CD1d on myeloid dendritic cells stimulates cytokine secretion from and cytolytic activity of V alpha 24J alpha Q T cells: A feedback mechanism for immune regulation
Oo. Yang et al., CD1d on myeloid dendritic cells stimulates cytokine secretion from and cytolytic activity of V alpha 24J alpha Q T cells: A feedback mechanism for immune regulation, J IMMUNOL, 165(7), 2000, pp. 3756-3762
The precise immunologic functions of CD1d-restricted, CD161(+) AV24AJ18 (V
alpha 24J alpha Q) T cells are not well defined, although production of IL-
4 has been suggested as important for priming Th2 responses, However, activ
ation of human V alpha 224J alpha Q T cell clones by anti-CD3 resulted in t
he secretion of multiple cytokines notably important for the recruitment an
d differentiation of myeloid dendritic cells. Specific activation of V alph
a 24J alpha Q T cells was CD1d restricted. Expression of CD1d was found on
monocyte-derived dendritic cells in vitro, and immunohistochemical staining
directly revealed CD1d preferentially expressed on dendritic cells in the
paracortical T cell zones of lymph nodes. Moreover, myeloid dendritic cells
both activated V alpha 24J alpha Q T cells and were susceptible to lysis b
y these same regulatory T cells. Because myeloid dendritic cells are a majo
r source of IL-12 and control Th1 cell differentiation, their elimination b
y lysis is a mechanism for limiting the generation of Th1 cells and thus re
gulating Th1/Th2 responses.