Page 670 - Veterinary Immunology, 10th Edition
P. 670

dendritic cells can extend their processes into the intestinal lumen
  VetBooks.ir  and sample the microbiota. These bacteria can persist within the

               dendritic cells for several days while the cells carry them into the
               mucosa and mesenteric lymph nodes and present them to B cells. In

               addition, some bacteria are taken up by specialized antigen-
               capturing M cells, penetrate the Peyer's patches, and become
               resident within the tissues. Although most of these invading
               bacteria are killed by macrophages, some are also presented to B

               cells. The B cells produce IgA, which may modify the composition
               of the microbiota and block further mucosal penetration. Bacteria
               are thus prevented from breaching the mucosal barrier by the
               ongoing IgA response, and the mesenteric lymph nodes form an

               additional barrier that prevents the commensals from reaching the
               systemic immune system. It is likely that a similar local IgA
               response occurs against food antigens. (The role of IgA is discussed
               in detail in Chapter 22.)



               T Cell Functions


               The intestinal immune system must be relatively unresponsive to
               the microbiota while still being able to respond to potential
               pathogens. Thus it must be highly regulated. The key to successful

               accommodation with the intestinal microbiota depends on the
               body's ability to control inflammation in the gut wall. This is
               achieved by a maintaining a balance between proinflammatory

               Th17 cells and antiinflammatory Treg cells (Fig. 21.9).
































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