Reciprocal Control of T Helper Cell and Dendritic Cell Differentiation

Author:

Rissoan Marie-Clotilde1,Soumelis Vassili1,Kadowaki Norimitsu2,Grouard Geraldine1,Briere Francine1,Malefyt René de Waal2,Liu Yong-Jun12

Affiliation:

1. Schering-Plough, Laboratory for Immunological Research, 27 chemin des Peupliers, Boite Postale 11, 69571, Dardilly, France.

2. DNAX Research Institute of Molecular and Cellular Biology, 901 California Avenue, Palo Alto, CA 94304–1104, USA.

Abstract

It is not known whether subsets of dendritic cells provide different cytokine microenvironments that determine the differentiation of either type-1 T helper (T H 1) or T H 2 cells. Human monocyte (pDC1)–derived dendritic cells (DC1) were found to induce T H 1 differentiation, whereas dendritic cells (DC2) derived from CD4 + CD3 CD11c plasmacytoid cells (pDC2) induced T H 2 differentiation by use of a mechanism unaffected by interleukin-4 (IL-4) or IL-12. The T H 2 cytokine IL-4 enhanced DC1 maturation and killed pDC2, an effect potentiated by IL-10 but blocked by CD40 ligand and interferon-γ. Thus, a negative feedback loop from the mature T helper cells may selectively inhibit prolonged T H 1 or T H 2 responses by regulating survival of the appropriate dendritic cell subset.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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