DNA-based delivery of antiviral antibodies for Zika and Influenza prevention
- Funded by Wellcome Trust
- Total publications:0 publications
Grant number: 228129/Z/23/Z
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Key facts
Disease
Zika virus disease, UnspecifiedStart & end year
20242025Known Financial Commitments (USD)
$2,881,210.94Funder
Wellcome TrustPrincipal Investigator
Dr. Rachel A LiberatoreResearch Location
United States of AmericaLead Research Institution
RenBioResearch Priority Alignment
N/A
Research Category
Therapeutics 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
RenBio proposes a two-pronged approach to evaluate the applicability of MYO Technology for DNA-based antiviral antibody delivery, using antibodies directed against Zika virus (ZIKV) and influenza A virus (IAV). The MYO Technology platform uses intramuscular electroporation to efficiently deliver antibody-encoding plasmid DNA to muscle cells, which then produce and secrete the antibody, delivering it to systemic circulation. Multiple proof-of-concept animal studies, including an IAV challenge study, have demonstrated efficacy with this approach, which has the potential to greatly improve access to antibodies by reducing costs and dosing frequency. The two aims of this proposal are to 1) complete IND-enabling preclinical activities to support the development of a potent anti-ZIKV antibody, and 2) evaluate the potential for the delivery of cocktails of anti-IAV antibodies for the prevention of disease. The first aim would complement an ongoing program partially funded by the US government via the Defense Advanced Research Projects Agency and conducted in collaboration with academic partners. The second aim would result in an assessment and mitigation of technical hurdles associated with DNA-based delivery of antibody cocktails, with proof-of-concept data generated in animal models of IAV infection. These two aims have the potential to significantly impact ZIKV and IAV disease prevention.