Ox40-ligand has a critical costimulatory role in dendritic cell: T cell interactions

被引:258
作者
Chen, AI
McAdam, AJ
Buhlmann, JE
Scott, S
Lupher, ML
Greenfield, EA
Baum, PR
Fanslow, WC
Calderhead, DM
Freeman, GJ
Sharpe, AH
机构
[1] Brigham & Womens Hosp, Dept Pathol, Div Immunol Res, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Adult Oncol, Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[5] Immunex Res & Dev Corp, Seattle, WA 98101 USA
[6] Dartmouth Med Sch, Lebanon, NH 03756 USA
关键词
D O I
10.1016/S1074-7613(00)80143-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The tumor necrosis factor family molecule Ox40-ligand (Ox40L) has been identified as a potential costimulatory molecule and also has been implicated in T cell homing and B cell activation. To ascertain the essential functions of Ox40L, we generated and characterized Ox40L-deficient mice. Mice lacking Ox40L exhibit an impaired contact hypersensitivity response, a dendritic cell-dependent T cell-mediated response, due to defects in T cell priming and cytokine production. In contrast, Ox40L-deficient mice do not have defects in T cell homing or humoral immune responses. In vitro, Ox40L-deficient dendritic cells are defective in costimulating T cell cytokine production. Thus, Ox40L has a critical costimulatory function in vitro and in vivo for dendritic cell:T cell interactions.
引用
收藏
页码:689 / 698
页数:10
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