COVID Immunophenotyping Study

  • Funded by National Institutes of Health (NIH)
  • Total publications:0 publications

Grant number: 3R01AI132774-03S1

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2021
  • Known Financial Commitments (USD)

    $381,463
  • Funder

    National Institutes of Health (NIH)
  • Principal Investigator

    JANE HOYT BUCKNER
  • Research Location

    United States of America
  • Lead Research Institution

    BENAROYA RESEARCH INST AT VIRGINIA MASON
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Diagnostics

  • 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

This application is being submitted to PA-20-135 in accordance with NOT-AI-20-034. We are requesting anemergency supplement to R01AI32774 "Mechanisms of IL-6 mediated T cell pathogenesis in autoimmunity"(PI: Jane H. Buckner). This supplement will directly address the NOT-AI-20-034 research area of interest"Identification and evaluation of the innate, cellular and humoral immune response to SARS-CoV-2infection.....". Importantly, the proposed work is part of the NIAID Immunophenotyping assessment in aCOVID-19 Cohort (IMPACC) study tasked with performing longitudinal immunophenotyping from 1,000subjects with COVID-19. For each subject, among other assays, transcriptomic profiling will be done onperipheral blood, nasal swabs and endotracheal aspirates at six different time points. Specific to theemergency supplement requested here, we will be responsible for performing both the bulk host mRNA-sequencing (RNA-seq) and PCR quantification of viral nucleic acid from SARS-CoV-2 for each of the ~6,000anticipated nasal swab samples. In addition, we will perform a pilot study on 60 nasal swab samplesassessing the potential utility of metagenomic sequencing on these samples to consider it in a larger scale inthis cohort. All work will be done in close coordination with NIAID, University of California, San Francisco(endotracheal RNA-seq), Emory University (blood RNA-seq), and Icahn School of Medicine at Mount Sinai(virology) core sites.