Journal of Leukocyte Biology
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Originally published online as doi:10.1189/jlb.0704383 on August 4, 2005

Published online before print August 4, 2005
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(Journal of Leukocyte Biology. 2005;78:954-966.)
© 2005 by Society for Leukocyte Biology

Virus overrides the propensity of human CD40L-activated plasmacytoid dendritic cells to produce Th2 mediators through synergistic induction of IFN-{gamma} and Th1 chemokine production

Nathalie Bendriss-Vermare*,{dagger},1, Stéphanie Burg*, Holger Kanzler{ddagger},3, Laurence Chaperot§, Thomas Duhen*, Odette de Bouteiller*, Marjorie D’agostini*, Jean-Michel Bridon*, Isabelle Durand*, Joel M. Sederstrom||, Wei Chen||, Joël Plumas§, Marie-Christine Jacob§, Yong-Jun Liu{ddagger},4, Pierre Garrone*, Giorgio Trinchieri*, Christophe Caux*,2 and Francine Brière*

* Laboratory for Immunological Research, Schering-Plough Research Institute, Dardilly, France;
{dagger} INSERM U590, Centre Léon Bérard, Lyon, France;
{ddagger} DNAX Research Institute of Molecular and Cellular Biology, Palo Alto, California;
§ Department of Research and Development, Research Group on Lymphoma, EFS Rhône-Alpes Grenoble, La Tronche, France; and
|| University of Minnesota Cancer Center, Minneapolis, Minnesota

1Correspondence: INSERM U590, Centre Léon Bérard, Lyon, France. E-mail: bendris{at}lyon.fnclcc.fr

Depending on the activation status, plasmacytoid dendritic cells (PDC) and myeloid DC have the ability to induce CD4 T cell development toward T helper cell type 1 (Th1) or Th2 pathways. Thus, we tested whether different activation signals could also have an impact on the profile of chemokines produced by human PDC. Signals that induce human PDC to promote a type 1 response (i.e., viruses) and a type 2 response [i.e., CD40 ligand (CD40L)] also induced PDC isolated from tonsils to secrete chemokines preferentially attracting Th1 cells [such as interferon-{gamma} (IFN-{gamma})-inducible protein (IP)-10/CXC chemokine ligand 10 (CXCL10) and macrophage inflammatory protein-1ß/CC chemokine ligand 4 (CCL4)] or Th2 cells (such as thymus and activation-regulated chemokine/CCL17 and monocyte-derived chemokine/CCL22), respectively. Activated natural killer cells were preferentially recruited by supernatants of virus-activated PDC, and supernatants of CD40L-activated PDC attracted memory CD4+ T cells, particularly the CD4+CD45RO+CD25+ T cells described for their regulatory activities. It is striking that CD40L and virus synergized to trigger the production of IFN-{gamma} by PDC, which induces another Th1-attracting chemokine monokine-induced by IFN-{gamma}/CXCL9 and cooperates with endogenous type I IFN for IP-10/CXCL10 production. In conclusion, our studies reveal that PDC participate in the selective recruitment of effector cells of innate and adaptive immune responses and that virus converts the CD40L-induced Th2 chemokine patterns of PDC into a potent Th1 mediator profile through an autocrine loop of IFN-{gamma}.

Key Words: PDC • migration • memory T cells • NK cells • chemokines




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