Immuno-Serological Assays for Monitoring COVID19 in Patients with Hematologic Malignancies

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

Grant number: 3U01CA260507-02S3

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2025
  • Known Financial Commitments (USD)

    $107,220
  • Funder

    National Institutes of Health (NIH)
  • Principal Investigator

    PROFESSOR Rong Fan
  • Research Location

    United States of America
  • Lead Research Institution

    YALE UNIVERSITY
  • 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

Summary The main goals of the Supplement Award are to (1) correlate immunoserological responses to early immune reactions in local tissue environment of the vaccine injection site in healthy donors, and (2) the compare between healthy controls and patients with hematological disorders or autoimmune disease. We will use a high plex immuno-fluorescence CODEX imaging panel to profile these skin biopsy samples in the next year of the award. Using this panel, we can confirm the expression of the SARS-CoV-2 Spike antigen. Interestingly, the SARS-CoV- 2 Spike antigen was detected in the epidermis and dermis of both arms from two donors. Specifically, SARS- CoV-2 Spike co-expressed with CD303 and CD63 of the unvaccinated arm tissue of a healthy donor and in cluster 0 of the vaccinated arm of a BCD donor, indicating expression in dendritic cells and basophils. In the next year to be supported by the Supplement Award, we will be imaging at least 13 more skin tissue sections and plan to conduct deeper informatics analysis. Additionally, we are performing DBiT-based spatial CITE-seq on adjacent slides from these 13 skin tissue sections and integrating the data with previously obtained sc-mRNA- seq data. Furthermore, we have completed immunoserology assays with the serum samples of these donors and patients. Therefore, once we complete the peripheral tissue spatial imaging and spatial omics sequencing, the results will be compared to systemic immunological and serological responses over times to help understand the role of early immune reaction in the development of an effective vaccine protection, in particular, in patients with blood cancer or autoimmune disease.