Abstract |
Invariant NKT (iNKT) cells are innate-like lymphocytes that recognize glycolipid antigens in the context of the MHC class I-like antigen-presenting molecule CD1d. In vivo activation of mouse iNKT cells with the glycolipid alpha-galactosylceramide ( alpha-GalCer) results in the acquisition of a hyporesponsive (anergic) phenotype by these cells. Because iNKT cells can become activated in the context of infectious agents, here we evaluated whether iNKT cell activation by microorganisms can influence subsequent responses of these cells to glycolipid antigen stimulation. We found that mouse iNKT cells activated in vivo by multiple bacterial microorganisms, or by bacterial LPS or flagellin, became unresponsive to subsequent activation with alpha-GalCer. This hyporesponsive phenotype of iNKT cells required IL-12 expression and was associated with changes in the surface phenotype of these cells, reduced severity of concanavalin A-induced hepatitis, and alterations in the therapeutic activities of alpha-GalCer. These findings may have important implications for the development of iNKT cell-based therapies.
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Authors | Sungjune Kim, Saif Lalani, Vrajesh V Parekh, Tiffaney L Vincent, Lan Wu, Luc Van Kaer |
Journal | The Journal of clinical investigation
(J Clin Invest)
Vol. 118
Issue 6
Pg. 2301-15
(Jun 2008)
ISSN: 0021-9738 [Print] United States |
PMID | 18451996
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Galactosylceramides
- Lipopolysaccharides
- alpha-galactosylceramide
- Flagellin
- Interleukin-12
- Interleukin-4
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Topics |
- Animals
- Escherichia coli
(metabolism)
- Flagellin
(metabolism)
- Galactosylceramides
(metabolism)
- Interleukin-12
(metabolism)
- Interleukin-4
(metabolism)
- Killer Cells, Natural
(metabolism, microbiology)
- Kinetics
- Lipopolysaccharides
(metabolism)
- Lymphocytes
(metabolism, microbiology)
- Mice
- Mice, Inbred C57BL
- Models, Biological
- Phenotype
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