1. Generalities of Vaccination and Vaccine Formulations
The deliberate induction of active immunity to an agent by exposure to the agent or to non-replicating components, with the
intent of inducing protective immunity to challenge with a virulent infectious agent, is termed "vaccination". Actively acquired
immunity is that provided by an antigen specific response of the challenged host's own immune system in response to materials
recognized as non-self. Active immunity is usually long-lived with generation of memory cells. While we, as veterinarians,
will never be privy to all of the information due to proprietary protections, we can nonetheless develop rational strategies
for vaccine use based on the data we have. This data should be used to achieve the goals of maximizing the effective immune
response. By maximizing the immune response, the secondary goals of safety and cost can be met. Expectations a practitioner
should have in mind when choosing a vaccine formulation: First and foremost a vaccine should provide protection against virulent
challenge. Whether or not a vaccine actually does this, is at the heart of most of our vaccine conundrums and reflects the
degree to which a currently marketed vaccine has undergone efficacy testing (addressed in the next section). Second, a vaccine
must induce a protective immune response among essentially all members of a population. Premarketing efficacy testing should
demonstrate an efficacy level of at least 90-95% preventative activity. Many currently marketed vaccines do not provide this
level of efficacy overall or within target populations. Knowing these deviations from this goal is important for effective
vaccination. Third, a vaccine should induce memory for long-lasting protection. Most animal vaccines do have to show induction
of memory. Many are simple formulations that do not induce long-lasting protection. Fourth, a vaccine formulation should not
be susceptible to rapid evasion by strains of an infectious agent that vary antigenically from the type strain used in development
of the vaccine. We are fortunate in the equine industry to not have rapid expansion of new strains in many of our diseases,
even influenza. However, because of the regulatory barriers to frequent updating of vaccines, the industry is susceptible
to development of new strains of many diseases which could result in reemergence of disease. Fifth, it must be safe and without
serious side-effects. In the case of attenuated live vaccines, this includes no reversion to virulence. Sixth, vaccine use
should not cause confusion in the diagnosis of the active infection. Unfortunately vaccines are developed with little regard
to this expectation and frequently it is the diagnostic community that comes up with new testing strategies in response to
a vaccine. Seventh, vaccine should be stable and easy to transport. Unfortunately, for most veterinarians, this requirement
often leads to biasing of vaccine use only toward killed vaccines. Many killed vaccines are excellent, however, there are
other more recently developed vaccines that a far superior and the main barrier to their widespread use is the actual product
formulation. If this is the only barrier to use of a superior vaccine, then clients are ill-served. Eighth, the vaccine should
be affordable. The definition of affordability is ill-defined. If one chooses to use a shorter acting vaccine because it is
less expensive than a longer acting vaccine, then this is not a less expensive strategy for the client due to lack of protection
or the need for more frequent veterinary contact.
What a vaccine MAY NOT do is eradicate a disease. Eradication of disease through vaccination is a rare event. These diseases
generally have little subclinical or chronic states so that infected animals can be easily identified and separated from susceptible
populations: the best example is small pox vaccination. These diseases usually have a short incubation period and organism
spread is usually confined to the period of clinical signs. Eradicable diseases usually do not have wildlife reservoirs. Thus,
a serious discussion with clients on the expectation that vaccination will minimize disease but not erase the disease or totally
mitigate the risk of disease is required. An example of these are equine respiratory viruses. Vaccination against many of
the respiratory diseases, decrease severity of disease and decrease viral, but these common viruses will not eradicated through
vaccination.
In general a vaccine should NOT be used for treatment! There are many times during the incubation and onset of disease that
active priming of the immune response at that time is futile and may even be deleterious. For example, we have recently published
evidence that horses vaccinated against WNV within two weeks of exposure actually had a higher chance of exhibiting clinical
signs if they developed WNV within this time period (Rios LV. Et al. 2009)