B7-H1 (PD-L1) on T cells is required for T-cell-mediated conditioning of dendritic cell maturation

被引:60
作者
Talay, Oezcan [1 ,2 ]
Shen, Ching-Hung [1 ,2 ]
Chen, Lieping [3 ]
Chen, Jianzhu [1 ,2 ]
机构
[1] MIT, Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
[3] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21231 USA
基金
美国国家卫生研究院;
关键词
DC conditioning; DC matuation; T cell activation; IN-VIVO; DEPENDENT MATURATION; IMMUNE-RESPONSE; B7; FAMILY; INFECTION; RECOGNITION; EXPRESSION; ACTIVATION; SYSTEM; LIVER;
D O I
10.1073/pnas.0813367106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Studies have shown that T-cell-dendritic cell (DC) interaction is required for efficient DC maturation. However, the identities of the molecules that mediate the interaction in vivo are largely unknown. Here, we show that maturation of DCs as well as CD8 T-cell responses were impaired in B7-H1-deficient (B7-H1(-/-)) mice to influenza virus infection. Both defects were restored by transferring B7-H1-expressing naive T cells into B7-H1(-/-) mice. Similarly, transferring DCs from wild-type mice or from RAG1(-/-) mice that had been injected with B7-H1-expressing naive T cells also restored CD8 T-cell responses in B7-H1(-/-) mice. These results demonstrate that B7-H1 on naive T cells is required to condition immature DCs to undergo efficient maturation when they encounter microbial infection. In return, the mature DCs stimulate a robust T-cell reponse against the infecting pathogen.
引用
收藏
页码:2741 / 2746
页数:6
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