Enhancing the Immunogenicity of a Tetravalent Dengue DNA Vaccine
Abstract
Dengue fever ranks among the top infectious diseases that afflict US Military personnel deployed overseas. Developing a successful vaccine to prevent dengue fever in DoD personnel is priority research area for the US DoD. Phase 1 clinical trials demonstrated that the Naval Medical Research Centers DNA based dengue vaccine is safe and well tolerated, but does not elicit a sufficient immune response. The objectives of this project are to conduct studies in non-human primates to enhance the immunogenicity of the vaccine by (a) testing different modes of delivery of dengue DNA vaccine for optimal humoral and T cell responses, and (b) testing the optimal delivery method in conjunction with other vaccine platforms using a heterologous prime-boost regimen. All necessary contracts are in place, the vaccine product is ready and the first vaccinations to address objective (a) are scheduled for early October 2016.
Document Details
- Document Type
- Technical Report
- Publication Date
- Aug 01, 2016
- Accession Number
- AD1020595
Entities
People
- Maya Williams
Organizations
- Henry M. Jackson Foundation for the Advancement of Military Medicine