Cooperative B7-1/2 (CD80/CD86) and B7-DC costimulation of CD4+ T cells independent of the PD-1 receptor

被引:135
作者
Shin, T
Kennedy, G
Gorski, K
Tsuchiya, H
Koseki, H
Azuma, M
Yagita, H
Chen, LP
Powell, J
Pardoll, D
Housseau, F
机构
[1] Johns Hopkins Univ, Sch Med, Sidney Kiddel COmprehens Canc Ctr, Baltimore, MD 21231 USA
[2] Chiba Univ, Dept Mol Embryol, Chuo Ku, Chiba 2608670, Japan
[3] RIKEN, Res Ctr Allergy & Immunol, Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[4] Tokyo Med & Dent Univ, Dept Immunobiol, Tokyo 1138549, Japan
[5] Juntendo Univ, Sch Med, Dept Immunol, Tokyo 1138429, Japan
[6] Mayo Clin & Mayo Fdn, Dept Immunol, Rochester, MN 55905 USA
关键词
B7; CD40L; costimulatory molecule; PD-1; T cell activation;
D O I
10.1084/jem.20030242
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
B7-DC is a recently discovered member of the 137 family that binds to PD-1 and is selectively expressed by dendritic cells (DCs). It has been shown to either costimulate or inhibit T cell responses. To assess the role of B7-DC in DC-T cell interactions, DCs from B7-DC knockout (KO) mice were generated and compared with DCs from wild-type (WT) and B7-1/B7-2 double KO mice. B7-1/B7-2-deficient DCs, while strongly diminished in their ability to stimulate naive CD4(+) T cells, nonetheless retain partial activity. DCs from B7-DC KO mice are diminished in their ability to activate CD4(+) T cells, demonstrating that DC-expressed B7-DC serves a predominantly stimulatory rather than inhibitory function in the initiation of T cell responses. B7-DC costimulates expression of CD40L with faster kinetics than B7-1 and displays potent synergy with B7-1 and B7-2 for T cell proliferation and cytokine production, indicating that these 137 family members work in concert to stimulate T cells. Finally, costimulation with B7-DC alone or in con unction with B7-1 is PD-1 independent, indicating that B7-DC costimulates T cells via a second receptor.
引用
收藏
页码:31 / 38
页数:8
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