Vaccine Induced Immunity in the Young and Aged

  • Funded by National Institutes of Health (NIH)
  • Total publications:5 publications

Grant number: 3U19AI057266-17S1

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2020
    2023
  • Known Financial Commitments (USD)

    $506,680
  • Funder

    National Institutes of Health (NIH)
  • Principal Investigator

    RAFI AHMED
  • Research Location

    United States of America
  • Lead Research Institution

    EMORY UNIVERSITY
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Immunity

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Adults (18 and older)Older adults (65 and older)

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

The over-arching goal of this proposal is to analyze SARS-CoV-2 antibody seroconversion rates in healthcare workers at the Emory University Hospital over the next year and to study adaptive immune responsesto SARS-CoV-2 infection during acute infection and at convalescence. These studies will draw on threemain sources of samples, either through an emerging infectious disease protocol at the Emory VaccineCenter Hope Clinic, through a sero-surveillance study initiated at Emory, and previously collected PBMCand serum samples from adult or elderly donors by Dr. Jorg Goronzy, respectively. We will develop andemploy a combination of antibody binding assays and viral neutralization assays to test the quantity andquality of the infection-induced antibody responses. This information will also be used to identify optimaldonors for single-cell antibody expression cloning, as we have previously described9-13. A recentlypurchased 10x instrument in our BSL3 facility at the Emory Vaccine Center will allow for a detailed analysisof the transcriptional profiles of innate and adaptive immune responses during acute SARS-CoV-2infection. The proposed studies will provide key insight into the dynamics of this devastating diseaseamong health care workers at a major metropolitan hospital in Atlanta. These efforts will also generate keyserological tools, provide an understanding of the humoral immune response to SARS-CoV-2 infection,and generate human monoclonal antibodies, with both diagnostic and therapeutic potential.

Publicationslinked via Europe PMC

Neutralization against BA.2.75.2, BQ.1.1, and XBB from mRNA Bivalent Booster.

Rapid Detection and Characterization of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Omicron Variant in a Returning Traveler.

Infection and Vaccine-Induced Neutralizing-Antibody Responses to the SARS-CoV-2 B.1.617 Variants.

Evaluation of Cellular and Serological Responses to Acute SARS-CoV-2 Infection Demonstrates the Functional Importance of the Receptor-Binding Domain.

A yeast expressed RBD-based SARS-CoV-2 vaccine formulated with 3M-052-alum adjuvant promotes protective efficacy in non-human primates.