Page 629 - Veterinary Immunology, 10th Edition
P. 629

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                                 FIG. 20.12  The origins and properties of interleukin-10.


                  Oral administration of an antigen may induce pTreg cells. Treg
               cells from the mesenteric lymph nodes of orally tolerant animals
               secrete TGF-β, IL-4, and IL-10. This may account, in large part, for
               tolerance to food antigens.

                  Treg cells are not the only way in which cellular control of
               immune responses is exercised. Many of the regulatory activities of
               T cells reflect the antagonistic functions of Th1 and Th2 cells. For

               example, IFN-γ from Th1 cells can suppress IgE production,
               whereas IL-10 from Th2 cells is suppressive for dendritic cell IL-12
               production and thus for the production of Th1 cytokines.
                  In cattle, γ/δ T cells are a major regulatory T cell subset in
               peripheral blood. They spontaneously secrete IL-10 and proliferate

               in response to IL-10 and TGF-β. They can inhibit both antigen-
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               specific and nonspecific proliferation of CD4  and CD8  T cells in
               vitro.
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                  In horses, Tregs are FoxP3 , CD4 , and CD25 . They act in a
               manner similar to other species by cell-cell contact and by IL-10 and
                                                                                      +
               TGF-β production. As in humans the circulating CD4  CD25                        hi
               population contains tTreg cells, while pTreg cells can be induced in
               vitro by appropriate stimulation.

                                                             +
                                                   hi
                                         +
                  Pigs possess CD4  CD25  FoxP3  Tregs that produce
               immunosuppressive IL-10. They require IL-2 for activation, but
               excessive IL-2 may reduce their suppressive activity.




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