Study of the immune response in nested cases in a cohort to evaluate the effect of antiretrovirals on the evolution of the SARS-COV-2 coronavirus infection.

  • Funded by National Institute of Health Carlos III [El Instituto de Salud Carlos III] (ISCIII)
  • Total publications:0 publications

Grant number: COV20_00207

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Key facts

  • Disease

    COVID-19
  • Funder

    National Institute of Health Carlos III [El Instituto de Salud Carlos III] (ISCIII)
  • Principal Investigator

    Carolina Cubillos Zapata
  • Research Location

    Spain
  • Lead Research Institution

    Fundación para la Investigación Biomédica del Hospital Universitario La Paz
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Immunity

  • Special Interest Tags

    N/A

  • Study Type

    Clinical

  • Clinical Trial Details

    Unspecified

  • Broad Policy Alignment

    Pending

  • Age Group

    Unspecified

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

Patients infected with the CoVid-19 virus are characterized by a high degree of inflammation and dysregulation of the specific T response. In studies carried out with patients from the Hospital Universitario La Paz with respiratory diseases, we have found that the hypoxia and oxidative stress suffered by these patients cause the inflammasome complex to be activated. This complex also has effects on pyroptosis and on the production of type I IFNs. On the other hand, the inflammatory condition of the patient will directly condition the specific T response. In short, understanding the inflammatory state in patients provides relevant information on the evolution of the pathology. The aim of this project is to study the effect of the drugs included in this clinical trial in patients with CoVid-19, on the activation of the inflammasome and its effect on inflammation and the T response. These data associated with the evolution of the patient are determinants to classify responding patients and mechanisms of viral evasion.