Page 457 - Veterinary Immunology, 10th Edition
P. 457

VetBooks.ir  Memory B Cells





               One reason that the primary immune response ends is that the
               responding B cells and plasma cells are simply removed by

               apoptosis. If all these cells died, however, immunological memory
               could not develop. Clearly some B cells must survive as memory
               cells. B cells are activated by antigen and helper T cells in the
               paracortex of lymph nodes. Most of these B cells differentiate into
               plasma cells and migrate to the bone marrow, spleen, and other

               organs, but some memory precursors remain in the cortex,
               proliferate, and form germinal centers. (Asymmetric division, as
               described above, likely accounts for these two different fates.) These

               cells persist under the influence of programming and rescue
               signals. Thus, memory cells are first screened for their ability to
               bind antigen. This induces CD154 on nearby T cells, which in turn
               promotes expression of bcl-2. Bcl-2 protects them against apoptosis
               and allows them to differentiate into memory cells.

                  Memory cells form a reserve of long-lived antigen-sensitive cells
               to be called on following subsequent exposure to an antigen. There
               are several classes of memory B cells distinguishable by their

               immunoglobulin class, their location, and their passage through
               germinal centers. For example, one population consists of small,
               long-lived resting cells with IgG BCR. These cells, unlike plasma
               cells, look like generic lymphocytes. Their survival does not depend
               on antigen contact. On exposure to antigen, they proliferate and

               differentiate into plasma cells without undergoing further
               mutation. It has been calculated that in a secondary immune
               response, the clonal expansion of memory B cells results in 8- to 10-

               fold more plasma cells than does a primary immune response.
                  A second memory B cell population consists of large, dividing
               cells with IgM BCR. These cells persist in germinal centers, where
               their continued survival depends on exposure to antigen on
               follicular dendritic cells. There are two distinct populations of

               plasma cells: a short-lived population that lives for 1 to 2 weeks and
               produces large amounts of antibodies shortly after antigen
               exposure, and a long-lived population that can survive for months

               or years. (In humans these plasma cells have a half-life of 8 to 15




                                                         457
   452   453   454   455   456   457   458   459   460   461   462