A TNF family member LIGHT transduces costimulatory signals into human T cells

被引:66
作者
Wan, XC
Zhang, J
Luo, HY
Shi, GX
Kapnik, E
Kim, S
Kanakaraj, P
Wu, JP
机构
[1] Univ Montreal, Ctr Hosp Univ Montreal, Notre Dame Hosp, Res Ctr,Lab Transplantat Immunol, Montreal, PQ H2L 4M1, Canada
[2] Univ Montreal, Ctr Hosp Univ Montreal, Notre Dame Hosp, Serv Nephrol, Montreal, PQ H2L 4M1, Canada
[3] Human Genome Sci, Rockville, MD USA
关键词
D O I
10.4049/jimmunol.169.12.6813
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
DcR3/TR6 is a secreted protein belonging to the TNFR family. It binds to Fas ligand, LIGHT, and TL1A, all of which are TNF family members. LIGHT is expressed on activated T cells. Its known receptors are TR2 and LTbetaR on the cell surface, and TR6 in solution. In the present study, we report soluble TR6-Fc or solid-phase TR6-Fc costimulated proliferation, lymphokine production, and cytotoxicity of human T cells in the presence of TCR ligation. These costimulating effects were blocked by soluble LIGHT but not by soluble Fas-Fc. TR6-Fc could also effectively costimulate gld/gld mouse T cells. We further demonstrated that TR6 bound to both Th1 and Th2 cells, according to flow cytometry, and that the association was inhibited by soluble LIGHT. Cross-linking Th1 and Th2 cells with solid-phase TR6-Fc along with a suboptimal concentration of anti-CD3 enhanced proliferation of both Th1 and Th2 cells, and augmented Th1 but not Th2 lymphokine production. These data suggest that TR6 delivers costimulation through its ligand(s) on the T cell surface, and at least the major part of such costimulation is via LIGHT.
引用
收藏
页码:6813 / 6821
页数:9
相关论文
共 41 条
[1]  
Aggarwal BB, 1996, EUR CYTOKINE NETW, V7, P93
[2]   Overexpression of M68/DcR3 in human gastrointestinal tract tumors independent of gene amplification and its location in a four-gene cluster [J].
Bai, C ;
Connolly, B ;
Metzker, ML ;
Hilliard, CA ;
Liu, XM ;
Sandig, V ;
Soderman, A ;
Galloway, SM ;
Liu, QY ;
Austin, CP ;
Caskey, CT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (03) :1230-1235
[3]   The tumor necrosis factor ligand and receptor families [J].
Bazzoni, F ;
Beutler, B .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (26) :1717-1725
[4]   A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells [J].
Black, RA ;
Rauch, CT ;
Kozlosky, CJ ;
Peschon, JJ ;
Slack, JL ;
Wolfson, MF ;
Castner, BJ ;
Stocking, KL ;
Reddy, P ;
Srinivasan, S ;
Nelson, N ;
Boiani, N ;
Schooley, KA ;
Gerhart, M ;
Davis, R ;
Fitzner, JN ;
Johnson, RS ;
Paxton, RJ ;
March, CJ ;
Cerretti, DP .
NATURE, 1997, 385 (6618) :729-733
[5]   The CD40 ligand directly activates T-lymphocytes via tyrosine phosphorylation dependent PKC activation [J].
Brenner, B ;
Koppenhoefer, U ;
LeppleWienhues, A ;
Grassme, H ;
Muller, C ;
Speer, CP ;
Lang, F ;
Gulbins, E .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 239 (01) :11-17
[6]   Evidence for a novel function of the CD40 ligand as a signalling molecule in T-lymphocytes [J].
Brenner, B ;
Koppenhoefer, U ;
Grassme, H ;
Kun, J ;
Lang, F ;
Gulbins, E .
FEBS LETTERS, 1997, 417 (03) :301-306
[7]  
Browning JL, 1997, J IMMUNOL, V159, P3288
[8]  
BUKOWSKI JF, 1995, J IMMUNOL, V154, P998
[9]  
CAYABYAB M, 1994, J IMMUNOL, V152, P1523
[10]   Engagement of CD153 (CD30 ligand) by CD30+ T cells inhibits class switch DNA recombination and antibody production in human IgD+ IgM+ B cells [J].
Cerutti, A ;
Schaffer, A ;
Goodwin, RG ;
Shah, S ;
Zan, H ;
Ely, S ;
Casali, P .
JOURNAL OF IMMUNOLOGY, 2000, 165 (02) :786-794