Single-cell studies on hapten-specific B cells: response to T-cell-dependent antigens.

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Abstract
The effectiveness of the hapten-gelatin antigen-affinity fractionation technique, for selection of hapten-specific B cells activatable by T-cell-dependent (TD) stimuli, was assessed. Normal adult murine spleen cells were fractionated on fluorescein (Flu)-gelatin layers, and the adherent cells were cultured singly or in small numbers with various sources of syngeneic keyhole limpet hemocyanin (KLH)-primed T lymphocytes. Conditions were defined under which the addition of Flu-KLH caused optimal clonal proliferation and differentiation of B cells into anti-Flu, directly hemolytic, plaque-forming cells (pfc). It was found that 3-5% of the Flu-specific B cells could be activated vs. 1 in 5000 unfractionated spleen cells. The mean enrichment factor for fractionation was 179, almost identical to that seen when the stimulus is T-cell-independent (TI), showing that the method is capable of isolating B cells responsive to antigenic stimuli requiring specific T-cell help. Efforts were made to determine whether TD B cells constituted a separate population from TI B cells by determining: clone frequencies using Flu-KLH, the TI antigen Flu-polymerized flagellin (Flu-POL) or a mixture of both for stimulation. With Flu-POL alone, and with the mixed stimulus, 2-3 times more pfc clones were produced than with Flu-KLH; yet evidence for separate B-cell subsets was not obtained because of strong bystander stimulation, due to the presence of the carrier-primed T cells in a confined volume of 10 .mu.l.