Highly enriched preparations of human CD3 + CD4 + T-lymphocytes were stimul
ated with mitogen or OKT3 to determine the capacity of K-562 cells to funct
ion as accessory cells. Phorbol 12-myristate 13-acetate (PMA)-treated K-562
cells were induced to differentiate along the megakaryocytic lineage and c
ould supplant monocyte-accessory cell function. Intracytoplasmic analysis o
f interleukin-4 (IL-4) and interferon-gamma (IFN-gamma) established that IL
-4, and not IFN-gamma, was preferentially produced by the activated lymphoc
ytes. This polarized stimulation is compatible with a type 2 or humoral imm
une response of purified T cells co-cultured with differentiated K-562 cell
s in vitro, and may have implications in immunoregulation due to disease pr
ogression. (C) 2000 Elsevier Science Ltd. All rights reserved.