immunogens, since they are so large and Killed Cell or Inactivated Virus complex. Depending on the vaccine, these are either killed or attenuated. Heat or Vaccine Administer stimulates Killed vaccines (viruses are termed “inactivated” chemicals immunity instead of “killed”) are prepared by cultivating Ags Dead, but but pathogen the desired strain or strains of a bacterium or antigenicity cannot multiply. is retained virus and treating them with chemicals, radiation, Whole microbes heat, or some other agent that does not destroy stimulate immunity Live, Attenuated Cells or Viruses but cause no antigenicity. The hepatitis A vaccine and three disease. forms of the influenza vaccine contain inactivated viruses. Because the microbe does not multiply, Virulence Administer killed vaccines often require a larger dose and is eliminated more boosters to be effective. or reduced. Ags Live attenuated vaccines contain live microbes Alive, with Vaccine microbes whose virulence has been attenuated, or lessened/ same antigenicity can multiply and eliminated. This is usually achieved by modifying boost immune stimulation. the growth conditions or manipulating microbial genes in a way that eliminates virulence factors. The advantages of live preparations are as follows: Vaccines for measles, mumps, and rubella contain 1. Viable microorganisms can multiply and produce infection (but not disease) like the natural live, nonvirulent viruses. organism. 2. They confer long-lasting protection. 3. They usually require fewer doses and boosters than other types of vaccines. 4. They are particularly effective at inducing cell-mediated immunity. Disadvantages of using live microbes in vaccines are that they require special storage facilities, can be transmitted to other people, and can mutate back to become virulent again.
Subunit Vaccines (Parts of Organisms)
If the exact epitopes that stimulate immunity are known, it is possible to produce a vaccine based Viruses Bacteria on a selected component of a microorganism. These vaccines for bacteria are called subunit vaccines. The antigens used in these vaccines may be taken from cultures of the microbes, produced by genetic engineering or synthesized chemically.
Examples of component antigens currently in Antigens
use are the capsules of the pneumococcus and stimulate meningococcus, the protein surface antigen of Genetically Engineered Antigens Toxoids immunity anthrax, and the surface proteins of hepatitis B but no pathogen virus. A special type of vaccine is the toxoid, is present. which consists of a purified bacterial exotoxin that has been chemically denatured. By eliciting Protein Toxin Toxoid the production of antitoxins that can neutralize Plasmid the natural toxin, toxoid vaccines provide containing foreign protection against diseases such as diphtheria, microbe antigen tetanus, and pertussis.