Department of Biotechnology, Centre of Systems Biology, Biomedical Research Foundation of the Academy of Athens, 11527 Athens, Greece.
Department of Clinical Pharmacology, School of Medicine, Aristotle University of Thessaloniki, 54636 Thessaloniki, Greece.
Int J Mol Sci. 2022 Sep 5;23(17):10153. doi: 10.3390/ijms231710153.
Over the course of the pandemic, proteomics, being in the frontline of anti-COVID-19 research, has massively contributed to the investigation of molecular pathogenic properties of the virus. However, data on the proteome on anti-SARS-CoV-2 vaccinated individuals remain scarce. This study aimed to identify the serum proteome characteristics of anti-SARS-CoV-2 vaccinated individuals who had previously contracted the virus and comparatively assess them against those of virus-naïve vaccine recipients. Blood samples of = 252 individuals, out of whom = 35 had been previously infected, were collected in the "G. Gennimatas" General Hospital of Thessaloniki, from 4 January 2021 to 31 August 2021. All participants received the BNT162b2 mRNA COVID-19 vaccine (Pfizer/BioNTech). A label-free quantitative proteomics LC-MS/MS approach was undertaken, and the identified proteins were analyzed using the GO (Gene Ontology) and KEGG (Kyoto Encyclopedia of Genes) databases as well as processed by bioinformatics tools. Titers of total RBD-specific IgGs against SARS-CoV-2 were also determined using the SARS-CoV-2 IgG II Quant assay. A total of 47 proteins were significantly differentially expressed, the majority of which were down-regulated in sera of previously infected patients compared to virus-naïve controls. Several pathways were affected supporting the crucial role of the humoral immune response in the protection against SARS-CoV-2 infection provided by COVID-19 vaccination. Overall, our comprehensive proteome profiling analysis contributes novel knowledge of the mechanisms of immune response induced by anti-SARS-CoV-2 vaccination and identified protein signatures reflecting the immune status of vaccine recipients.
在大流行期间,蛋白质组学作为抗 COVID-19 研究的前沿领域,为研究病毒的分子发病特性做出了巨大贡献。然而,关于接种 SARS-CoV-2 疫苗的个体的蛋白质组数据仍然很少。本研究旨在鉴定先前感染过该病毒的接种 SARS-CoV-2 疫苗的个体的血清蛋白质组特征,并将其与未感染病毒的疫苗接种者进行比较评估。2021 年 1 月 4 日至 2021 年 8 月 31 日,在塞萨洛尼基的“G. Gennimatas”综合医院采集了 252 名个体的血液样本,其中 35 名个体曾被感染。所有参与者均接种了 BNT162b2 mRNA COVID-19 疫苗(辉瑞/生物技术)。采用无标记定量蛋白质组学 LC-MS/MS 方法,使用 GO(基因本体论)和 KEGG(京都基因与基因组百科全书)数据库对鉴定的蛋白质进行分析,并通过生物信息学工具进行处理。使用 SARS-CoV-2 IgG II Quant 测定法还测定了针对 SARS-CoV-2 的总 RBD 特异性 IgG 的滴度。共有 47 种蛋白质的表达水平存在显著差异,与未感染病毒的对照组相比,大多数先前感染患者的血清中这些蛋白质表达下调。多个途径受到影响,支持体液免疫反应在 COVID-19 疫苗接种提供的 SARS-CoV-2 感染保护中的关键作用。总的来说,我们全面的蛋白质组谱分析为 SARS-CoV-2 疫苗接种诱导的免疫反应机制提供了新的知识,并确定了反映疫苗接种者免疫状态的蛋白质特征。