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

Citation
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
Citations number
57
Categorie Soggetti
Immunology
Journal title
JOURNAL OF IMMUNOLOGY
ISSN journal
00221767 → ACNP
Volume
165
Issue
7
Year of publication
2000
Pages
3756 - 3762
Database
ISI
SICI code
0022-1767(20001001)165:7<3756:COMDCS>2.0.ZU;2-M
Abstract
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.