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
相关论文
共 32 条
[1]  
Alcover A, 2000, CRIT REV IMMUNOL, V20, P325
[2]   Regulating T helper cell immunity through antigen responsiveness and calcium entry [J].
Bikah, G ;
Pogue-Caley, RR ;
McHeyzer-Williams, LJ ;
McHeyzer-Williams, MG .
NATURE IMMUNOLOGY, 2000, 1 (05) :402-412
[3]   Dynamics of CD8+ T cell priming by dendritic cells in intact lymph nodes [J].
Bousso, P ;
Robey, E .
NATURE IMMUNOLOGY, 2003, 4 (06) :579-585
[4]   Cellular orchestration of T cell priming in lymph nodes [J].
Breart, Beatrice ;
Bousso, Philippe .
CURRENT OPINION IN IMMUNOLOGY, 2006, 18 (04) :483-490
[5]   CD4+ T cells that enter the draining lymph nodes after antigen injection participate in the primary response and become central-memory cells [J].
Catron, DM ;
Rusch, LK ;
Hataye, J ;
Itano, AA ;
Jenkins, MK .
JOURNAL OF EXPERIMENTAL MEDICINE, 2006, 203 (04) :1045-1054
[6]   CD4 T cells integrate signals delivered during successive DC encounters in vivo [J].
Celli, S ;
Garcia, Z ;
Bousso, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (09) :1271-1278
[7]   Cutting edge:: T lymphocyte activation by repeated immunological synapse formation and intermittent signaling [J].
Faroudi, M ;
Zaru, R ;
Paulet, P ;
Müller, S ;
Valitutti, S .
JOURNAL OF IMMUNOLOGY, 2003, 171 (03) :1128-1132
[8]   Clonal competition inhibits the proliferation and differentiation of adoptively transferred TCR Transgenic CD4 T cells in response to infection [J].
Foulds, Kathryn E. ;
Shen, Hao .
JOURNAL OF IMMUNOLOGY, 2006, 176 (05) :3037-3043
[9]   Antigen presentation in extracellular matrix:: Interactions of T cells with dendritic cells are dynamic, short lived, and sequential [J].
Gunzer, M ;
Schäfer, A ;
Borgmann, S ;
Grabbe, S ;
Zänker, KS ;
Bröcker, EB ;
Kämpgen, E ;
Friedl, P .
IMMUNITY, 2000, 13 (03) :323-332
[10]   Naive and memory CD4+ T cell survival controlled by clonal abundance [J].
Hataye, J ;
Moon, JJ ;
Khoruts, A ;
Reilly, C ;
Jenkins, MK .
SCIENCE, 2006, 312 (5770) :114-116