Bacterial glycolipids and analogs as antigens for CD1d-restricted NKT cells

被引:198
作者
Wu, D
Xing, GW
Poles, MA
Horowitz, A
Kinjo, Y
Sullivan, B
Bodmer-Narkevitch, V
Plettenburg, O
Kronenberg, M
Tsuji, M
Ho, DD
Wong, CH
机构
[1] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[3] Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10016 USA
[4] NYU, Sch Med, Dept Med & Mol Parasitol, New York, NY 10010 USA
[5] NYU, Sch Med, Dept Med, Div Gastroenterol, New York, NY 10010 USA
[6] La Jolla Inst Allergy & Immunol, Div Dev Immunol, San Diego, CA 92121 USA
关键词
D O I
10.1073/pnas.0408696102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The CD1 family of proteins binds self and foreign glycolipids for presentation to CD1-restricted T cells. To identify previously uncharacterized active CD1 ligands, especially those of microbial origin, numerous glycolipids were synthesized and tested for their ability to stimulate mouse and human natural killer T (NKT) cells. They included analogs of the well known NKT cell agonist alpha-galactosyl ceramide (alpha-GalCer), bacterial glycolipids, and variations of the self-glycolipid, sulfatide. Bacterial glycolipids, alpha-galacturonosyl-ceramides from Sphingomonas wittichii, although structurally similar to alpha-GalCer, have significant differences in the sugar head group as well as the ceramide portion. The Sphingomonas glycosphingolipids (GSLs) and sulfatide variants were shown to activate human NKT cells as measured by IL-4 and IFN-gamma secretion. Moreover, CD1d-dimer staining revealed human NKT cell reactivity toward these GSLs and to the sulfatides in a fashion comparable with alpha-GalCer. Because alpha-GalCer is a marine-sponge-derived ligand, our study here shows that bacterium-derived antigens are also able to stimulate mouse and human NKT cells.
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页码:1351 / 1356
页数:6
相关论文
共 32 条
[1]   The crystal structure of human CD1b with a bound bacterial glycolipid [J].
Batuwangala, T ;
Shepherd, D ;
Gadola, SD ;
Gibson, KJC ;
Zaccai, NR ;
Fersht, AR ;
Besra, GS ;
Cerundolo, V ;
Jones, EY .
JOURNAL OF IMMUNOLOGY, 2004, 172 (04) :2382-2388
[2]   A newly discovered cholesteryl galactoside from Borrelia burgdorferi [J].
Ben-Menachem, G ;
Kubler-Kielb, J ;
Coxon, B ;
Yergey, A ;
Schneerson, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (13) :7913-7918
[3]   CD1d-mediated recognition of an α-galactosylceramide by natural killer T cells is highly conserved through mammalian evolution [J].
Brossay, L ;
Chioda, M ;
Burdin, N ;
Koezuka, Y ;
Casorati, G ;
Dellabona, P ;
Kronenberg, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (08) :1521-1528
[4]  
Brossay L, 1998, J IMMUNOL, V161, P5124
[5]  
Burdin N, 1999, EUR J IMMUNOL, V29, P2014, DOI 10.1002/(SICI)1521-4141(199906)29:06<2014::AID-IMMU2014>3.0.CO
[6]  
2-G
[7]   2 CLASSES OF CD1 GENES [J].
CALABI, F ;
JARVIS, JM ;
MARTIN, L ;
MILSTEIN, C .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1989, 19 (02) :285-292
[8]   Highly efficient glycosylation of sapogenins [J].
Deng, SJ ;
Yu, B ;
Xie, JM ;
Hui, YZ .
JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (19) :7265-7266
[9]   The adaptor protein AP-3 is required for CD1d-mediated antigen presentation of glycosphingolipids and development of Vα14i NKT cells [J].
Elewaut, D ;
Lawton, AP ;
Nagarajan, NA ;
Maverakis, E ;
Khurana, A ;
Höning, S ;
Benedict, CA ;
Sercarz, E ;
Bakke, O ;
Kronenberg, M ;
Prigozy, TI .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (08) :1133-1146
[10]   Mycobacterial phosphatidylinositol mannoside is a natural antigen for old-restricted T cells [J].
Fischer, K ;
Scotet, E ;
Niemeyer, M ;
Koebernick, H ;
Zerrahn, J ;
Maillet, S ;
Hurwitz, R ;
Kursar, M ;
Bonneville, M ;
Kaufmann, SHE ;
Schaible, UE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (29) :10685-10690