1)MVA based SARS-CoV-2 vaccines
- Funded by National Institutes of Health (NIH)
- Total publications:0 publications
Grant number: 3R01AI148378-01S1
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Key facts
Disease
COVID-19Start & end year
20192023Known Financial Commitments (USD)
$102,106Funder
National Institutes of Health (NIH)Principal Investigator
Rama Rao AmaraResearch Location
United States of AmericaLead Research Institution
Emory UniversityResearch Priority Alignment
N/A
Research Category
Pathogen: natural history, transmission and diagnostics
Research Subcategory
Disease models
Special Interest Tags
N/A
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 overall goal of this proposal is to develop effective prophylactic vaccines against the novel SARSCoronavirus-2 (SARS-CoV-2) infection that has recently emerged as a pandemic across the world. The SARSCoV-2 has already infected more than 120,000 people and over 4000 people died due to COVID-19, a diseasecaused by SARS-CoV-2. Thus, there is an urgent need for the development of a vaccine that can rapidly induceanti-viral immunity and prevent infection. Previous data from other related coronavirus infections such as SARSCoV and MERS-CoV demonstrate that a strong neutralizing antibody response against the spike protein caneffectively prevent infection. Thus, a primary goal of this proposal is to develop a modified vaccinia Ankara (MVA)based vaccine that expresses SARS-CoV-2 spike protein to generate a rapid and strong neutralizing antibodyresponse both in systemic and mucosal compartments. There are several advantages to MVA based vaccinesthat include their excellent safety and a single dose of MVA vaccination can provide protection against multiplevirus infections including SARS-CoV, MERS, Zika and Ebola viruse. A novel aspect of this proposal is that wewill compare the immunogenicity and protective ability of different forms of the spike protein with a goal ofinducing neutralizing antibodies against both SARS-CoV-2 and SARS-CoV. This proposal has two specific aims.The goal of Aim 1 is to generate MVA vaccines and characterizing the anti-spike antibody response in mice. Wewill also compare parenteral (i.m.) vs mucosal (intranasal) vaccinations to determine the best route for inducingmucosal antibody response. The goal of Aim 2 is to evaluate the protective efficacy of the MVA-based SARSCoV2 vaccines. There is an urgent and unmet need to develop and characterize small animal models forevaluating vaccine efficacy against SARS-CoV2. Mice have served as an excellent model system to not onlyunderstand immunity to the related SARS virus but also for evaluating vaccines and antiviral therapeutics. In thisAim, we will develop and characterize a mouse model of SARS-CoV2 infection and use this model to test theprotective efficacy of our MVA-based vaccine candidates. The completion of these studies will not only providea mouse model for SARS-CoV2 infection but also develop vaccine candidates against SARS-CoV2.