| Literature DB >> 18981145 |
Emmanuelle Henry1, Christophe J Desmet, Virginie Garzé, Laurence Fiévez, Denis Bedoret, Carlo Heirman, Pedro Faisca, Fabrice J Jaspar, Philippe Gosset, Alain P A Jacquet, Daniel Desmecht, Kris Thielemans, Pierre Lekeux, Muriel Moser, Fabrice Bureau.
Abstract
Dendritic cells (DCs) are professional APCs that have a unique capacity to initiate primary immune responses, including tolerogenic responses. We have genetically engineered bone marrow-derived DCs to express the immunosuppressive cytokine IL-10 and tested the ability of these cells to control experimental asthma. A single intratracheal injection of OVA-pulsed IL-10-transduced DCs (OVA-IL-10-DCs) to naive mice before OVA sensitization and challenge prevented all of the cardinal features of airway allergy, namely, eosinophilic airway inflammation, airway hyperreactivity, and production of mucus, Ag-specific Igs, and IL-4. OVA-IL-10-DCs also reversed established experimental asthma and had long-lasting and Ag-specific effects. We furthermore showed, by using IL-10-deficient mice, that host IL-10 is required for mediating the immunomodulatory effects of OVA-IL-10-DCs and demonstrated a significant increase in the percentage of OVA-specific CD4(+)CD25(+)Foxp3(+)IL-10(+) regulatory T cells in the mediastinal lymph nodes of OVA-IL-10-DC-injected mice. Finally, adoptive transfer of CD4(+) mediastinal lymph node T cells from mice injected with OVA-IL-10-DCs protected OVA-sensitized recipients from airway eosinophilia upon OVA provocation. Our study describes a promising strategy to induce long-lasting Ag-specific tolerance in airway allergy.Entities:
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Year: 2008 PMID: 18981145 DOI: 10.4049/jimmunol.181.10.7230
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422