| Literature DB >> 34944005 |
Ivan Vlasov1, Alexandra Panteleeva2,3, Tatiana Usenko2,3, Mikhael Nikolaev2,3, Artem Izumchenko3, Elena Gavrilova2, Irina Shlyk2, Valentina Miroshnikova2,3, Maria Shadrina1, Yurii Polushin2, Sofya Pchelina2,3,4, Petr Slonimsky1.
Abstract
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.Entities:
Keywords: COVID-19; GO ontology; LDL particle receptor activity; cargo receptor activity; leukocyte differentiation; peripheral blood mononuclear cells; transcriptome
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Year: 2021 PMID: 34944005 PMCID: PMC8700658 DOI: 10.3390/cells10123495
Source DB: PubMed Journal: Cells ISSN: 2073-4409 Impact factor: 6.600