Cutting edge: Hierarchy of chemokine receptor and TCR signals regulating T cell migration and proliferation

被引:139
作者
Bromley, SK
Peterson, DA
Gunn, MD
Dustin, ML
机构
[1] Washington Univ, Sch Med, Dept Pathol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Ctr Immunol, St Louis, MO 63110 USA
[3] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
关键词
D O I
10.4049/jimmunol.165.1.15
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chemokines play an important role in establishing the distribution of lymphocyte subpopulations in primary and secondary lymphoid tissues and in the recruitment of leukocytes to sites of inflammation. However, the potential of chemokines to down-regulate immune responses has not been demonstrated. We now show that certain chemokine gradients have the potential to suppress T cell activation by preventing formation of the immunological synapse, the specialized cell-cell junction that forms before a T cell can be fully activated. Our data reveals an immunosuppressive potential of chemokines engaging the CXCR3 and CCR7 receptors, but not the CXCR4, CCR2, CCR4, or CCR5 receptors, These results suggest a novel mechanism for T cell ignorance of agonist MHC-peptide complexes based on dominant chemokine gradients.
引用
收藏
页码:15 / 19
页数:5
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