Glycolipid antigen processing for presentation by CD1d molecules

被引:251
|
作者
Prigozy, TI
Naidenko, O
Qasba, P
Elewaut, D
Brossay, L
Khurana, A
Natori, T
Koezuka, Y
Kulkarni, A
Kronenberg, M
机构
[1] La Jolla Inst Allergy & Immunol, Div Dev Immunol, San Diego, CA 92121 USA
[2] NINCDS, Dev & Metab Neurol Branch, NIH, Bethesda, MD 20892 USA
[3] Kirin Brewery Co Ltd, Pharmaceut Res Lab, Gunma 37012, Japan
[4] Natl Inst Dent & Craniofacial Res, Funct Genom Unit, Bethesda, MD 20892 USA
关键词
D O I
10.1126/science.291.5504.664
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 requirement for processing glycolipid antigens in T cell recognition was examined with mouse CD1d-mediated responses to glycosphingolipids (GSLs). Although some disaccharide GSL antigens can be recognized without processing, the responses to three other antigens, including the disaccharide GSL Gal(alpha1-->2)GalCer (Gal, galactose; GalCer, galactosylceramide), required removal of the terminal sugars to permit interaction with the T cell receptor. A Lysosomal enzyme, alpha -galactosidase A, was responsible for the processing of Gal(alpha1-->2)GalCer to generate the antigenic monosaccharide epitope. These data demonstrate a carbohydrate antigen processing system analogous to that used for peptides and an ability of T cells to recognize processed fragments of complex glycolipids.
引用
收藏
页码:664 / 667
页数:4
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