Cutting edge: A critical role for CD70 in CD8 T cell priming by CD40-licensed APCs

被引:106
作者
Taraban, VY [1 ]
Rowley, TF [1 ]
Al-Shamkhani, A [1 ]
机构
[1] Univ Southampton, Southampton Gen Hosp, Sch Med, Tenovus Res Lab,Canc Sci Div, Southampton SO16 6YD, Hants, England
关键词
D O I
10.4049/jimmunol.173.11.6542
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 CD154/CD40 interaction is an important pathway of CD4 T cell help for CD8 T cell responses. In this study, we address the role of CD70, a member of the TNFsuperfamily and the ligand for the T cell costimulatory receptor CD27, in CD40-mediated priming of CD8 T cells. Using an agonistic anti-CD40 mAb to mimic the CD154/CD40 interaction we demonstrate that the priming of OT-I TCR transgenic or endogenous mouse OVA-specific CD8 T cells is critically dependent on CD70/CD27 interaction. CD70 blockade inhibited CD40-mediated clonal expansion of CD8 T cells and reduced the number of memory CD8 T cells generated. Furthermore, CD70 blockade during the initial priming of CD8 T cells inhibited the ability of memory CD8 T cells to expand in response to a second encounter with Ag. Our data indicate that CD70 expression on APCs plays a key role in CD40-dependent CD8 T cell responses.
引用
收藏
页码:6542 / 6546
页数:5
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