Reciprocal Control of T Helper Cell and Dendritic Cell Differentiation

Marie‐Clotilde Rissoan(Materials Design (France)), Vassili Soumelis(Materials Design (France)), Norimitsu Kadowaki(Cellular Research (United States)), Géraldine Grouard(Materials Design (France)), Francine Brière(Materials Design (France)), René de Waal Malefyt(Cellular Research (United States)), Yong-Jun Liu(Materials Design (France))
Science
February 19, 1999
Cited by 1,853

Abstract

It is not known whether subsets of dendritic cells provide different cytokine microenvironments that determine the differentiation of either type-1 T helper (TH1) or TH2 cells. Human monocyte (pDC1)-derived dendritic cells (DC1) were found to induce TH1 differentiation, whereas dendritic cells (DC2) derived from CD4+CD3-CD11c- plasmacytoid cells (pDC2) induced TH2 differentiation by use of a mechanism unaffected by interleukin-4 (IL-4) or IL-12. The TH2 cytokine IL-4 enhanced DC1 maturation and killed pDC2, an effect potentiated by IL-10 but blocked by CD40 ligand and interferon-gamma. Thus, a negative feedback loop from the mature T helper cells may selectively inhibit prolonged TH1 or TH2 responses by regulating survival of the appropriate dendritic cell subset.


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