AbstractIn the present studies, we compared the activation requirements of sIgM+/sIgD+B cells with those of isotype‐switched sIgM−/sIgA+B cells. We found that whereas sIgM+B cells respond to T cell‐independent (TI) and T cell‐dependent (TD) Ag with no significant bias toward one stimulus, sIgA+B cells were deficient in their ability to respond to antigen receptor cross‐linking but responded remarkably well to TD stimuli. Thus, dextran‐conjugated anti‐IgA antibody (anti‐IgA‐dextran), anti‐kappa‐dextran, or various immobilized anti‐IgA antibodies (Ab) induced only low‐level IgA B cell proliferation and no IgA secretion in the presence of various lymphokines; in marked contrast, sIgA+B cells responded to cognate and noncognate T cell stimulation as well as to stimulation by CD40 ligand‐bearing fibroblasts by secreting large amounts of IgA (up to 240 000 ng/ml per 105cells). This pattern of sIgA+B cell responsiveness was noted with both germinal center peanut agglutininhi(PNAhi) and non‐germinal center PNAloB cells. In confirmation of these results, whole Peyer's patch or lamina propria cell populations containing less than 15 sIgA+B cells stimulated with a noncognate T cell stimulus or T cell membranes secreted mainly IgA (68–94 of the total Ig secreted) and relatively little IgM. The strict T cell dependence of IgA B cell activation and differentiation provides important insights into immune responses of mucosal tissues and must be considered in the development of vaccines, particularly those designed to stimulate mucosal tissues containing large numb
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