Competition for antigen determines the stability of T cell-dendritic cell interactions during clonal expansion

被引:72
作者
Garcia, Zacarias
Pradelli, Emmanuelle
Celli, Susanna
Beuneu, Helene
Simon, Aurelie
Bousso, Philippe [1 ]
机构
[1] Inst Pasteur, Dynam Reponses Immunes G5, F-75015 Paris, France
[2] INSERM, Equipe Avenir, U668, F-75015 Paris, France
关键词
imaging; T cell activation; precursor frequency; two-photon imaging;
D O I
10.1073/pnas.0610019104
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
The regulation of T cell-dendritic cell (DC) contacts during clonal expansion is poorly defined. Although optimal CD4 T cell responses require prolonged exposure to antigen (Ag), it is believed that stable T cell-DC interactions occur only during the first day of the activation process. Here we show that recently activated CD4 T cells are in fact fully competent for establishing contact with Ag-bearing DC. Using two-photon imaging, we found that whereas prolonged interactions between activated T cells and Ag-bearing DCs were infrequentat high T cell precursor frequency, they were readily observed for a period of at least 2 days when lower numbers of T cells were used. We provide evidence that, when present in high numbers, Ag-specific T cells still gained access to the DC surface but were competing for the limited number of sites on DCs with sufficient peptide-MHC complexes for the establishment of a long-lived interaction. Consistent with these findings, we showed that restoration of peptide-MHC level on DCs at late time points was sufficient to recover interactions between activated T cells and DCs. Thus, the period during which CD4 T cells continue to establish stable interactions with DCs is longer than previously thought, and its duration is dictated by both Ag levels and T cell numbers, providing a feedback mechanism for the termination of CD4 T cell responses.
引用
收藏
页码:4553 / 4558
页数:6
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