The immunologic and virologic determinants of long COVID

  • Funded by Department of Health and Social Care / National Institute for Health and Care Research (DHSC-NIHR)
  • Total publications:9 publications

Grant number: COV-LT2-0041

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2021
    2024
  • Known Financial Commitments (USD)

    $1,079,790.66
  • Funder

    Department of Health and Social Care / National Institute for Health and Care Research (DHSC-NIHR)
  • Principal Investigator

    N/A

  • Research Location

    United Kingdom
  • Lead Research Institution

    Cardiff University
  • Research Priority Alignment

    N/A
  • Research Category

    Clinical characterisation and management

  • Research Subcategory

    Disease pathogenesis

  • 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

Coronavirus infection has been confirmed in over 157 million people worldwide and over 4 million people in the UK. Initially, there was understandable focus on the care of patients hospitalized with severe disease, but it has subsequently been recognized that many individuals managed their symptoms in the community during the acute phase of COVID-19. The long-term effects of infection in both groups are now becoming apparent. Long COVID describes a broad range of symptoms that persist 12 weeks after acute infection with SARS-CoV-2. Symptoms are diverse and commonly include fatigue, breathlessness, cognitive impairment ("brain fog"), chest pain, palpitations, and persistent disturbances in smell and taste. Data from the Office for National Statistics suggest that over a million people in the suffer with long COVID in the UK. The potential economic impact and anticipated burden faced by the NHS as a consequence of long COVID has been acknowledged more recently, and a spotlight has been focused on the need for research into the multisystem effects of the condition to inform the future development of diagnostics and therapeutic strategies. Published studies have emphasized the importance of immune responses during acute COVID19. However, little is known about the role of the immune system in long COVID. Our study aims to investigate the hypothesis that overactive or maladaptive immune responses drive ongoing systemic inflammation and clinical symptoms in patients with long COVID.

Publicationslinked via Europe PMC

Last Updated:41 minutes ago

View all publications at Europe PMC

Identification of soluble biomarkers that associate with distinct manifestations of long COVID.

Age differentially impacts adaptive immune responses induced by adenoviral versus mRNA vaccines against COVID-19.

SARS-CoV-2 vaccination enhances the effector qualities of spike-specific T cells induced by COVID-19.

Complement dysregulation is a prevalent and therapeutically amenable feature of long COVID.

Author Correction: Human circulating and tissue-resident memory CD8+ T cells.

Nucleocapsid-specific T cell responses associate with control of SARS-CoV-2 in the upper airways before seroconversion.

Human circulating and tissue-resident memory CD8+ T cells.

Ageing Curtails the Diversity and Functionality of Nascent CD8+ T Cell Responses against SARS-CoV-2.

Ancestral SARS-CoV-2-specific T cells cross-recognize the Omicron variant.