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Biomedical and Environmental Sciences ; (12): 350-356, 2010.
Article Dans Anglais | WPRIM | ID: wpr-306918

Résumé

<p><b>OBJECTIVE</b>To explore the immune stimulation effect of recombinant E.coli LLO/OVA on mice bone marrow-derived dendritic cells (BMDCs) and T lymphocytes in vitro.</p><p><b>METHODS</b>After BMDCs stimulated by E.coli LLO/OVA, their Toll-like receptor (TLR) and nucleotide-binding oligomerization domain (NOD) receptor signalling pathway were examined by superarray hybridization; and the priming effect of the vaccine activated BMDCs on CD4(+)T and CD8(+)T was determined by [3H]thymidine uptake and ELISA, the tumor cytotoxic effect of activated CD8(+)T cells was determined by cytotoxic assay.</p><p><b>RESULTS</b>After BMDCs were activated by E. coli LLO/OVA via TLR4, NOD1 receptor and NF-κB signalling pathway, the expression of their surface molecules including MHC class I, MHC class II, CD40, CD80 and CD86 significantly up-regulated; the secretion of IL-12 and IFN-γ increased also. The mature BMDCs stimulated the allergic CD4(+)T and CD8(+)T cells proliferation and their IL-2 and IFN-γ secretion, and the activated CD8(+)T cells effectively killed B16-OVA melanoma cells and RMA-S/OVA lymphoma cells in vitro.</p><p><b>CONCLUSION</b>E.coli LLO/OVA is effective in inducing BMDCs maturation via activating TLR4 and NOD1 receptor signalling pathway and promoting specific anti-tumor T cell immunity in vitro.</p>


Sujets)
Animaux , Femelle , Souris , Antigènes néoplasiques , Génétique , Pharmacologie , Toxines bactériennes , Génétique , Pharmacologie , Vaccins anticancéreux , Génétique , Pharmacologie , Lignée cellulaire tumorale , Prolifération cellulaire , Survie cellulaire , Allergie et immunologie , Techniques de coculture , Cytokines , Allergie et immunologie , Sécrétions corporelles , Cellules dendritiques , Biologie cellulaire , Allergie et immunologie , Métabolisme , Test ELISA , Escherichia coli , Génétique , Métabolisme , Cytométrie en flux , Protéines du choc thermique , Génétique , Pharmacologie , Hémolysines , Génétique , Pharmacologie , Immunité innée , Souris de lignée C57BL , Protéine adaptatrice de signalisation NOD1 , Génétique , Physiologie , Ovalbumine , Génétique , Pharmacologie , Protéines de fusion recombinantes , Génétique , Pharmacologie , RT-PCR , Lymphocytes T cytotoxiques , Allergie et immunologie , Récepteur de type Toll-4 , Génétique , Physiologie
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