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          is also required for full activation of those   embryonic development. In birds, lym-
                                                  phoid cells destined to become B cells leave
          cytotoxic T cells. The activated cytotoxic T
  VetBooks.ir  cells also undergo a series of cell divisions to   the bone marrow and travel to the bursa of
                                                  Fabricius, which is similar to the thymus
          provide increased numbers of the selected
          clone and also produce a subset to serve as   but associated with the intestinal tract.
          memory cells (memory T  cells). Activated   Here the cells undergo maturation and
                                C
          cytotoxic cells (killer cells) destroy cells bear-  selection similar to that which happens to
          ing the antigen for which they were selected.   pre‐T cells in the thymus. Mature B cells
          Physical  contact  and  binding  between  the   leaving the bursa in birds also populate
          cells bearing the antigen and the cytotoxic T   peripheral  lymphoid  structures,  and  it  is
          cells are required for the destruction of anti-  these structures that produce B cells in
          gen‐bearing cells (Fig. 16‐1), and secretions   adult birds. An organ that is the functional
          from the cytotoxic T cells, including per-  equivalent to the bursa has not been iden-
          forin to disrupt the cell membrane of the   tified in mammals. It is thought that B cells
          antigen‐bearing cells, accomplish it.   mature in the bone marrow in mammals
                                                  and leave the marrow to populate the
                                                  peripheral lymphoid structures. As with T
          Lymphocyte Origin,                      cells, the peripheral lymphoid structures
          Development, and Residence              produce B cells in adult animals. The
                                                  development of NK cells probably occurs
          Just as all lymphocytes are originally   in a manner similar to that for B cells.
          derived from pluripotent  stem cells  that
          subsequently became lymphoid stem cells
          in the bone marrow (see Fig.  15‐1), the   Active and Passive Immunities
          three general classes of lymphocytes (B
          cells, T cells, and NK cells) are all derived   Active immunity is a state of immunity to a
          from lymphoid stem cells.               specific antigen achieved by the response of
            The differentiation of lymphoid stem   one’s own immune system. Active immu-
          cells to the types of mature lymphocytes   nity may include both humoral and cell‐
          begins early during embryonic develop-  mediated responses. Passive immunity is a
          ment. Cells destined to become T cells   state of temporary immunity achieved by
          leave the bone marrow and travel to the   the transfer of immunoglobulins or T cells
          thymus, where secretions called  thymic   from an animal with active immunity to
          hormones act on them. These are not     another that has not encountered the anti-
            classic hormones, for they are local to the   gen involved. Passive immunity is a tempo-
          thymus, and lymphocytes must come to    rary state because the immunoglobulins
          the thymus to be acted on. The thymic   and/or T cells are degraded or destroyed
          hormones guide the further development   over time. Passive immunity is important in
          of the lymphocytes to become T cells. As   neonates that utilize immunity from the
          part of the development in the thymus,   dam while their own immune system is too
          only T cells capable of recognizing foreign   immature to provide active immunity.
          antigens are selected to survive. The
          selected T cells that leave the thymus pop-
          ulate lymphoid structures throughout the   Immunological Surveillance
          body, including tonsils, lymph nodes, the
          spleen, and collections of lymphocytes in   NK cells and cytotoxic T lymphocytes (killer
          the intestinal wall. These structures are   cells) both recognize and destroy cells with
          responsible for producing T cells in adult   foreign antigens in their membranes. Cancer
          animals (discussed later).              cells have surface antigens that are not
            Lymphoid stem cells destined to become     present in normal cells and thus can be rec-
          B cells also undergo differentiation during   ognized as foreign. It is believed that cancer
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