Identification of C-glycoside analogues that display a potent biological activity against murine and human invariant natural killer T cells

被引:54
作者
Li, Xiangming [1 ]
Chen, Guangwu [2 ]
Garcia-Navarro, Raquel [1 ]
Franck, Richard W. [2 ]
Tsuji, Moriya [1 ]
机构
[1] Rockefeller Univ, Aaron Diamond AIDS Res Ctr, HIV & Malaria Vaccine Program, New York, NY 10016 USA
[2] CUNY Hunter Coll, Dept Chem, New York, NY 10021 USA
关键词
CD1d; C-glycoside; mouse and human iNKT cells; T helper 1-type response; LIGAND ALPHA-GALACTOSYLCERAMIDE; NKT CELLS; DENDRITIC CELLS; PHASE-I; ACTIVATION; RESPONSES; RECEPTOR; RECOGNITION; GLYCOLIPIDS; ADJUVANT;
D O I
10.1111/j.1365-2567.2008.02943.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have recently shown that alpha-C-galactosylceramide (alpha-C-GalCer) stimulates invariant natural killer T (iNKT) cells and preferentially induces a T helper 1 (Th1)-type response in mice. However, alpha-C-GalCer was found to be a rather weak ligand against human iNKT cells in vitro. Therefore, in this study, we sought to identify a compound that displays a strong stimulatory activity against human iNKT cells, by determining the biological activities of several C-glycoside analogues. From the in vitro screening assays, we found that almost all C-glycoside analogues, which have an E-alkene linker between sugar and lipid moieties, are able to activate human iNKT cells and to induce the maturation and activation of human dendritic cells through iNKT-cell activation. In summary, although alpha-galactosylceramide (alpha-GalCer) remains the strongest iNKT-cell ligand, our study identified E-alkene-linked C-glycoside analogues as potent human iNKT-cell stimulants, and indicated that these analogues could be used as a therapeutic agent in the future for diseases resolved by Th1-type responses.
引用
收藏
页码:216 / 225
页数:10
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