Institute of Molecular Genetics of National Research Center "Kurchatov Institute", 123182 Moscow, Russia.
Pavlov First Saint-Petersburg State Medical University, 197022 Saint-Petersburg, Russia.
Cells. 2021 Dec 10;10(12):3495. doi: 10.3390/cells10123495.
To assess the biology of the lethal endpoint in patients with SARS-CoV-2 infection, we compared the transcriptional response to the virus in patients who survived or died during severe COVID-19. We applied gene expression profiling to generate transcriptional signatures for peripheral blood mononuclear cells (PBMCs) from patients with SARS-CoV-2 infection at the time when they were placed in the Intensive Care Unit of the Pavlov First State Medical University of St. Petersburg (Russia). Three different bioinformatics approaches to RNA-seq analysis identified a downregulation of three common pathways in survivors compared with nonsurvivors among patients with severe COVID-19, namely, low-density lipoprotein (LDL) particle receptor activity (GO:0005041), important for maintaining cholesterol homeostasis, leukocyte differentiation (GO:0002521), and cargo receptor activity (GO:0038024). Specifically, PBMCs from surviving patients were characterized by reduced expression of PPARG, CD36, STAB1, ITGAV, and ANXA2. Taken together, our findings suggest that LDL particle receptor pathway activity in patients with COVID-19 infection is associated with poor disease prognosis.
为了评估 SARS-CoV-2 感染患者致死终点的生物学特性,我们比较了在重症 COVID-19 期间存活和死亡的患者对病毒的转录反应。我们应用基因表达谱分析生成了来自俄罗斯圣彼得堡巴甫洛夫第一国立医科大学重症监护病房(俄罗斯)感染 SARS-CoV-2 的患者外周血单核细胞(PBMC)的转录特征。三种不同的 RNA-seq 分析生物信息学方法确定了与非幸存者相比,重症 COVID-19 幸存者患者中三种常见途径的下调,即 LDL 颗粒受体活性(GO:0005041),对维持胆固醇稳态很重要,白细胞分化(GO:0002521)和货物受体活性(GO:0038024)。具体而言,来自存活患者的 PBMC 表现为 PPARG、CD36、STAB1、ITGAV 和 ANXA2 的表达降低。综上所述,我们的研究结果表明,COVID-19 感染患者的 LDL 颗粒受体途径活性与不良预后相关。