The T cell-secreted lymphokine interleukin 13 (IL-13) exerts pleiotropic ef
fects on monocytes (M phi) and B cells. Since accessory cells, like M phi a
nd B cells, also act in antigen-presenting and lymphokine augmentation of T
cells, M phi and B cells may be able to effect T cell IL-13 production. Pu
rified T cells produced slightly less IL-13 than the lower T cell numbers c
ontained in peripheral blood mononuclear cell population, further suggestin
g accessory cell augmentation. Addition of 10% B cells [either unstimulated
or pokeweed mitogen (PWM)-stimulated] to autologous T cells only moderatel
y augmented T cell IL-13 levels, PWM-stimulated B cell culture supernates h
ad even less augmenting effect on T cell IL-13 levels and unstimulated B ce
ll culture supernates did not augment T cell IL-13 production. In contrast
to the moderately augmenting effect of B cells or their stimulated culture
supernates, addition of 10% M phi, either unstimulated or muramyl dipeptide
(MDP)+ IFN-gamma stimulated, to autologous T cells produced a highly signi
ficant increase in T cell IL-13 production, M phi culture supernates were e
qually effective in augmenting T cell IL-13 levels, suggesting both that ce
ll-to-cell contact is not critical for M phi augmentation of T cell IL-13 l
evels, and that M phi secreted factors are pivotal. CD64(+) M phi (or their
culture supernates), which are known as poor antigen-presenting cells, als
o effectively augmented T cell IL-13 production, further supporting the inv
olvement of M phi secreted factors, Finally, experiments with exogenous add
ition of recombinant monokines, as well as neutralization experiments with
different cytokine antibodies, suggested IL-1 beta as a primary cytokine in
volved in the augmentation of T cell IL-13 levels by accessory cells. Howev
er, these experiments also indicated other unidentified M phi factors as pl
aying a significant role in producing maximal T cell IL-13 production. (C)
1998 Academic Press.