Instruction of naive CD4+ T cells by polarized CD4+ T cells within dendritic cell clusters

被引:15
作者
Creusot, RJ
Biswas, JS
Thomsen, LL
Tite, JP
Mitchison, NA
Chain, BM
机构
[1] UCL, Windeyer Inst Med Sci, Dept Immunol & Mol Pathol, London, England
[2] GlaxoSmithKline Inc, Dept Gene & Prot Therapeut, Stevenage, Herts, England
关键词
Th1/Th2; cell; particle-mediated DNA delivery; CD4(+) T cell cooperation;
D O I
10.1002/eji.200323811
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cooperation between CD4(+) T cells can enhance the response and modulate the cytokine profile, and defining these parameters has become a major issue for multivalent-vaccine strategies. We explored cooperation using adoptive transfer of two populations of TCR transgenic T cells of different specificity. One was transferred without prior activation, whereas the second was activated for five days by antigen stimulation under polarizing culture conditions. Both populations were transferred into a single adoptive host and then primed by particle-mediated DNA delivery. Polarized Th1 cells (inducers) raised the frequency of IFN-gamma(+) cells within a naive (target) population, whereas Th2 inducers raised the frequency of IL-4(+) and reduced that of IL-2(+) cells. These effects were obtained when the genes for both antigens were on the same particle, favoring presentation by the same dendritic cell, but not when on different particles delivered to different dendritic cells. Autonomy of DC clusters allows linked sets of antigens (e.g. from a single pathogen) to maintain cytokine bias, but allows other independent responses, each with their own set of autonomous clusters.
引用
收藏
页码:1686 / 1696
页数:11
相关论文
共 51 条
[1]   The CCR7 ligand ELC (CCL19) is transcytosed in high endothelial venules and mediates T cell recruitment [J].
Baekkevold, ES ;
Yamanaka, T ;
Palframan, RT ;
Carlsen, HS ;
Reinholt, FP ;
von Andrian, UH ;
Brandtzaeg, P ;
Haraldsen, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (09) :1105-1111
[2]  
Ben-Sasson SZ, 2000, EUR J IMMUNOL, V30, P1308, DOI 10.1002/(SICI)1521-4141(200005)30:5<1308::AID-IMMU1308>3.0.CO
[3]  
2-I
[4]   Help for cytotoxic-T-cell responses is mediated by CD40 signalling [J].
Bennett, SRM ;
Carbone, FR ;
Karamalis, F ;
Flavell, RA ;
Miller, JFAP ;
Heath, WR .
NATURE, 1998, 393 (6684) :478-480
[5]   ENTRY OF NAIVE CD4 T-CELLS INTO PERIPHERAL LYMPH-NODES REQUIRES L-SELECTIN [J].
BRADLEY, LM ;
WATSON, SR ;
SWAIN, SL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (06) :2401-2406
[6]   Ligation of CD40 on dendritic cells triggers production of high levels of interleukin-12 and enhances T cell stimulatory capacity: T-T help via APC activation [J].
Cella, M ;
Scheidegger, D ;
PalmerLehmann, K ;
Lane, P ;
Lanzavecchia, A ;
Alber, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (02) :747-752
[7]  
Chao CC, 1997, J IMMUNOL, V159, P1686
[8]   Enhanced secretion of IFN-γ by activated Th1 cells occurs via reverse signaling through TNF-related activation-induced cytokine [J].
Chen, NJ ;
Huang, MW ;
Hsieh, SL .
JOURNAL OF IMMUNOLOGY, 2001, 166 (01) :270-276
[9]   Cross-priming as a predominant mechanism for inducing CD8+ T cell responses in gene gun DNA immunization [J].
Cho, JH ;
Youn, JW ;
Sung, YC .
JOURNAL OF IMMUNOLOGY, 2001, 167 (10) :5549-5557
[10]   DNA-based immunization by in vivo transfection of dendritic cells [J].
Condon, C ;
Watkins, SC ;
Celluzzi, CM ;
Thompson, K ;
Falo, LD .
NATURE MEDICINE, 1996, 2 (10) :1122-1128