| Literature DB >> 21493160 |
Andrew E Hogan1, Vincent O'Reilly, Margaret R Dunne, Ravindra T Dere, Shijuan G Zeng, Cashel O'Brien, Sylvie Amu, Padraic G Fallon, Mark A Exley, Cliona O'Farrelly, Xiangming Zhu, Derek G Doherty.
Abstract
Activation of CD1d-restricted invariant NKT (iNKT) cells with the glycolipid α-galactosylceramide (α-GalCer) confers protection against disease in murine models, however, clinical trials in humans have had limited impact. We synthesized a novel thioglycoside analogue of α-GalCer, denoted α-S-GalCer, and tested its efficacy for stimulating human iNKT cells in vitro. α-S-GalCer stimulated cytokine release by iNKT cells in a CD1d-dependent manner and primed CD1d(+) target cells for lysis. α-S-GalCer-stimulated iNKT cells induced maturation of monocyte-derived dendritic cells into antigen-presenting cells that released IL-12 and small amounts of IL-10. The nature and potency of α-S-GalCer and α-GalCer in human iNKT cell activation were similar. However, in contrast to α-GalCer, α-S-GalCer did not activate murine iNKT cells in vivo. Because of its enhanced stability in biological systems, α-S-GalCer may be superior to α-GalCer as a parent compound for developing adjuvant therapies for humans.Entities:
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Year: 2011 PMID: 21493160 DOI: 10.1016/j.clim.2011.03.016
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969