Rapid Development and Initial Preclinical Evaluation of an Effective Candidate Vaccine against SARS-CoV-2

  • Funded by Luxembourg National Research Fund
  • Total publications:0 publications

Grant number: unknown

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Key facts

  • Disease

    COVID-19
  • Known Financial Commitments (USD)

    $54,000
  • Funder

    Luxembourg National Research Fund
  • Principal Investigator

    Markus Ollert
  • Research Location

    Luxembourg
  • Lead Research Institution

    Luxembourg Institute of Health (LIH)
  • Research Priority Alignment

    N/A
  • Research Category

    Vaccines research, development and implementation

  • Research Subcategory

    Pre-clinical studies

  • Special Interest Tags

    Innovation

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

The current pandemic caused by severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) is a threat not only to global health but also to the economy since it is dramatically affecting the socio-economic layers of societies around the planet. Thus, it will be critically important to advance in the production of an effective vaccine, which will be crucial for building up sufficient population-based immunity to efficiently curb the pandemic. While SARS-CoV-2 can infect everyone at all ages, it is mainly the elderly population that is most at risk of a fatal outcome. Elderly persons are characterized by a declining immune function, known as immuno-aging. To address this specific challenge, vaccines against SARS-CoV-2 that specifically protect not only younger people but also the elderly are urgently needed. We propose a project for vaccine development against SARS-CoV-2 based on expression of recombinant SARS-CoV-2 antigenic variants in a novel trimeric form and combine the antigen delivery with the adjuvant activity of CpG oligodinucleotides. CpG adjuvant is known as an already FDA-approved vaccine adjuvant that confer strong immune responses in young and elderly persons. After 6 months, we will deliver an optimized lead antigen vaccine candidate that will already be pre-clinically evaluated for robust induction of virus-neutralizing immunity in mice.