Tracking the response of natural killer T cells to a glycolipid antigen using CD1d tetramers

被引:736
作者
Matsuda, JL
Naidenko, OV
Gapin, L
Nakayama, T
Taniguchi, M
Wang, CR
Koezuka, Y
Kronenberg, M
机构
[1] La Jolla Inst Allergy & Immunol, San Diego, CA 92121 USA
[2] Chiba Univ, Grad Sch Med, CREST, Chiba 2608670, Japan
[3] Chiba Univ, Grad Sch Med, Dept Mol Immunol, Chiba 2608670, Japan
[4] Univ Chicago, Dept Pathol, Gwenn Knapp Ctr Lupus & Immunol Res, Chicago, IL 60637 USA
[5] Kirin Brewery Co Ltd, Pharmaceut Res Lab, Takasaki, Gumma 37012, Japan
关键词
antigen presentation; lipid antigen; T lymphocyte; natural killer cell; tetramer;
D O I
10.1084/jem.192.5.741
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A major group of natural killer (NK) T cells express an invariant V alpha 14(+) T cell receptor (TCR) specific for the lipoglycan alpha-galactosylceramide (alpha-GalCer), which is presented by CD1d. These cells may have an important immune regulatory function, but an understanding of their biology has been hampered by the lack of suitable reagents for tracking them in vivo. Here we show that tetramers of mouse CD1d loaded with alpha-GalCer are a sensitive and highly specific reagent for identifying V alpha 14(+) NK T cells. Using these tetramers, we find that alpha-GalCer-specific T lymphocytes are more widely distributed than was previously appreciated, with populations of largely NK1.1(-) but tetramer-binding T cells present in the lymph nodes and the intestine. Injection of alpha-GalCer leads to the production of both interferon gamma and interleukin 4 by nearly all NK T cells in the liver and the: majority of the spleen within 2 h. These cells mostly disappear by 5 h, and they do not reappear after 1 wk. Curiously, tetramer-positive thymocytes do not rapidly synthesize cytokines, nor do they undergo decreases in cell number after lipid antigen stimulation, although they express equivalent TCR levels. In summary, the data presented here demonstrate chat alpha-GalCer-specific NK T cells undergo a unique and highly compartmentalized response to antigenic stimulation.
引用
收藏
页码:741 / 753
页数:13
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