CD1 molecules have recently been shown to present bacterial antigens t
o CD4(-)CD8(-)TCR alpha beta(+) T lymphocytes. The expression of CD1 o
n monocytes can be induced by GM-CSF and is further enhanced by IL-4.
GM-CSF and IL-3 receptors share a common chain and often have similar
activities; however, only IL-3, but not GM-CSF, can stimulate CD4(-)CD
8(-)TCR alpha beta(+) T lymphocytes directly, In this study we show th
at IL-3, in combination with IL-4, can also induce the expression of C
D1 on monocytes to a level comparable to that induced by GM-CSF/IL-4.
This induction of CD1 by IL-3 can be suppressed by IL-10. Furthermore
CD1-induced antigen presentation was similar whether CD1 was induced b
y IL-3/IL-4 or GM-CSF/IL-4. The ability of IL-3 to induce expression o
f CD1 molecules and to directly stimulate CD4(-)CD8(-) alpha beta(+) T
CR T lymphocytes raises interest in the role of this cytokine in the d
evelopment, differentiation and function of this T cell subset. (C) 19
96 Academic Press Limited