Skip Navigation



International Immunology Advance Access published online on March 29, 2004

International Immunology, doi:10.1093/intimm/dxh077
© 2004 by The Japanese Society for Immunology
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
16/5/767    most recent
dxh077v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Rouas, R.
Right arrow Articles by Martiat, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rouas, R.
Right arrow Articles by Martiat, P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Received January 14, 2004
Accepted February 23, 2004

Article

Poly(I:C) used for human dendritic cell maturation preserves their ability to secondarily secrete bioactive IL-12

Redouane Rouas 1, Philippe Lewalle 1, Frank El Ouriaghli 1, Berengere Nowak 1, Hughes Duvillier 1, Philippe Martiat 1*

1 Laboratory of Experimental Hematology, Jules Bordet Institute, Free University of Brussels, 1000 Brussels, Belgium

* To whom correspondence should be addressed. E-mail: pmartiat{at}ulb.ac.be.


   Abstract

Dendritic cells (DC) are professional antigen-presenting cells that play a central role in the control of immunity. Mature DC are characterized by high expression levels of MHC and co-stimulatory molecules, and by the secretion of IL-12, a key cytokine for the priming of cytotoxic T lymphocytes. Here, we have compared different maturation stimuli to reproducibly generate stable mature DC secreting high amounts of bioactive IL-12p70. We have compared soluble human trimeric CD40 ligand (sCD40L) combined with IFN-{gamma}, poly(I:C), a cocktail of cytokines (IL-1{beta}, IL-6 and tumor necrosis factor-{alpha}) with prostaglandin E2 and lipopolysaccharide. A major concern, however, is whether DC, that have already produced high amounts of IL-12p70 during the maturation step, are still capable of secreting IL-12p70 after in vivo administration at the time of interaction with the targeted T cells. To mimic that situation, mature DC generated by those methods were compared for their ability to secrete IL-12p70 in the absence of IFN-{gamma}, using sCD40L. We observed a second consistent secretion of bioactive IL-12p70 upon subsequent sCD40L stimulation only when poly(I:C) was used as the maturating agent. Our data suggest that, for clinical use, poly(I:C) may be one of the most appropriate agents to generate stable mature DC. These mature DC might generate in vivo effective immune responses after injection, because they retain the ability to secrete bioactive IL-12 after CD40 ligation.

Keywords: Keywords: CD40 ligand, IL-12, immunotherapy, mature dendritic cell


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Leukoc. Biol.Home page
X.-L. Huang, Z. Fan, L. Borowski, and C. R. Rinaldo
Maturation of dendritic cells for enhanced activation of anti-HIV-1 CD8+ T cell immunity
J. Leukoc. Biol., June 1, 2008; 83(6): 1530 - 1540.
[Abstract] [Full Text] [PDF]


Home page
J. Leukoc. Biol.Home page
K. Breckpot, J. Corthals, A. Bonehill, A. Michiels, S. Tuyaerts, C. Aerts, C. Heirman, and K. Thielemans
Dendritic cells differentiated in the presence of IFN-{beta} and IL-3 are potent inducers of an antigen-specific CD8+ T cell response
J. Leukoc. Biol., October 1, 2005; 78(4): 898 - 908.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.