Publications by authors named "I A Polkovnikova"

Article Synopsis
  • tRNA-derived fragments (tRFs) serve both as biomarkers and signaling molecules in various disorders, with their expression patterns differing among blood cell types and changing with physiological conditions, such as during COVID-19.
  • The research compared tRF expression in different blood cells (erythrocytes, monocytes, lymphocytes, etc.) from both healthy donors and severe COVID-19 patients using fluorescence sorting and next-generation sequencing.
  • The study found significant changes in tRF patterns in multiple cell types during severe COVID-19, indicating that distinct blood cells respond differently to cytokine storms, which may involve regulation through nucleotide modifications and RNA enzyme activity alterations.
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Non-coding RNA expression has shown to have cell type-specificity. The regulatory characteristics of these molecules are impacted by changes in their expression levels. We performed next-generation sequencing and examined small RNA-seq data obtained from 6 different types of blood cells separated by fluorescence-activated cell sorting of severe COVID-19 patients and healthy control donors.

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Coronavirus disease (COVID-19) has become a global pandemic. COVID-19 patients need immediate diagnosis and rehabilitation, which makes it urgent to identify new protein markers for a prognosis of the severity and outcome of the disease. The aim of this study was to analyze the levels of interleukin-6 (IL-6) and secretory phospholipase (sPLA2) in the blood of patients regarding the severity and outcome of COVID-19 infection.

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We studied the differences in the characteristics of T-cell immunity in clinically healthy volunteers of three groups: "no previous COVID-19, not vaccinated", "recovered", and "vaccinated" as well as the relationship between the presence of IFNγ-releasing T cells in response to stimulation with peptide pools overlapping the main S, N, M, ORF3, and ORF7 protein sequences and the presence of IgG to the SARS-CoV-2 S protein. In the "no previous COVID-19, non-vaccinated" group, T cells specific to both S protein and other virus proteins were absent in 95% subjects. In the "recovered from COVID-19" group, T cells specific to the spike protein were present in samples from 39% subjects.

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