Induction of Th1-biased cytokine production by alpha-carba-GalCer, a neoglycolipid ligand for NKT cells

Int Immunol. 2010 Apr;22(4):319-28. doi: 10.1093/intimm/dxq012. Epub 2010 Feb 24.

Abstract

NKT cells are characterized by their production of both T(h)1 and T(h)2 cytokines immediately after stimulation with alpha-galactosylceramide (alpha-GalCer), which is composed of alpha-galactopyranose linked to ceramide (itself composed of sphingosine and fatty-acyl chains); the chain length of the ceramide varies and this affects the ability of alpha-GalCer to stimulate cytokine production. However, the contribution of its galactopyranose sugar moiety remains unclear. We synthesized alpha-carba-GalCer, which has an alpha-linked carba-galactosyl moiety; here, the 5a'-oxygen atom of the D-galactopyranose ring of alpha-GalCer is replaced by a methylene group. The alpha-carba-GalCer was more stable and showed higher affinity to the NKT receptor. It thus enhanced and prolonged production of IL-12 and IFN-gamma compared with alpha-GalCer, resulting in augmented NKT cell-mediated adjuvant effects in vivo. The alpha-carba-GalCer, which has an ether linkage, was more resistant to degradation by liver microsomes than was alpha-GalCer, which has an acetal bond. Modulation of the sugar moiety in glycolipids might therefore provide optimal therapeutic reagents for protective immune responses against tumor or pathogens.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Immunologic / chemical synthesis
  • Adjuvants, Immunologic / chemistry
  • Adjuvants, Immunologic / pharmacology*
  • Animals
  • Cell Line
  • Cyclohexanols / chemical synthesis
  • Cyclohexanols / chemistry
  • Cyclohexanols / pharmacology*
  • Cytokines / analysis
  • Cytokines / biosynthesis*
  • Galactosylceramides / chemical synthesis
  • Galactosylceramides / chemistry
  • Galactosylceramides / pharmacology*
  • Glycolipids / metabolism
  • Humans
  • Injections, Intravenous
  • Ligands
  • Mice
  • Natural Killer T-Cells / drug effects*
  • Natural Killer T-Cells / immunology
  • Th1 Cells / immunology*

Substances

  • Adjuvants, Immunologic
  • Cyclohexanols
  • Cytokines
  • Galactosylceramides
  • Glycolipids
  • Ligands