The main function of dendritic cells (DC) is to induce the differentia
tion of naive T lymphocytes into helper cells producing a large array
of lymphokines, including interleukin (IL)-2; interferon-gamma (IFN-ga
mma), IL-4, IL-5 and IL-10. The potent immunostimulatory properties of
DC develop during a process of maturation that occurs spontaneously i
n vitro. Since IL-10 has been shown to inhibit Th1 responses, we deter
mined its effect on DC maturation and accessory function. Our data sho
w that DC that have undergone maturation in vitro in the presence of I
L-10, have an impaired capacity to induce a Th1-type response in vivo,
leading to the development of Th2 lymphocytes. Their inability to pro
mote the synthesis of IFN-gamma seems to correlate with a decreased pr
oduction of IL-12, an bet erodimeric cytokine necessary for optimal ge
neration of Th1-type cells. These results suggest that IL-10 skews the
Th1/Th2 balance to Th2 in vivo by selectively blocking IL-12 synthesi
s by the antigen-presenting cells that play a role of adjuvant of the
primary immune response. The cytokines present in the environment at t
he presentation step may, therefore, determine the class of the immune
response induced by DC in vivo, i.e. Th0, Th1 and/or Th2.