SARS-CoV-2 and serological responses in a South African birth cohort

  • Funded by Wellcome Centre for Infectious Diseases Research in Africa (CIDRI-Africa)
  • Total publications:239 publications

Grant number: Unknown

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2021
  • Known Financial Commitments (USD)

    $61,212.97
  • Funder

    Wellcome Centre for Infectious Diseases Research in Africa (CIDRI-Africa)
  • Principal Investigator

    Heather Zar
  • Research Location

    South Africa
  • Lead Research Institution

    University of Cape Town
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Immunity

  • Special Interest Tags

    N/A

  • Study Type

    Unspecified

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Children (1 year to 12 years)

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

The epidemiology of SARS-CoV-2 in children, spectrum of illness and risk factors are poorly understood. Further, recent data suggest that prior endemic coronavirus infection (nHCoV) may protect against SARS-CoV-2 infection or disease. We will leverage the Drakenstein Child Health Study birth cohort, capitalizing on a very well phenotyped population with high cohort retention, comprehensive longitudinal measurement of risk factors and a large biobank of samples, to prospectively investigate the epidemiology and risk factors for COVID-19 in children and serological responses (including false-positive testing with SARS-CoV-2 assays and cross-protective immunity). Further, since we have longitudinally documented infection with the four endemic coronaviruses in this cohort, we are uniquely placed to investigate the potential protective effect of nHCoV infection on SARSCoV-2. All children in the Drakenstein cohort (n=900) will have study visits at three timepoints (0, 3 and 6 months) to collect clinical and risk factor data and specimens (nasal and serum) for SARS-CoV-2 testing. Children with intercurrent illness will also have nasal, blood and an induced sputum specimen collected and tested. Risk factors for infection or disease will be collected, including environmental, nutritional, sociodemographic, maternal health, infectious exposures (including TB infection) and underlying illness. We will also test the most recent biobanked serum from each child collected before the COVID-19 epidemic (before March 2020) as well as selected biobanked convalescent serum samples from children with confirmed recent endemic (-229E, -NL63, -OC43, and -HKU1) coronavirus infection with serological tests for SARS-CoV-2, to investigate cross-reactive antibody responses and potential protection against SARS-CoV-2.

Publicationslinked via Europe PMC

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Cross-Activity Analysis of CRISPR/Cas9 Editing in Gene Families of <i>Solanum lycopersicum</i> Detected by Long-Read Sequencing.

Creating health systems citizens: enhanced professional identity formation through a para-curricular distinction track in health systems transformation and leadership.

A Comparison of Clinical Diagnostic Classification Criteria Used in Longitudinal Cohort Studies of the Alzheimer's Disease Continuum: A Systematic Review.

Identification and Characterization of a Rare Exon 22 Duplication in <i>CFTR</i> in Two Families.

Structural Rearrangement in Cyclic Cu(II) Pyridyltriazole Complexes: Oxidation of Dabco to Oxalate and CO<sub>2</sub> Conversion to Carbonate.

Administration of FOLFIRINOX for Advanced Pancreatic Cancer: Physician Practice Patterns During Early Use.