Page 350 - Veterinary Immunology, 10th Edition
P. 350

antibody production is stimulated, the progeny of these B cells
  VetBooks.ir  move to the medulla and begin to secrete antibodies. Some of these

               antibody-producing cells may escape into the efferent lymph and
               colonize downstream lymph nodes. Several days after antibody

               production is first observed in the medulla, germinal centers appear
               in the cortex.
                  Some T cell–dendritic cell interactions are long-lasting, and in the
               presence of antigen, T cells and dendritic cells form stable

               complexes for many hours. However, before selecting its partner, a
               dendritic cell might sample as many as 500 different T cells/hour
               and can interact with up to 10 simultaneously (see Fig. 10.6).
                  Adherence to follicular dendritic cells is the predominant means

               of antigen trapping once an animal has been sensitized by previous
               exposure to an antigen. In a secondary response the germinal
               centers become less obvious as activated memory cells emigrate in
               the efferent lymph. Once this stage is completed the germinal

               centers redevelop.
                  Antigen-stimulated lymph nodes also trap lymphocytes.
               Interactions between infectious agents and mast cells result in the
               production of tumor necrosis factor-α (TNF-α). The TNF-α blocks

               the passage of lymphocytes through these organs, the lymphocytes
               accumulate, and the lymph nodes swell. This trapping concentrates
               lymphocytes close to sites of antigen accumulation. After about 24
               hours the lymph nodes release their trapped cells and their cellular

               output is increased for several days.


               Lymphocyte Circulation

               In adult animals, most cell types reside in stable tissues and do not
               move a lot. The many different cells of the immune system are, in

               contrast, highly mobile. Cells move from the bone marrow to the
               thymus and secondary lymphoid organs; cells migrate around the
               body looking for invaders and also move from lymphoid organs to
               sites of microbial invasion. T cells, for example, constantly circulate
               around the body in the blood and tissue fluid and are the

               predominant lymphocytes in blood (Fig. 12.15). As they travel, they
               survey the body for foreign antigens and preferentially home to
               sites of microbial invasion and inflammation.







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