Roadmap for the development of candidate vaccines for FMD
Download FMD Vaccine Roadmap11
Vector
Dependencies
Next steps
- 7 Vectored vaccines
- 7A Safety
- 7B Delivery route
- 7C Delivery platform
- 7D Efficacy in challenge model
Research Question
What are we trying to achieve and why? What is the problem we are trying to solve?
The development of safe vectors to be used for producing safe, effective, cross-reacting DIVA vaccines for FMD
Research Gaps and Challenges
What are the scientific and technological challenges (knowledge gaps needing to be addressed)?
- Prevent the development of immune responses to the vector
- Ensure the expression of the protective antigens by a replicating organism with the development of VN-Abs and
CTC responses - Create stable genetically modified organisms expressing the desired FMD antigens
- Identify the Ag combination to give widest protection against the various field isolates
Solution Routes
What approaches could/should be taken to address the research question?
- Generation of genetically modifies organisms (viruses or bacteria) expressing the protective antigens of different
FMDV strains - Incorporation of molecular adjuvants
Dependencies
What else needs to be done before we can solve this need?
Identity of protective antigens
State Of the Art
Existing knowledge including successes and failures
Replication-defective human adenovirus type 5 (Ad5) vectors that contain the capsid-encoding regions of FMD virus
(FMDV) are currently used and are promising in terms of efficacy, cross reaction and safety.
Projects
What activities are planned or underway?
spatial model of foot and mouth disease outbreak in an endemic area of thailand
Planned Completion date 01/10/2021
Netherlands
Epidemiology of foot-and-mouth disease outbreaks in Thailand from 2011 to 2018
Planned Completion date 01/11/2022
Netherlands