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

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View all publications at 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.