Interaction between mannosylated lipoarabinomannan and dendritic cell-specific intercellular adhesion molecule-3 grabbing nonintegrin influences dendritic cells maturation and T cell immunity
► The interaction between manLAM and DC-SIGN was investigated. ► DC-SIGN influenced DCs maturation and downstream immune response. ► Small interfering RNA-expressing lentiviral vectors to specifically knockdown DC-SIGN. ► DC-SIGN knockdown alone in DCs did not affect the maturation or the immunologi...
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Veröffentlicht in: | Cellular immunology 2011, Vol.272 (1), p.94-101 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | ► The interaction between manLAM and DC-SIGN was investigated. ► DC-SIGN influenced DCs maturation and downstream immune response. ► Small interfering RNA-expressing lentiviral vectors to specifically knockdown DC-SIGN. ► DC-SIGN knockdown alone in DCs did not affect the maturation or the immunological function. ► Interaction between manLAM and DC-SIGN affects DCs maturation and downstream T cell immunity.
The aim of the study was to investigate the interaction between manLAM and DC-SIGN influencing DCs maturation and downstream immune response using small interfering RNA-expressing lentiviral vectors to specifically knockdown DC-SIGN. Our data indicated that DC-SIGN knockdown alone in DCs did not affect the maturation or the immunological function of lipopolysacharide (LPS)-activated DCs. Surface molecules were dramatically down-regulated in DCs primed with manLAM but not in mock control DCs (
P
<
0.05). Meanwhile, manLAM enhanced the production of the immunosuppressive cytokine IL-10 in DCs (
P
<
0.05). The level of IFN-γ was significantly down-regulated in the supernatants of naive T cells after co-cultured with DCs primed with manLAM (
P
<
0.05). We demonstrated that DCs primed with manLAM may partially impair maturation phenotypes and immune response in LPS-activated DCs. However, the alterations of DCs function and downstream immune response caused by manLAM were reversed by the knockdown of DC-SIGN. |
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ISSN: | 0008-8749 1090-2163 |
DOI: | 10.1016/j.cellimm.2011.09.001 |