Prospective evaluation of the production of lipid mediators in the immune response against COVID-19: search for biomarkers and new therapeutic targets in the evolution of the disease

  • Funded by Fundação de Amparo à Pesquisa do Estado de São Paulo [São Paulo Research Foundation] (FAPESP)
  • Total publications:0 publications

Grant number: 20/05207-6

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2022
  • Funder

    Fundação de Amparo à Pesquisa do Estado de São Paulo [São Paulo Research Foundation] (FAPESP)
  • Principal Investigator

    Lúcia Helena Faccioli
  • Research Location

    Brazil
  • Lead Research Institution

    Universidade de São Paulo
  • Research Priority Alignment

    N/A
  • Research Category

    Clinical characterisation and management

  • Research Subcategory

    Prognostic factors for disease severity

  • Special Interest Tags

    N/A

  • Study Type

    Clinical

  • Clinical Trial Details

    Not applicable

  • Broad Policy Alignment

    Pending

  • Age Group

    Unspecified

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

Due to the great spread of the new SARS-COV-2 coronavirus, we are experiencing a pandemic. COVID-19 disease, caused by this coronavirus, can have moderate to severe complications, especially in male, elderly and / or patients with underlying diseases. Severe cases present the "cytokine storm", with an exacerbated inflammatory response in the lung, the organ most affected. This project therefore seeks to identify molecular factors of susceptibility and resistance, as well as biomarkers of susceptibility and clinical evolution in COVID-19. To this end, we will investigate the inflammatory profile of patients by detecting and quantifying lipid mediators, including eicosanoids, steroid hormones and compounds derived from sphingolipids and ceramides, to look for a possible association with the clinical outcomes of COVID-19 and with components of the immune response, such as cytokines, chemokines and N-glycans profiles of IgG Ecs. In a case-control study approach, control participants (non-infected and asymptomatic) and patients treated at Hospital São Paulo in the city of Ribeirão Preto will be recruited, who will be evaluated clinically and laboratory by the doctors responsible for the care; proof of infection with SARS-COV-2 will be made in all participants. Plasma and leukocytes (buffy coat) will be obtained from the blood of participants. Protein inflammatory mediators will be quantified in plasma, as well as eicosanoids, steroid hormones, compounds derived from sphingolipids and ceramides. For this, through the use of mass spectrometry, we propose a multidisciplinary approach to identify lipid biomarkers related to the inflammatory process in COVID-19. The profiles of N-glycans in the Fcs of IgGs will be evaluated, according to the team's previous experience. The cells obtained will be frozen in Trizol, for further RNA extraction and analysis of gene expression. With these results, it is expected to understand in more detail, the pathophysiology of COVID-19, to establish markers of disease evolution and morbidity, as well as new targets for therapeutic interventions in patients infected with SARS-COV-2. (AU) The cells obtained will be frozen in Trizol, for further RNA extraction and analysis of gene expression. With these results, it is expected to understand in more detail, the pathophysiology of COVID-19, to establish markers of disease evolution and morbidity, as well as new targets for therapeutic interventions in patients infected with SARS-COV-2. (AU) The cells obtained will be frozen in Trizol, for further RNA extraction and analysis of gene expression. With these results, it is expected to understand in more detail, the pathophysiology of COVID-19, to establish markers of disease evolution and morbidity, as well as new targets for therapeutic interventions in patients infected with SARS-COV-2. (AU)