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ABSTRACT
SIXTH FRAMEWORK PROGRAMME PRIORITY [SSP/8.1] [Policy-oriented Research
Priority]

STREP: SPECIFIC TARGETED RESEARCH OR INNOVATION PROJECT
| Project acronym: |
FMD ImproCon |
| Project full title: |
Improvement of Foot and Mouth disease control by ethically acceptable
methods based on scientifically validated assays and new knowledge
on FMD vaccines, including the impact of vaccination. |
| Contract SSPE No: |
503603 FMD ImproCon |
| Start Date: |
January 1st, 2004 |
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Project summary:
There is a strong desire to reduce reliance
on large-scale culling of animals to control future outbreaks of
FMD in EU Member States. As an alternative, it is proposed to use emergency
vaccination
and then to screen for residual infection using tests for antibodies
to the non-structural proteins of FMD virus. It is intended to amend
the
policy on FMD control to enable such an approach to be used in the
very near future. In reality, this means that current contingencies must
be
based on the use of existing vaccines. Therefore, this project seeks
to address the specific gaps in our knowledge and technological ability
with
respect to the implementation of a vaccinate-to-live policy. The
availability of adequate discriminatory diagnostic tests is the keystone
of the new
EU FMD control policy. The project is focused on the validation of
NSP-based tests to discriminate unequivocally between infected and vaccinated
animals,
in order to allow the implementation of the new policy in the immediate
term. Validation of existing and new NSP-tests as confirmatory tests
will be a major output of this project. The experimental design will
also provide
expected outputs in the field of the impact of vaccination on the
carrier state and on virus dissemination, the onset of vaccinal protection,
vaccine
potency in relation to emergency use, vaccine strain selection and
new marker vaccines. This project focuses on marker vaccines to induce
durable
protection against FMD. Conventional and marker vaccines will be targeted
to dendritic cells with particular attention to promote dendritic cell
mucosal homing (from parental immunisation), because mucosal immunity
can prevent FMD virus establishing local infection and the carrier status.
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