We have isolated two subtypes of helper T cells from human tonsils: CD4+ CD57+ cells,
mostly located in the germinal center (GC), and CD4+ CD57- cells, distributed through the
interfollicular areas but also present in the GC. In a functional study, we have compared the
capacities of these T-cell subtypes to stimulate B cells in cocultures. In order to block T-cell
proliferation while maintaining their activation level, we pretreated isolated T cells with
mitomycin C prior to culture in the presence of B cells and added polyclonal activators such
as PHA and Con A, combined or not with IL-2. Contrary to CD4+ CD57- cells,
CD4+ CD57+ cells did not markedly enhance B-cell proliferation. Even when sIgD-B cells
typical of germinal center cells were tested, the CD4 CD57 cells had no significant effect.
This is in accordance with the location of these cells: They mainly occupy the light zones
of the GC where few B cells divide. Even when added to preactivated, actively proliferating
cells, CD4+ CD57+ cells failed to modulate B-cell multiplication. On the supernatants of
B-cell-T-cell cocultures, we examined by the ELISA technique the effect of T cells on Ig
synthesis. Contrary to CD57- T cells, whose effect was strong, CD57+ T cells weakly
stimulated Ig synthesis. More IgM than IgG was generally found. Because CD57 antigen is
a typical marker of natural killer cells, we tested the cytolytic activity of tonsillar
CD4+ CD57+ cells on K562 target cells. Unlike NK cells, neither CD4+CD57+ nor
CD4+ CD57- cells exhibit any cytotoxicity. Thus, germinal center CD4+ CD57+ cells are not
cytolytic and do not strongly stimulate either B-cell proliferation or Ig secretion.
CD4+ CD57- cells, however, enhance B-cell proliferation and differentiation, thus acting
like the classical helper cells of the T-dependent areas.