Page 927 - Veterinary Immunology, 10th Edition
P. 927

marked feature of visceral leishmaniasis, as described previously.
  VetBooks.ir  IgM-secreting cells so that very high levels of polyclonal IgM
                  Trypanosome infections may trigger an enormous increase in


               develop in the blood of infected animals. Some of these antibodies

               are directed against autoantigens. These include rheumatoid factor-
               like molecules, antibodies against thymocytes, single-stranded
               DNA, red cells, and platelets. The mechanism of this polyclonal B
               cell activation is unknown.

                  It is probable that a type IV hypersensitivity reaction contributes
               to the inflammation that occurs when Toxoplasma cysts break down
               and release fresh tachyzoites. Extracts of Toxoplasma gondii
               (toxoplasmin), if administered intradermally to infected animals,

               will cause a delayed hypersensitivity response (Chapter 33).



               Vaccination

               Successful vaccination against protozoan infections is currently

               limited to coccidiosis, giardiasis, leishmaniasis, babesiosis,
               theileriosis and toxoplasmosis.
                  Several live coccidial vaccines are given to poultry. These
               vaccines typically contain multiple species and strains of coccidia.
               Some consist of virulent, drug-sensitive organisms administered

               repeatedly in very low doses (trickle infection). Other vaccines have
               been attenuated by repeated passage through eggs, or they have
               been selected for precocity. Precocious strains mature very rapidly

               and, as a result, have less time to replicate and are thus less
               virulent. All of these vaccines provide solid immunity to coccidia
               when applied carefully under good conditions. Nevertheless, the
               dose of coccidia vaccine must be carefully controlled, and the
               vaccines must be harvested from the feces of infected birds.

               Vaccinated birds shed oocysts that are transmitted to other birds.
               Because of regional strain variation, vaccination may not be
               effective in protecting against field strains in all locations.

                  A vaccine is available to protect dogs and cats against Giardia
               duodenalis. The vaccine contains disrupted cultured Giardia
               trophozoite extracts administered subcutaneously and protects
               experimentally challenged dogs and cats against infection and
               clinical disease.






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