School of Dentistry, Division of Foundational Sciences, University of Alberta, Edmonton, Alberta, Canada.
Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.
mBio. 2021 May 4;12(3):e00384-21. doi: 10.1128/mBio.00384-21.
The outbreak of SARS-CoV-2 infection has enormously impacted our lives. Clinical evidence has implicated the emergence of cytokine release syndrome as the prominent cause of mortality in COVID-19 patients. In this study, we observed massive elevation of plasma Galectin-9 (Gal-9) in COVID-19 patients compared to healthy controls (HCs). By using the receiver operating characteristic (ROC) curve, we found that a baseline of 2,042 pg/ml plasma Gal-9 can differentiate SARS-CoV-2-infected from noninfected individuals with high specificity/sensitivity (95%). Analysis of 30 cytokines and chemokines detected a positive correlation of the plasma Gal-9 with C-reactive protein (CRP) and proinflammatory cytokines/chemokines such as interleukin-6 (IL-6), tumor necrosis factor alpha (TNF-α), IP-10, MIP-1α, and MCP-1 but an inverse correlation with transforming growth factor β (TGF-β) in COVID-19 patients. In agreement, we found enhanced production of IL-6 and TNF-α by monocytes and NK cells of COVID-19 patients once treated with the recombinant human Gal-9 Also, we observed that although the cell-membrane expression of Gal-9 on monocytes does not change in COVID-19 patients, those with higher Gal-9 expression exhibit an activated phenotype. Furthermore, we noted significant downregulation of surface Gal-9 in neutrophils from COVID-19 patients compared to HCs. Our further investigations indicated that immune activation following SARS-CoV-2 infection results in Gal-9 shedding from neutrophils. The strong correlation of Gal-9 with proinflammatory mediators suggests that inhibition of Gal-9 may severe as a therapeutic approach in COVID-19 infection. Besides, the plasma Gal-9 measurement may be used as a surrogate diagnostic biomarker in COVID-19 patients. The outbreak of SARS-CoV-2 infection has enormously impacted our lives. Clinical evidence has implicated the emergence of cytokine release syndrome as the prominent cause of mortality in COVID-19 patients. We observed substantial elevation of the plasma Galectin-9 (Gal-9) in COVID-19 patients compared to healthy controls. Gal-9 is an abundant protein in many immune and nonimmune cells. We found that Gal-9 detection assay can differentiate SARS-CoV-2-infected from noninfected individuals with a specificity/sensitivity of 95%. Importantly, we found a positive correlation of the plasma Gal-9 with a wide range of proinflammatory biomarkers in COVID-19 patients. In agreement, we found enhanced expression and production of such proinflammatory molecules by immune cells of COVID-19 patients once treated with Gal-9 Our results propose Gal-9 as an important contributing factor in cytokine release syndrome; therefore, Gal-9 inhibition may serve as a beneficial therapeutic approach by suppressing the hyperimmune activation in COVID-19 patients.
SARS-CoV-2 感染的爆发极大地影响了我们的生活。临床证据表明,细胞因子释放综合征的出现是 COVID-19 患者死亡的主要原因。在这项研究中,我们观察到 COVID-19 患者血浆 Galectin-9(Gal-9)水平显著升高,与健康对照组(HCs)相比。通过使用受试者工作特征(ROC)曲线,我们发现基线 2042pg/ml 血浆 Gal-9 可以区分 SARS-CoV-2 感染与非感染个体,具有高特异性/敏感性(95%)。对 30 种细胞因子和趋化因子的分析表明,血浆 Gal-9 与 C 反应蛋白(CRP)和促炎细胞因子/趋化因子呈正相关,如白细胞介素 6(IL-6)、肿瘤坏死因子-α(TNF-α)、IP-10、MIP-1α 和 MCP-1,但与 COVID-19 患者的转化生长因子-β(TGF-β)呈负相关。同样,我们发现 COVID-19 患者的单核细胞和 NK 细胞一旦用重组人 Gal-9 处理,IL-6 和 TNF-α的产生增加。此外,我们发现,尽管 COVID-19 患者单核细胞表面 Gal-9 的表达没有变化,但表达更高 Gal-9 的细胞表现出激活表型。此外,我们注意到 COVID-19 患者中性粒细胞表面 Gal-9 的表达显著下调与 HCs 相比。我们的进一步研究表明,SARS-CoV-2 感染后的免疫激活导致中性粒细胞释放 Gal-9。Gal-9 与促炎介质的强相关性表明,抑制 Gal-9 可能是 COVID-19 感染的一种治疗方法。此外,血浆 Gal-9 测量可作为 COVID-19 患者的替代诊断生物标志物。SARS-CoV-2 感染的爆发极大地影响了我们的生活。临床证据表明,细胞因子释放综合征的出现是 COVID-19 患者死亡的主要原因。与健康对照组(HCs)相比,我们观察到 COVID-19 患者血浆 Galectin-9(Gal-9)水平显著升高。Gal-9 是许多免疫和非免疫细胞中丰富的蛋白质。我们发现 Gal-9 检测可以区分 SARS-CoV-2 感染与非感染个体,特异性/敏感性为 95%。重要的是,我们发现 COVID-19 患者血浆 Gal-9 与广泛的促炎生物标志物呈正相关。同样,我们发现 Gal-9 处理后 COVID-19 患者的免疫细胞表达和产生了这种促炎分子。我们的研究结果表明 Gal-9 是细胞因子释放综合征的一个重要因素;因此,Gal-9 抑制可能通过抑制 COVID-19 患者的过度免疫激活作为一种有益的治疗方法。