Cutting edge: Cell autonomous rather than environmental factors control bacterial superantigen-induced T cell anergy in vivo

被引:8
作者
Attinger, A
Acha-Orbea, H
MacDonald, HR
机构
[1] Ludwig Inst Canc Res, Lausanne Branch, CH-1066 Epalinges, Switzerland
[2] Univ Lausanne, Inst Biochem, CH-1066 Epalinges, Switzerland
关键词
D O I
10.4049/jimmunol.165.3.1171
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Anergic T cells display a marked decrease in their ability to produce IL-2 and to proliferate in the presence of an appropriate antigenic signal. Two nonmutually exclusive classes of models have been proposed to explain the persistence of T cell anergy in vivo. While some reports indicate that anergic T cells have intrinsic defects in signaling pathways or transcriptional activities, other studies suggest that anergy is maintained by environmental "suppressor" factors such as cytokines or Abs. To distinguish between these conflicting hypotheses, we employed the well-characterized bacterial superantigen model system to evaluate in vivo the ability of a trace population of adoptively transferred naive or anergized T cells to proliferate in a naive vs anergic environment upon subsequent challenge. Our data clearly demonstrate that bacterial superantigen-induced T cell anergy is cell autonomous and independent of environmental factors.
引用
收藏
页码:1171 / 1174
页数:4
相关论文
共 27 条
[1]  
Aroeira LS, 1999, EUR J IMMUNOL, V29, P437
[2]   CLONAL ANERGY TO STAPHYLOCOCCAL ENTEROTOXIN-B IN-VIVO - SELECTIVE EFFECTS ON T-CELL SUBSETS AND LYMPHOKINES [J].
BASCHIERI, S ;
LEES, RK ;
LUSSOW, AR ;
MACDONALD, HR .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (10) :2661-2666
[3]   NEGATIVE TRANSCRIPTIONAL REGULATION IN ANERGIC T-CELLS [J].
BECKER, JC ;
BRABLETZ, T ;
KIRCHNER, T ;
CONRAD, CT ;
BROCKER, EB ;
REISFELD, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (06) :2375-2378
[4]   Transferable anergy: Superantigen treatment induces CD4(+) T cell tolerance that is reversible and requires CD4(-)CD8(-) cells and interferon gamma [J].
Cauley, LS ;
Cauley, KA ;
Shub, F ;
Huston, G ;
Swain, SL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (01) :71-81
[5]   IL-2 unresponsiveness in anergic CD4+ T cells is due to defective signaling through the common γ-chain of the IL-2 receptor [J].
Grundström, S ;
Dohlsten, M ;
Sundstedt, A .
JOURNAL OF IMMUNOLOGY, 2000, 164 (03) :1175-1184
[6]   SUPERANTIGEN-REACTIVE T-CELLS THAT DISPLAY AN ANERGIC PHENOTYPE IN-VITRO APPEAR FUNCTIONAL IN-VIVO [J].
HEEG, K ;
GAUS, H ;
GRIESE, D ;
BENDIGS, S ;
MIETHKE, T ;
WAGNER, H .
INTERNATIONAL IMMUNOLOGY, 1995, 7 (01) :105-114
[7]   MURINE CD8(+) T-CELLS THAT SPECIFICALLY DELETE AUTOLOGOUS CD4(+) T-CELLS EXPRESSING V-BETA-8 TCR - A ROLE OF THE Q-ALPHA-1 MOLECULE [J].
JIANG, H ;
WARE, R ;
STALL, A ;
FLAHERTY, L ;
CHESS, T ;
PERNIS, B .
IMMUNITY, 1995, 2 (02) :185-194
[8]   SELECTIVE ANERGY OF V-BETA-8+,CD4+ T-CELLS IN STAPHYLOCOCCUS ENTEROTOXIN B-PRIMED MICE [J].
KAWABE, Y ;
OCHI, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (04) :1065-1070
[9]  
KitagawaSakakida S, 1996, J IMMUNOL, V157, P2328
[10]   DETERMINATION OF LYMPHOCYTE DIVISION BY FLOW-CYTOMETRY [J].
LYONS, AB ;
PARISH, CR .
JOURNAL OF IMMUNOLOGICAL METHODS, 1994, 171 (01) :131-137