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Line 18: |
| **E.g. Canine Parvovirus | | **E.g. Canine Parvovirus |
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− | *To prevent the spread of disease | + | *To prevent the spread of disease by virus excretion |
| **E.g. Rabies, FMDV | | **E.g. Rabies, FMDV |
| + | |
| + | *The goal is to vaccinate 90% of the population to reduce the amount of '''endemic''' virus until no new infections occur |
| + | |
| + | *Once the disease risk is low, vaccination can be replaced by an eradication or quarantine programme |
| + | |
| + | ==How do vaccines work? |
| + | |
| + | *Vaccination sets up memory to the viral infection |
| + | |
| + | *High levels of cytotoxic T cells and neutralising antibody are activated in 1-2 days as a secondary response (instead of 4-10 days as a primary response) |
| + | |
| + | *The infection is therefore prevented from taking hold causing lesions to develop |
| + | |
| + | *Neutralising antibody blocks the attachment of virus to host cells receptors |
| + | |
| + | *'''Endogenous vaccines''' are where the antigen are made as new proteins by the cell, bacterium or virus |
| + | **Involves MHC class I processing |
| + | **E.g. live virus, recombinant virus and DNA vaccines |
| + | |
| + | *'''Exogenous vaccines''' are when the antigen is processed from the outside by endocytosis without any new proteins being made by the host cell |
| + | **involves MHC class II processing |
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| ==How do we vaccinate?== | | ==How do we vaccinate?== |