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| **Virulent organisms cannot be used as vaccines as they would cause disease | | **Virulent organisms cannot be used as vaccines as they would cause disease |
| **Virulence is reduced by growing the organism in altered conditions so that it is less able to replicate when introduced to the host and therefore less likely to cause disease | | **Virulence is reduced by growing the organism in altered conditions so that it is less able to replicate when introduced to the host and therefore less likely to cause disease |
| + | **Produces a superior response to disease than using killed organisms as the dose of antigen is larger and more sustained |
| + | **Response takes place at site of natural infection producing a greater local response than with killed organism vaccines |
| | | |
| *Killed inactivated organism or toxin (toxoid) | | *Killed inactivated organism or toxin (toxoid) |
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| **The gene for the antigen required is inserted into a virus vector or cloned into bacteria | | **The gene for the antigen required is inserted into a virus vector or cloned into bacteria |
| **Small antigens, such as peptides can be synthetically produced | | **Small antigens, such as peptides can be synthetically produced |
| + | **E.g. being developed constantly to fight the Inflenza viruses |
| | | |
| *DNA coding for proteins (antigens) | | *DNA coding for proteins (antigens) |
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| **E.g. Aluminium salts generate bias T helper II responses for '''antibody'''-mediated immunity | | **E.g. Aluminium salts generate bias T helper II responses for '''antibody'''-mediated immunity |
| **E.g. Killed mycobacteria generate IL-12 producing good '''cell'''-mediated immunity | | **E.g. Killed mycobacteria generate IL-12 producing good '''cell'''-mediated immunity |
| + | |
| + | *Adjuvants decrease the number of injection needed and the amount of antigen administered |
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| ==Which type of vaccine is used for each disease?== | | ==Which type of vaccine is used for each disease?== |