CD4 T cells integrate signals delivered during successive DC encounters in vivo

被引:134
作者
Celli, S [1 ]
Garcia, Z [1 ]
Bousso, P [1 ]
机构
[1] Inst Pasteur, INSERM 668, Dept Immunol, F-75015 Paris, France
关键词
D O I
10.1084/jem.20051018
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
The cellular mode of T cell priming in vivo remains to be characterized fully. We investigated the fate of T cell-dendritic cell ( DC) interactions in the late phase of T cell activation in the lymph node. In general, CD4 T cells detach from DCs before undergoing cell division. Using a new approach to track the history of antigen ( Ag)-recognition events, we demonstrated that activated/divided T cells reengage different DCs in an Ag-specific manner. Two-photon imaging of intact lymph nodes suggested that T cells could establish prolonged interactions with DCs at multiple stages during the activation process. Importantly, signals that are delivered during subsequent DC contacts are integrated by the T cell and promote sustained IL-2R alpha expression and IFN-gamma production. Thus, repeated encounters with Ag-bearing DCs can occur in vivo and modulate CD4 T cell differentiation programs.
引用
收藏
页码:1271 / 1278
页数:8
相关论文
共 33 条
[1]
Repeated antigen exposure is necessary for the differentiation, but not the initial proliferation, of naive CD4+ T cells [J].
Bajénoff, M ;
Wurtz, O ;
Guerder, S .
JOURNAL OF IMMUNOLOGY, 2002, 168 (04) :1723-1729
[2]
Dynamic behavior of T cells and thymocytes in lymphoid organs as revealed by two-photon microscopy [J].
Bousso, P ;
Robey, EA .
IMMUNITY, 2004, 21 (03) :349-355
[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]
Visualizing the first 50 Hr of the primary immune response to a soluble antigen [J].
Catron, DM ;
Itano, AA ;
Pape, KA ;
Mueller, DL ;
Jenkins, MK .
IMMUNITY, 2004, 21 (03) :341-347
[5]
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
[6]
T cell fitness determined by signal strength [J].
Gett, AV ;
Sallusto, F ;
Lanzavecchia, A ;
Geginat, J .
NATURE IMMUNOLOGY, 2003, 4 (04) :355-360
[7]
Are major histocompatibility complex molecules involved in the survival of naive CD4+ T cells? [J].
Grandjean, I ;
Duban, L ;
Bonney, EA ;
Corcuff, E ;
Di Santo, JP ;
Matzinger, P ;
Lantz, O .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (07) :1089-1102
[8]
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
[9]
Dynamic changes during the immune response in T cell-antigen-presenting cell clusters isolated from lymph nodes [J].
Hommel, M ;
Kyewski, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (03) :269-280
[10]
A Bcl-2-dependent molecular timer regulates the lifespan and immunogenicity of dendritic cells [J].
Hou, WS ;
Van Parijs, L .
NATURE IMMUNOLOGY, 2004, 5 (06) :583-589