Page 862 - Veterinary Immunology, 10th Edition
P. 862

VetBooks.ir  Some Antibacterial Vaccines





               Toxoids


               The immunoprophylaxis of tetanus is restricted to toxin
               neutralization. Tetanus toxoid in an aluminum hydroxide
               suspension is given for routine prophylaxis, and a single injection

               will induce protective immunity in 10 to 14 days. Conventional
               immunological wisdom would suggest that the previous use of
               tetanus immune globulin should interfere with the immune
               response to toxoid and must therefore be avoided. This is not a
               problem in practice, however, and both may be successfully

               administered simultaneously (at different sites) without problems.
               This may be because of the relatively small amount of immune
               globulin usually needed to protect animals.

                  Some veterinary vaccines combine both toxoid and killed bacteria
               in a single dose by the simple expedient of adding formaldehyde to
               a whole culture. These products, sometimes called anacultures, are
               used to vaccinate against Clostridium haemolyticum and C.
               perfringens. Trypsinization of the anaculture may make it more

               immunogenic. Toxoids, usually incorporated with an alum
               adjuvant, are available for most clostridial diseases and for
               infections caused by toxigenic staphylococci.



               Bacterins


               Vaccines containing killed bacteria are called bacterins. It is usual to
               kill the bacteria with formaldehyde and to add alum or aluminum
               hydroxide adjuvants. As with other dead vaccines, the immunity

               produced by bacterins is relatively short lived, usually lasting no
               longer than 1 year and sometimes considerably less.
                  Bacterins may be improved by adding purified immunogenic
               antigens to the killed bacteria. E. coli bacterins against enteric

               colibacillosis may be enriched and made much more effective by
               the addition of K88 or K99 pilus antigens. Antibodies to these
               antigens block E. coli binding to the intestinal wall and thus
               contribute to protection. Similarly, Mannheimia bacterins enriched






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