies against the SARS-CoV-2 nucleocapsid protein are produced by the immune system in response to SARS-CoV-2 infection, but most available vaccines developed to fight the pandemic spread target the SARS-CoV-2 spike protein. The aim of this study was to improve the detection of antibodies against the SARS-CoV-2 nucleocapsid by providing a simple and robust method applicable to a large population. For this purpose, we developed a DELFIA immunoassay on dried blood spots (DBSs) by converting a commercially available IVD ELISA assay. A total of forty-seven paired plasma and dried blood spots were collected from vaccinated and/or previously SARS-CoV-2-infected subjects. The DBS-DELFIA resulted in a wider dynamic range and higher sensitivity for detecting antibodies against the SARS-CoV-2 nucleocapsid. Moreover, the DBS-DELFIA showed a good total intra-assay coefficient of variability of 14.6%. Finally, a strong correlation was found between SARS-CoV-2 nucleocapsid antibodies detected by the DBS-DELFIA and ELISA immunoassays ( = 0.9). Therefore, the association of dried blood sampling with DELFIA technology may provide an easier, minimally invasive, and accurate measurement of SARS-CoV-2 nucleocapsid antibodies in previously SARS-CoV-2-infected subjects. In conclusion, these results justify further research to develop a certified IVD DBS-DELFIA assay for detecting SARS-CoV-2 nucleocapsid antibodies useful for diagnostics as well as for serosurveillance studies.

摘要

针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)核衣壳蛋白的抗体是免疫系统在SARS-CoV-2感染后产生的,但大多数为抗击这一疫情大流行而研发的现有疫苗都以SARS-CoV-2刺突蛋白为靶点。本研究的目的是通过提供一种适用于大量人群的简单且可靠的方法,来改进对SARS-CoV-2核衣壳抗体的检测。为此,我们通过对一种市售的体外诊断酶联免疫吸附测定(ELISA)法进行改造,开发了一种基于干血斑(DBS)的时间分辨荧光免疫分析(DELFIA)法。我们从接种过疫苗和/或先前感染过SARS-CoV-2的受试者中总共收集了47对血浆和干血斑样本。基于干血斑的时间分辨荧光免疫分析在检测针对SARS-CoV-2核衣壳的抗体方面具有更宽的动态范围和更高的灵敏度。此外,基于干血斑的时间分辨荧光免疫分析显示出良好的总批内变异系数,为14.6%。最后,发现基于干血斑的时间分辨荧光免疫分析和ELISA免疫分析检测到的SARS-CoV-2核衣壳抗体之间存在很强的相关性( = 0.9)。因此,干血采样与时间分辨荧光免疫分析技术相结合,可能为先前感染过SARS-CoV-2的受试者提供一种更简便、微创且准确的SARS-CoV-2核衣壳抗体检测方法。总之,这些结果证明有必要进一步开展研究,以开发一种经过认证的体外诊断基于干血斑的时间分辨荧光免疫分析方法,用于检测对诊断和血清学监测研究有用的SARS-CoV-2核衣壳抗体。

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