Simultaneous induction of CD4 T cell tolerance and CD8 T cell immunity by semimature dendritic cells

被引:51
作者
Kleindienst, P
Wiethe, C
Lutz, MB
Brocker, T
机构
[1] Univ Munich, Inst Immunol, D-80336 Munich, Germany
[2] Univ Erlangen Nurnberg, Dept Dermatol, D-8520 Erlangen, Germany
关键词
D O I
10.4049/jimmunol.174.7.3941
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Previous studies suggested that depending on their maturation state, dendritic cells (DC) could either induce T cell tolerance (immature and semimature DC) or T cell activation (mature DC). Pretreatment of C57BL/6 mice with encephalitogenic myelin oligodendrocyte glycoprotein (MOG)(35-55) peptide-loaded semimature DC protected from MOG-induced autoimmune encephalomyelitis. This protection was mediated by IL-10-producing CD4 T cells specific for the self Ag. Here we show that semimature DC loaded with the MHC class II-restricted nonself peptide Ag (OVA) induce an identical regulatory T cell cytokine pattern. However, semimature DC loaded simultaneously with MHC class II- and MHC class I-restricted peptides, could efficiently initiate CD8 T cell responses leading to autoimmune diabetes in a TCR-transgenic adoptive transfer model. Double-peptide-loaded semimature DC also induced simultaneously in the same animal partially activated CD8 T cells with cytolytic function as well as protection from MOG-induced autoimmune encephalomyelitis. Our study suggests that the decision between tolerance and immunity not only depends on the DC, but also on the type and activation requirements of the responding T cell.
引用
收藏
页码:3941 / 3947
页数:7
相关论文
共 48 条
[41]   Evidence that a single peptide-MHC complex on a target cell can elicit a cytolytic T cell response [J].
Sykulev, Y ;
Joo, M ;
Vturina, I ;
Tsomides, TJ ;
Eisen, HN .
IMMUNITY, 1996, 4 (06) :565-571
[42]   Immune-inflammatory mechanisms in IFNγ-mediated anti-tumor activity [J].
Tannenbaum, CS ;
Hamilton, TA .
SEMINARS IN CANCER BIOLOGY, 2000, 10 (02) :113-123
[43]   Physiological β cell death triggers priming of self-reactive T cells by dendritic cells in a type-1 diabetes model [J].
Turley, S ;
Poirot, L ;
Hattori, M ;
Benoist, C ;
Mathis, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (10) :1527-1537
[44]   SERIAL TRIGGERING OF MANY T-CELL RECEPTORS BY A FEW PEPTIDE-MHC COMPLEXES [J].
VALITUTTI, S ;
MULLER, S ;
CELLA, M ;
PADOVAN, E ;
LANZAVECCHIA, A .
NATURE, 1995, 375 (6527) :148-151
[45]   Most lymphoid organ dendritic cell types are phenotypically and functionally immature [J].
Wilson, NS ;
El-Sukkari, D ;
Belz, GT ;
Smith, CM ;
Steptoe, RJ ;
Heath, WR ;
Shortman, K ;
Villadangos, JA .
BLOOD, 2003, 102 (06) :2187-2194
[46]   Direct expansion of functional CD25+ CD4+ regulatory T cells by antigen-processing dendritic cells [J].
Yamazaki, S ;
Iyoda, T ;
Tarbell, K ;
Olson, K ;
Velinzon, K ;
Inaba, K ;
Steinman, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (02) :235-247
[47]   Adherent dendritic cells expressing high levels of interleukin-10 and low levels of interleukin-12 induce antigen-specific tolerance to experimental autoimmune encephalomyelitis [J].
Yang, JS ;
Xu, LY ;
Huang, YM ;
Van Der Meide, PH ;
Link, H ;
Xiao, BG .
IMMUNOLOGY, 2000, 101 (03) :397-403
[48]   Schistosoma mansoni antigens modulate the activity of the innate immune response and prevent onset of type 1 diabetes [J].
Zaccone, P ;
Fehérvári, Z ;
Jones, FM ;
Sidobre, S ;
Kronenberg, M ;
Dunne, DW ;
Cooke, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2003, 33 (05) :1439-1449