Sołkiewicz Katarzyna, Kokot Izabela, Kacperczyk Monika, Dymicka-Piekarska Violetta, Dorf Justyna, Kratz Ewa Maria
Department of Laboratory Diagnostics, Division of Laboratory Diagnostics, Faculty of Pharmacy, Wroclaw Medical University, Borowska Street 211a, 50-556 Wroclaw, Poland.
Department of Clinical Laboratory Diagnostics, Medical University of Bialystok, Waszyngtona 15A St., 15-269 Bialystok, Poland.
Int J Mol Sci. 2024 Apr 10;25(8):4198. doi: 10.3390/ijms25084198.
COVID-19 is an infectious disease caused by the SARS-CoV-2 virus. Glycoprotein clusterin (CLU) has many functions such as phagocyte recruitment, complement system inhibition, apoptosis inhibition, hormone and lipid transport, as well as in the immune response. The study aimed to assess the changes in CLU concentrations and the profile and degree of CLU glycosylation between patients with severe COVID-19, convalescents, and healthy subjects (control). The profile and degree of serum CLU N-glycosylation were analyzed using lectin-ELISA with specific lectins. CLU concentrations were significantly lower and relative reactivities of CLU glycans with SNA ( agglutinin) were significantly higher in severe COVID-19 patients in comparison to convalescents and the control group. The relative reactivities of CLU glycans with MAA ( agglutinin), together with relative reactivity with LCA ( agglutinin), were also significantly higher in patients with severe COVID-19 than in convalescents and the control group, but they also significantly differed between convalescents and control. The development of acute inflammation in the course of severe COVID-19 is associated with a decrease in CLU concentration, accompanied by an increase in the expression of α2,3-linked sialic acid, and core fucose. Both of these parameters can be included as useful glycomarkers differentiating patients with severe COVID-19 from convalescents and the control group, as well as convalescents and healthy subjects.
新型冠状病毒肺炎(COVID-19)是一种由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的传染病。糖蛋白簇集素(CLU)具有多种功能,如吞噬细胞募集、补体系统抑制、细胞凋亡抑制、激素和脂质转运以及免疫反应等。本研究旨在评估重症COVID-19患者、康复者和健康受试者(对照组)之间CLU浓度的变化以及CLU糖基化的特征和程度。使用特异性凝集素的凝集素酶联免疫吸附测定法(lectin-ELISA)分析血清CLU N-糖基化的特征和程度。与康复者和对照组相比,重症COVID-19患者的CLU浓度显著降低,且CLU聚糖与SNA(凝集素)的相对反应性显著升高。重症COVID-19患者的CLU聚糖与MAA(凝集素)的相对反应性以及与LCA(凝集素)的相对反应性也显著高于康复者和对照组,但康复者和对照组之间也存在显著差异。重症COVID-19病程中急性炎症的发展与CLU浓度降低有关,同时伴有α2,3连接唾液酸和核心岩藻糖表达增加。这两个参数均可作为区分重症COVID-19患者与康复者及对照组以及康复者与健康受试者的有用糖基化生物标志物。