Abstract
Mice were primed with dinitrophenyl (DNP) (trinitrophenyl, TNP) coupled to thymus-independent (TI) or thymus-dependent (TD) carriers. B [bone marrow-derived] cells from these mice were transferred to irradiated recipients with T [thymus-derived] cells from keyhole limpet hemocyanin (KLH)-primed mice. After secondary immunization with DNP-KLH a significant DNP-specific Ig[immunoglobulin]G memory response was produced only by mice which received B cells which were primed with TD antigens. TI antigens were unable to induce differentiation of B-cell precursors to IgG producing memory B cells but they did not suppress the induction of B-memory cells by TD antigens. TI antigens probably fail to activate a cell type which is required for the induction of memory B cells.

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