Cutting edge:: Analysis of human Vα24+CD8+ NK T cells activated by α-galactosylceramide-pulsed monocyte-derived dendritic cells

被引:109
作者
Takahashi, T
Chiba, S
Nieda, M
Azuma, T
Ishihara, S
Shibata, Y
Juji, T
Hirai, H
机构
[1] Univ Tokyo, Grad Sch Med, Dept Hematol & Oncol, Tokyo, Japan
[2] Univ Tokyo, Grad Sch Med, Dept Transfus Med, Tokyo, Japan
[3] Univ Tokyo, Grad Sch Med, Dept Urol, Tokyo, Japan
[4] Univ Tokyo, Grad Sch Med, Dept Surg, Tokyo, Japan
[5] Japanese Red Cent Blood Ctr, Res Dept, Tokyo, Japan
关键词
D O I
10.4049/jimmunol.168.7.3140
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human Valpha24(+) NKT cells constitute a counterpart of mouse Valpha14(+) NKT cells, both of which use an invariant TCR-alpha chain. The human Valpha24(+) NKT cells as well as mouse Valpha14(+) NKT cells are activated by glycolipids in a CD1d-restricted manner and produce many immunomodulatory cytokines, possibly affecting the immune balance. In mice, it has been considered from extensive investigations that Valpha14(+) CD8(+) NKT cells that express invariant TCR do not exist. Here we introduce human Valpha24(+)CD8(+) NKT cells. These cells share important features of Valpha24(+) NKT cells in common, but in contrast to CD4(-)CD8(-) (double-negative) or CD4(+) Valpha24(+) NKT cells, they do not produce IL-4. Our discovery may extend and deepen the research field of Valpha24(+) NKT cells as well as help to understand the mechanism of the immune balance-related diseases.
引用
收藏
页码:3140 / 3144
页数:5
相关论文
共 30 条
[1]   MOUSE NK1(+) T-CELLS [J].
BENDELAC, A .
CURRENT OPINION IN IMMUNOLOGY, 1995, 7 (03) :367-374
[2]   Mouse CD1-specific NK1 T cells: Development, specificity, and function [J].
Bendelac, A ;
Rivera, MN ;
Park, SH ;
Roark, JH .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :535-562
[3]   A SUBSET OF CD4(+) THYMOCYTES SELECTED BY MHC CLASS-I MOLECULES [J].
BENDELAC, A ;
KILLEEN, N ;
LITTMAN, DR ;
SCHWARTZ, RH .
SCIENCE, 1994, 263 (5154) :1774-1778
[4]   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
[5]   DEVELOPMENTALLY REGULATED EXPRESSION OF T-CELL RECEPTOR BETA-CHAIN VARIABLE DOMAINS IN IMMATURE THYMOCYTES [J].
BUDD, RC ;
MIESCHER, GC ;
HOWE, RC ;
LEES, RK ;
BRON, C ;
MACDONALD, HR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1987, 166 (02) :577-582
[6]  
Chen HJ, 1997, J IMMUNOL, V159, P2240
[7]   Requirement for V(alpha)14 NKT cells in IL-12-mediated rejection of tumors [J].
Cui, JQ ;
Shin, T ;
Kawano, T ;
Sato, H ;
Kondo, E ;
Toura, I ;
Kaneko, Y ;
Koseki, H ;
Kanno, M ;
Taniguchi, M .
SCIENCE, 1997, 278 (5343) :1623-1626
[8]  
Davodeau F, 1997, J IMMUNOL, V158, P5603
[9]   AN INVARIANT V-ALPHA-24-J-ALPHA-Q/V-BETA-11 T-CELL RECEPTOR IS EXPRESSED IN ALL INDIVIDUALS BY CLONALLY EXPANDED CD4-8- T-CELLS [J].
DELLABONA, P ;
PADOVAN, E ;
CASORATI, G ;
BROCKHAUS, M ;
LANZAVECCHIA, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (03) :1171-1176
[10]  
Emoto M, 2000, EUR J IMMUNOL, V30, P2300, DOI 10.1002/1521-4141(2000)30:8<2300::AID-IMMU2300>3.0.CO