ICOS costimulates invariant NKT cell activation

被引:40
作者
Kaneda, H
Takeda, K [1 ]
Ota, T
Kaduka, Y
Akiba, H
Ikarashi, Y
Wakasugi, H
Kronenberg, M
Kinoshita, K
Yagita, H
Okumura, K
机构
[1] Juntendo Univ, Sch Med, Dept Immunol, Tokyo 1138421, Japan
[2] Juntendo Univ, Sch Med, Dept Obstet & Ginecol, Tokyo 1138421, Japan
[3] Natl Canc Ctr, Div Pharmacol, Tokyo 1040045, Japan
[4] La Jolla Inst Allergy & Immunol, Div Dev Immunol, San Diego, CA 92121 USA
基金
美国国家卫生研究院;
关键词
NKT cells; alpha-galactosylceramide; ICOS; CD28; IFN-gamma; IL-4; cytotoxicity; anti-tumor effect;
D O I
10.1016/j.bbrc.2004.12.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It has been reported that costimulatory molecules, CD80/86-CD28 and CD154-CD40, critically contribute to activation of CD1d-restricted invariant NKT (iNKT) cells. Here we have demonstrated that ICOS, a new member of the CD28 family, plays a substantial role in iNKT cell activation. iNKT cells constitutively expressed ICOS as well as CD28 independently, and ICOS expression was further up-regulated 2-3 days after alpha-galactosylceramide (alpha-GalCer) treatment. Blockade of ICOS-mediated costimulation by administration of anti-ICOS ligand (B7RP-1) mAb or by ICOS gene knockout substantially inhibited alpha-GalCer-induced IFN-gamma and IL-4 production, cytotoxic activity, and anti-metastatic effect. Moreover, blockade of both B7RP-1-ICOS and CD80/86-CD28 interactions mostly abolished the alpha-GalCer-induced immune responses. These findings indicate that iNKT cell activation is regulated by CD28 and IOCS independently. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:201 / 207
页数:7
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