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基于酶联免疫吸附测定的分析揭示了与疾病严重程度相关的抗SARS-CoV-2蛋白免疫反应谱。

ELISA-Based Analysis Reveals an Anti-SARS-CoV-2 Protein Immune Response Profile Associated with Disease Severity.

作者信息

Herrscher Charline, Eymieux Sébastien, Gaborit Christophe, Blasco Hélène, Marlet Julien, Stefic Karl, Roingeard Philippe, Grammatico-Guillon Leslie, Hourioux Christophe

机构信息

Inserm U1259 Morphogénèse et Antigénicité du VIH et des virus des Hépatites, Université de Tours et CHRU de Tours, 37000 Tours, France.

Epidémiologie des Données Cliniques en Centre-Val de Loire (EpiDcliC), Centre Hospitalier Universitaire de Tours, 37000 Tours, France.

出版信息

J Clin Med. 2022 Jan 14;11(2):405. doi: 10.3390/jcm11020405.

Abstract

Since the start of the COVID-19 pandemic, many studies have investigated the humoral response to SARS-CoV-2 during infection. Studies with native viral proteins constitute a first-line approach to assessing the overall immune response, but small peptides are an accurate and valuable tool for the fine characterization of B-cell epitopes, despite the restriction of this approach to the determination of linear epitopes. In this study, we used ELISA and peptides covering a selection of structural and non-structural SARS-CoV-2 proteins to identify key epitopes eliciting a strong immune response that could serve as a biological signature of disease characteristics, such as severity, in particular. We used 213 plasma samples from a cohort of patients well-characterized clinically and biologically and followed for COVID-19 infection. We found that patients developing severe disease had higher titers of antibodies mapping to multiple specific epitopes than patients with mild to moderate disease. These data are potentially important as they could be used for immunological profiling to improve our knowledge of the quantitative and qualitative characteristics of the humoral response in relation to patient outcome.

摘要

自新冠疫情开始以来,许多研究调查了感染期间对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的体液免疫反应。使用天然病毒蛋白的研究是评估整体免疫反应的一线方法,但小肽是精细表征B细胞表位的准确且有价值的工具,尽管这种方法仅限于确定线性表位。在本研究中,我们使用酶联免疫吸附测定(ELISA)和覆盖一系列SARS-CoV-2结构和非结构蛋白的肽段,以鉴定引发强烈免疫反应的关键表位,这些表位尤其可作为疾病特征(如严重程度)的生物学标志。我们使用了来自一组临床和生物学特征明确且随访了新冠病毒感染情况的患者的213份血浆样本。我们发现,与轻症至中症患者相比,发展为重症疾病的患者针对多个特定表位的抗体滴度更高。这些数据可能具有重要意义,因为它们可用于免疫分析,以增进我们对与患者预后相关的体液免疫反应的定量和定性特征的了解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf88/8781066/5ad53a10a71a/jcm-11-00405-g001.jpg

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