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Antivirals. Anti HIVReverse transcriptase inhibitorsProtease inhibitorsFusion inhibitorsAnti HBV3TC. Antivirals. Anti HCVInterferon/ribavirinAnti InfluenzaFusion inhibitors: oseltamivir (Tamiflu)Cleavage inhibitors: amantadine, rimantadine Ribavarin general antiviral mixed success, tox
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1. Importance of vaccination for viral diseases Unlike bacterial infections where antibiotics are in general effective (although there is an increasing problem of resistance),
there are few effective and safe antivirals, emphasising the need for effective vaccines.
2. Antivirals
Anti HIV
Reverse transcriptase inhibitors
Protease inhibitors
Fusion inhibitors
Anti HBV
3TC
3. Antivirals Anti HCV
Interferon/ribavirin
Anti Influenza
Fusion inhibitors: oseltamivir (Tamiflu)
Cleavage inhibitors: amantadine, rimantadine
Ribavarin general antiviral
mixed success, toxicity problems
4. Primary/secondary immune response The aim of vaccination is to mimic the effect of the primary infection in the absence of disease and prime the appropriate immune response (both antibody IgG/A and T-cell).
When the virus is encountered there is a more rapid and larger immune response which limits virus replication and spread and clears the virus prior to the initiation of disease.
5. Purpose of vaccination Classically the aim of vaccination is to prevent disease not necessarily infection.
This is satisfactory for an acute infection such as measles.
Not necessarily adequate for viruses, such as HIV or HSV, which establish latent/persistent infections probably in the absence of replication.
6. Herd immunity If a certain % of the population is vaccinated (typically 90+%), unvaccinated individuals will also be protected as the virus will not have a large enough reservoir to spread rapidly through the population. This is partly the aim of large school/community based vaccination programmes.
Studies with influenza vaccination have demonstrated that the most effective way to protect elderly patients in residential care is to vaccinate the health care workers and thus prevent them infecting their patients. Partly because the ability to mount an immune response to vaccination (and infection) falls with age.
7. Live versus inactivated vaccines (1) Live attenuated viruses replicate to a limited extent
Mimic natural infection
Only 1 dose usually required
Lower dose
Antibody response: both serum IgG and if appropriate a mucosal IgA
More likely to prevent initial infection
T-cell response
Potential to revert to pathogenic virus
Less stable
8. Live versus inactivated vaccines (2) Killed vaccines do not replicate
High dose with booster injections required
Only serum IgG response
Problem of incomplete inactivation
Generally stable as only protein
9. Live attenuated vaccines Polio Sabin strains
Vaccinia
Measles
Mumps
Rubella
Varicella-zoster
10. Inactivated vaccines Polio Salk strains
Hepatitis A
(Hepatitis B)
Rabies
Yellow fever
Influenza
11. MMR Vaccination Indications
All children in the second year of life
Booster at school entry
Important for long lasting immunty
Administration
1 dose of live attenuated MMR
Protection
Evidence that immunity wanes
Surveillance important