Page 844 - Veterinary Immunology, 10th Edition
P. 844

In disease caused by toxigenic bacteria such as clostridia or Bacillus
  VetBooks.ir  anthracis, the immune response must not only eliminate the

               invading bacteria but also neutralize their toxins. Destruction of the
               bacteria, however, may be difficult if they are embedded in a mass

               of necrotic tissue, and toxin neutralization is a priority.
               Neutralization occurs when antibody prevents the toxin from
               binding to its receptors on a target cell. The neutralization process
               therefore involves competition between receptors and antibodies

               for the toxin molecule. Once a toxin has bound to its cell receptors,
               antibodies are relatively ineffective in reversing this combination.



               Immunity to Invasive Bacteria

               Protection against invasive bacteria is usually mediated by

               antibodies directed against their surface antigens. Efficient
               phagocytosis requires that the bacteria be coated with opsonins that
               can be recognized by phagocytic cells. These opsonins include

               antibodies and C3b in addition to the innate opsonins such as
               mannose-binding lectin. Antibodies not only are effective opsonins
               in their own right but also increase the binding of C3b by activating
               the classical complement pathway. Antibodies directed against
               capsular (K) antigens may neutralize the antiphagocytic properties

               of bacterial capsules, thus permitting their destruction. In bacteria
               lacking capsules, antibodies directed against O antigens act as
               opsonins. Protection also results when antibodies are produced

               against the E. coli pilus antigens F4 (K88) and F5 (K99). The
               antibodies may interfere with the expression of pili. Once the
               adherence pili are suppressed, these strains of E. coli cannot bind to
               the intestinal wall and thus are no longer pathogenic.
                  The importance of bacterial capsules in pathogenesis is seen in

               anthrax. B. anthracis possesses both a capsule and an exotoxin.
               Antitoxic immunity is protective but slow to develop. In addition,
               toxin production tends to be prolonged since the organism is

               encapsulated and phagocytic cells have difficulty eliminating it. As
               a result, death is usually inevitable in unvaccinated animals. The
               vaccine commonly employed against animal anthrax contains an
               unencapsulated but toxigenic strain of B. anthracis. Given in the
               form of spores that can germinate, the unencapsulated bacteria are






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