Tnf/tnfr family members in costimulation of T cell responses

被引:1067
作者
Watts, TH [1 ]
机构
[1] Univ Toronto, Dept Immunol, Toronto, ON M5S 1A8, Canada
关键词
survival signaling; T effector cell; T cell memory;
D O I
10.1146/annurev.immunol.23.021704.115839
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Several members of the tumor necrosis factor receptor (TNFR) family function after initial T cell activation to sustain T cell responses. This review focuses on CD27,4-1BB (CD137), OX40 (CD134), HVEM, CD30, and GITR, all of which can have costimulatory effects on T cells. The effects of these costimulatory TNFR family members can often be functionally, temporally, or spatially segregated from those of CD28 and from each other. The sequential and transient regulation of T cell activation/survival signals by different costimulators may function to allow longevity of the response while maintaining tight control of T cell survival. Depending on the disease condition, stimulation via costimulatory TNFR family members can exacerbate or ameliorate disease. Despite these complexities, stimulation or blockade of TNFR family costimulators shows promise for several therapeutic applications, including cancer, infectious disease, transplantation, and autoimmunity.
引用
收藏
页码:23 / 68
页数:46
相关论文
共 321 条
[91]  
Guinn B, 1999, J IMMUNOL, V162, P5003
[92]   4-1BBL enhances anti-tumor responses in the presence or absence of CD28 but CD28 is required for protective immunity against parental tumors [J].
Guinn, BA ;
Bertram, EM ;
DeBenedette, MA ;
Berinstein, NL ;
Watts, TH .
CELLULAR IMMUNOLOGY, 2001, 210 (01) :56-65
[93]   Identification of a new member of the tumor necrosis factor family and its receptor, a human ortholog of mouse GITR [J].
Gurney, AL ;
Marsters, SA ;
Huang, A ;
Pitti, RM ;
Mark, M ;
Baldwin, DT ;
Gray, AM ;
Dowd, P ;
Brush, J ;
Heldens, S ;
Schow, P ;
Goddard, AD ;
Wood, WI ;
Baker, KP ;
Godowski, PJ ;
Ashkenazi, A .
CURRENT BIOLOGY, 1999, 9 (04) :215-218
[94]   In vivo stimulation of CD137 broadens primary antiviral CD8+ T cell responses [J].
Halstead, ES ;
Mueller, YM ;
Altman, JD ;
Katsikis, PD .
NATURE IMMUNOLOGY, 2002, 3 (06) :536-541
[95]   Evidence that human CD8+CD45RA+CD27- cells are induced by antigen and evolve through extensive rounds of division [J].
Hamann, D ;
Kostense, S ;
Wolthers, KC ;
Otto, SA ;
Baars, PA ;
Miedema, F ;
van Lier, RAW .
INTERNATIONAL IMMUNOLOGY, 1999, 11 (07) :1027-1033
[96]   TCR-independent CD30 signaling selectively induces IL-13 production via a TNF receptor-associated factor/p38 mitogen-activated protein kinase-dependent mechanism [J].
Harlin, H ;
Podack, E ;
Boothby, M ;
Alegre, ML .
JOURNAL OF IMMUNOLOGY, 2002, 169 (05) :2451-2460
[97]   Herpesvirus entry mediator ligand (HVEM-L), a novel ligand for HVEM/TR2, stimulates proliferation of T cells and inhibits HT29 cell growth [J].
Harrop, JA ;
McDonnell, PC ;
Brigham-Burke, M ;
Lyn, SD ;
Minton, J ;
Tan, KB ;
Dede, K ;
Spampanato, J ;
Silverman, C ;
Hensley, P ;
DiPrinzio, R ;
Emery, JG ;
Deen, K ;
Eichman, C ;
Chabot-Fletcher, M ;
Truneh, A ;
Young, PR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (42) :27548-27556
[98]  
Harrop JA, 1998, J IMMUNOL, V161, P1786
[99]   Functional CD137 receptors are expressed by eosinophils from patients with IgE-mediated allergic responses but not by eosinophils from patients with non-IgE-mediated eosinophilic disorders [J].
Heinisch, IVWM ;
Bizer, C ;
Volgger, W ;
Simon, HU .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2001, 108 (01) :21-28
[100]   CD27 promotes survival of activated T cells and complements CD28 in generation and establishment of the effector T cell pool [J].
Hendricks, J ;
Xiao, YL ;
Borst, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (09) :1369-1380