IL-6 and IL-18 cytokine traps in COVID-19

A. Korotaeva, E. Samoilova, D. A. Chepurnova, N. V. Pogosova, D. T. Kuchiev, F. N. Paleev
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Abstract

Cytokines are mediators of immunity that regulate inflammation. Intensity of inflammatory process is strongly dependent on the cytokine type and duration of its effect. Interleukin 6 (IL-6) and interleukin 18 (IL-18) play an important role in the initiation and progression of inflammation. Cytokines regulate the inflammatory process in different ways by inducing or inhibiting inflammatory reactions. Functional activity of cytokines is limited by trap molecules whose levels determine initiation of protective or pathological effects of interleukins. Soluble glycoprotein sgp130 functions as a trap for IL-6, while IL-18 is controlled by IL-18 binding protein (IL-18BP). High IL-6 and IL-18 levels were recorded in COVID-19 patients, being associated with unfavorable outcome of the disease. Our objective was to compare sgp130 and IL-18BP levels in patients with different degrees of COVID-19. Retrospective study included 74 COVID-19 patients (40 men and 34 women) aged 63±14 years. The patients were assigned to groups according to severity of lung damage. Group 1 included patients without lung damage; group 2, patients with moderate pneumonia ( 50% lung damage); group 3, patients with severe pneumonia ( 50% lung damage). Plasma levels of cytokines and their trap molecules were determined by quantitative immunoenzyme assay. IL-6 and IL-18 plasma concentrations increased with COVID-19 severity. Ambiguous changes were recorded for their traps. Plasma levels of sgp130 were lower in patients with moderate pneumonia than in patients without lung damage. In patients with severe pneumonia sgp130 plasma concentrations were higher than those in patients with mild pneumonia, being similar to those in patients without lung damage. In contrast to sgp130, IL-18BP levels decreased with COVID-19 severity. Thus, an increase in IL-6 and IL-18 levels parallel to COVID-19 severity is accompanied by ambiguous changes in the levels of their trap molecules. The ratio between the levels of IL-6 and IL-18 and their traps reflects the degree of COVID-19 severity.
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COVID-19 中的 IL-6 和 IL-18 细胞因子陷阱
细胞因子是调节炎症的免疫介质。炎症过程的强度在很大程度上取决于细胞因子的类型及其作用的持续时间。白细胞介素 6(IL-6)和白细胞介素 18(IL-18)在炎症的发生和发展过程中发挥着重要作用。细胞因子通过诱导或抑制炎症反应,以不同方式调节炎症过程。细胞因子的功能活性受到捕获分子的限制,捕获分子的水平决定了白细胞介素的保护或病理效应的启动。可溶性糖蛋白 sgp130 对 IL-6 起着捕获作用,而 IL-18 则受 IL-18 结合蛋白(IL-18BP)的控制。COVID-19患者的IL-6和IL-18水平较高,这与疾病的不良预后有关。我们的目的是比较不同程度 COVID-19 患者的 sgp130 和 IL-18BP 水平。回顾性研究纳入了 74 例 COVID-19 患者(男性 40 例,女性 34 例),年龄为 63±14 岁。根据肺损伤的严重程度将患者分组。第一组为无肺损伤患者;第二组为中度肺炎患者(肺损伤程度为 50%);第三组为重度肺炎患者(肺损伤程度为 50%)。血浆中细胞因子及其捕获分子的水平是通过定量免疫酶法测定的。IL-6和IL-18的血浆浓度随COVID-19的严重程度而增加。其捕获物的变化不明显。中度肺炎患者血浆中的 sgp130 水平低于无肺部损伤的患者。重症肺炎患者的 sgp130 血浆浓度高于轻症肺炎患者,但与无肺损伤患者的血浆浓度相似。与 sgp130 相反,IL-18BP 水平随着 COVID-19 的严重程度而降低。因此,IL-6 和 IL-18 水平的增加与 COVID-19 的严重程度平行,但其捕获分子水平的变化却不明确。IL-6和IL-18及其捕获分子水平之间的比率反映了COVID-19的严重程度。
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