Co-stimulation of antigen-specific CD4 T cells by 4-1BB ligand

被引:11
作者
Gramaglia, I
Cooper, D
Miner, KT
Kwon, BS
Croft, M
机构
[1] La Jolla Inst Allergy & Immunol, Div Immunochem, San Diego, CA 92121 USA
[2] Indiana Univ, Sch Med, Dept Microbiol & Immunol, Indianapolis, IN 46202 USA
关键词
4-1BB; 4-1BB ligand; CD4 T cell; co-stimulation;
D O I
10.1002/1521-4141(200002)30:2<392::AID-IMMU392>3.0.CO;2-H
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
4-1BB is a member of the TNF receptor family predominantly expressed on activated T cells, and binds an inducible ligand found on B cells, macrophages and dendritic cells. Whereas ligation of 4-1BB has been shown to enhance response of purified CD8 T cells to mitogens, and to augment NK activity and generation of cytotoxic T lymphocytes in vivo, there are little direct data on 4-1BB action during CD4 responses. Using pigeon cytochrome c-presenting fibroblast antigen-presenting cells transfected with 4-1BB ligand (4-1BBL), we show that engaging 4-1BB on naive CD4 cells promotes proliferation, cell cycle progression and IL-2 secretion, and suppresses cell death, all to a similar extent as B7-1 engagement of CD28. In addition, 4-1BBL synergizes with B7 and ICAM to enhance naive CD4 proliferation when antigen is limiting. 4-1BBL alone, and to a greater extent with 87, also augmented IL-2 secretion resting antigen-experienced CD4 cells, as typified by T helper clones, whereas short-term effector cells showed similar levels of proliferation and cytokine secretion regardless of whether 4-1BB was engaged. A major role in augmenting lFN-gamma, IL-4 or IL-5 was not demonstrated. Blocking studies with activated B cells presenting antigen showed that 4-1BB participates in promoting IL-2 production by resting CD4 cells, confirming that 4-1BBL can play a role in antigen-specific CD4 T cell responses.
引用
收藏
页码:392 / 402
页数:11
相关论文
共 43 条
[1]
MOLECULAR AND BIOLOGICAL CHARACTERIZATION OF HUMAN 4-1BB AND ITS LIGAND [J].
ALDERSON, MR ;
SMITH, CA ;
TOUGH, TW ;
DAVISSMITH, T ;
ARMITAGE, RJ ;
FALK, B ;
ROUX, E ;
BAKER, E ;
SUTHERLAND, GR ;
DIN, WS ;
GOODWIN, RG .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (09) :2219-2227
[2]
Transfected Drosophila cells as a probe for defining the minimal requirements for stimulating unprimed CD8(+) T cells [J].
Cai, ZL ;
Brunmark, A ;
Jackson, MR ;
Loh, D ;
Peterson, PA ;
Sprent, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14736-14741
[3]
CAYABYAB M, 1994, J IMMUNOL, V152, P1523
[4]
Chu NR, 1997, J IMMUNOL, V158, P3081
[5]
RESPONSE OF NAIVE ANTIGEN-SPECIFIC CD4+ T-CELLS INVITRO - CHARACTERISTICS AND ANTIGEN-PRESENTING CELL REQUIREMENTS [J].
CROFT, M ;
DUNCAN, DD ;
SWAIN, SL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (05) :1431-1437
[6]
CROFT M, 1995, J IMMUNOL, V154, P4269
[7]
Croft M, 1997, J IMMUNOL, V159, P3257
[8]
Accessory molecule and costimulation requirements for CD4 T cell response [J].
Croft, M ;
Dubey, C .
CRITICAL REVIEWS IN IMMUNOLOGY, 1997, 17 (01) :89-118
[9]
Curtsinger JM, 1998, J IMMUNOL, V160, P3236
[10]
ROLE OF 4-1BB-LIGAND IN COSTIMULATION OF T-LYMPHOCYTE GROWTH AND ITS UP-REGULATION ON M12 B-LYMPHOMAS BY CAMP [J].
DEBENEDETTE, MA ;
CHU, NR ;
POLLOK, KE ;
HURTADO, J ;
WADE, WF ;
KWON, BS ;
WATTS, TH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (03) :985-992