Phase 1 COVID-19 Immunity - National Core Study

  • Funded by UK Research and Innovation (UKRI)
  • Total publications:87 publications

Grant number: MC_PC_20060

Grant search

Key facts

  • Disease

    COVID-19
  • Start & end year

    2021
    2022
  • Known Financial Commitments (USD)

    $10,563,730.11
  • Funder

    UK Research and Innovation (UKRI)
  • Principal Investigator

    Professor Paul Moss
  • Research Location

    United Kingdom
  • Lead Research Institution

    University of Birmingham
  • 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

    Not applicable

  • Broad Policy Alignment

    Pending

  • Age Group

    Adolescent (13 years to 17 years)Adults (18 and older)Older adults (65 and older)

  • Vulnerable Population

    Minority communities unspecifiedOther

  • Occupations of Interest

    Health PersonnelUnspecified

Abstract

The magnitude and quality of the immune response remains a central determinant of clinical outcome following SARS-CoV-2 infection and vaccines now provide an approach for pandemic control. The National Core Study - Immunity (NCSi) programme in Phase 0 was designed to co-ordinate and build on UK investment in COVID-19 immunity and initiated a number of investments in 2020/21. These were based on four themes which seek to predict and manage individual risk, protect acute infection and late effects, prevent primary or re-infection and prepare for future pandemic challenges. In Phase 1, these will continue and comprise: PREDICT: 1. Centre for Cytokine Autoantibodies will interrogate serum sample collections, including those from the NCSi/UKB collaboration, to determine the clinical importance of antibodies against a range of cytokines in order to define clinical risk and develop new therapeutic opportunities. 2. DIRECT: Determining the Immune Response in Ethnic minority healthcare workers to COVID-19 infecTion will determine the importance of ethnicity in relation to immune response to natural infection and post-vaccination. 3. EVITE study of shielding efficacy through evaluation of NHS records, questionnaire responses and blood test results at 12 months after shielding and subgroups such as those with cancer, BAME or living in deprived communities. 4. Asymptomatic COVID19 in Education (ACE) Immunity Study will examine SARS-CoV2 across the (young) population to influence student/school movement policies PROTECT: 1. NCSi collaboration with UK Biobank will undertake detailed analysis of Covid-specific immune responses and cellular phenotype in a world-leading unique 3000 participant repeat-imaging study. 2. Understand Immune senescence and its impact on natural immunity and vaccine responses in the CAIRO vaccine cohort and associated studies of vaccine response in secondary immune suppression with chronic lymphocytic leukaemia that is seen in older people. PREVENT: 1. Next Generation Immune Assays will be commissioned to transform the sensitivity, specificity and logistics of serological and cellular assays. 2. Vaccine Responses: The OCTAVE study of immune monitoring after vaccination will be maintained and supported with further investment. Phase 1 investment circa £1.1m, 75% funded by UKRI and 25% funded by the Vaccine Task Force. For more details please see https://www.ukri.org/news/new-study-tests-third-jab-for-people-with-weakened-immune-systems/ 3. Re-infection, vaccine failure and viral Variants of Concern will comprise a portfolio of studies including an open commissioned call to determine mechanisms of inadequate immune protection in (re-) infection after natural or vaccine-induced immunity.

Publicationslinked via Europe PMC

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

Risk of COVID-19 death in adults who received booster COVID-19 vaccinations in England.

Accelarated immune ageing is associated with COVID-19 disease severity.

Enhancement of Omicron-specific immune responses following bivalent COVID-19 booster vaccination in patients with chronic lymphocytic leukaemia.

VarLOCK: sequencing-independent, rapid detection of SARS-CoV-2 variants of concern for point-of-care testing, qPCR pipelines and national wastewater surveillance.

Risk of severe COVID-19 outcomes after autumn 2022 COVID-19 booster vaccinations: a pooled analysis of national prospective cohort studies involving 7.4 million adults in England, Northern Ireland, Scotland and Wales.

Long COVID research: an update from the PHOSP-COVID Scientific Summit.

Assessing neutrophil-derived ROS production at the bedside: a potential prognostic tool in severe COVID-19 cases.

Impact of COVID-19 on immunocompromised populations during the Omicron era: insights from the observational population-based INFORM study.