Dynamic imaging of chemokine-dependent CD8+ T cell help for CD8+ T cell responses

被引:107
作者
Hugues, Stephanie [1 ]
Scholer, Alix
Boissonnas, Alexandre
Nussbaum, Alexander
Combadiere, Christophe
Amigorena, Sebastian
Fetler, Luc
机构
[1] Ctr Rech, Inst Curie, F-75248 Paris, France
[2] Inst Curie, U653, Inst Natl Sante & Rech Med, F-75248 Paris, France
[3] Hop La Pitie Salpetriere, Lab Immunol Cellulaire, U543, Inst Natl Sante & Rech Med, F-75013 Paris, France
[4] Inst Curie, Lab Physicochim Curie, UMR 168, CNRS, F-75248 Paris, France
关键词
D O I
10.1038/ni1495
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Naive T lymphocytes move efficiently in lymphoid tissues while scanning dendritic cells in search of cognate complexes of peptide in major histocompatibility molecules. However, T cell migration ceases after recognition of cognate antigen. We show here that during the initiation of antigen-specific CD8(+) T cell responses, naive CD8(+) polyclonal T cells 'preferentially' interacted in an antigen-independent way with mature dendritic cells competent to present antigen to antigen-specific CD8(+) T cells. These antigen-independent interactions required expression of the chemokine receptor CCR5 on polyclonal T cells and increased the efficiency of the induction of naive, low-precursor-frequency CD8(+) T cell responses. Thus, antigen-specific CD8(+) T cells favor the priming of naive CD8(+) T cells by promoting the CCR5-dependent recruitment of polyclonal CD8(+) T cells to mature dendritic cells.
引用
收藏
页码:921 / 930
页数:10
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