TSST-1 induces Th1 or Th2 differentiation in naive CD4+T cells in a dose- and APC-dependent manner

被引:13
作者
Brandt, K [1 ]
Van der Bosch, J [1 ]
Fliegert, R [1 ]
Gehring, S [1 ]
机构
[1] Med Clin Res Ctr Borstel, Div Expt Immunopharmacol, D-23845 Borstel, Germany
关键词
D O I
10.1046/j.1365-3083.2002.01170.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Superantigens are potent activators of the immune system, causing a variety of diseases, ranging from food poisoning to septic shock. Here, we examined the effects of different toxic shock syndrome toxin 1 (TSST-1) concentrations on the activation, proliferation and synthesis of interferon-gamma (IFN-gamma) and interleukin-4 (IL-4) in purified naive human CD4(+) T cells in a serum-free in vitro system. TSST-1 given in low doses (1-10 pg/ml) generates a pronounced T helper 2 (Th2)-like cytokine profile, characterized by elevated IL-4-expressing T-cell populations and reduced IFN-gamma-producing populations, whereas higher doses (100 pg/ml) induce a Th1-like profile, with increased expression of IFN-gamma and reduced expression of IL-4. These patterns were even more pronounced by adding exogenous cytokines like IL-12 and IL-4 and by the type of antigen-presenting cells (APCs). Thus, B cells induced Th2 shifts, whereas monocytes favoured Th1 induction. Moreover, IL-12 in conditions with B cells counteracted their Th2 bias. Interestingly, in purified naive T-cell cultures, containing a small population of HLA-DR+ T cells, Th1/Th2 differentiation can be induced by TSST-1 too. There, Th-cell polarization is strongly dependent on TSST-1 concentration, indicating that this is a key parameter in regulating the differentiation of T cells. In conclusion, our data show that Th1/Th2 differentiation of TSST-1-stimulated naive T cells is controlled by the type of APCs, and in APC-depleted cultures, it depends on the presence of HLA-DR+ cells and TSST-1 concentration.
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收藏
页码:572 / 579
页数:8
相关论文
共 32 条
[21]   THE STAPHYLOCOCCAL ENTEROTOXINS AND THEIR RELATIVES [J].
MARRACK, P ;
KAPPLER, J .
SCIENCE, 1990, 248 (4956) :705-711
[22]   Requirement of CD28-CD86 co-stimulation in the interaction between antigen-primed T helper type 2 and B cells [J].
Nakajima, A ;
Watanabe, N ;
Yoshino, S ;
Yagita, H ;
Okumura, K ;
Azuma, M .
INTERNATIONAL IMMUNOLOGY, 1997, 9 (05) :637-644
[23]   One cause for the apparent inability of human T cell clones to function as professional superantigen-presenting cells is autoactivation [J].
Nisini, R ;
Fattorossi, A ;
Ferlini, C ;
DAmelio, R .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (04) :797-803
[24]   Kinetic discrimination in T-cell activation [J].
Rabinowitz, JD ;
Beeson, C ;
Lyons, DS ;
Davis, MM ;
McConnell, HM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (04) :1401-1405
[25]   Induction of a cytokine network by superantigens with parallel TH1 and TH2 stimulation [J].
Rink, L ;
Luhm, J ;
Koester, M ;
Kirchner, H .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 1996, 16 (01) :41-47
[26]   The possible role of bacterial superantigens in the pathogenesis of autoimmune disorders [J].
Schiffenbauer, J ;
Soos, J ;
Johnson, H .
IMMUNOLOGY TODAY, 1998, 19 (03) :117-120
[27]   INTERLEUKIN-4 PRODUCTION BY CD4(+) T-CELLS FROM ALLERGIC INDIVIDUALS IS MODULATED BY ANTIGEN CONCENTRATION AND ANTIGEN-PRESENTING CELL-TYPE [J].
SECRIST, H ;
DEKRUYFF, RH ;
UMETSU, DT .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (03) :1081-1089
[28]   TOXIC-SHOCK SYNDROME IN MENSTRUATING WOMEN - ASSOCIATION WITH TAMPON USE AND STAPHYLOCOCCUS-AUREUS AND CLINICAL-FEATURES IN 52 CASES [J].
SHANDS, KN ;
SCHMID, GP ;
DAN, BB ;
BLUM, D ;
GUIDOTTI, RJ ;
HARGRETT, NT ;
ANDERSON, RL ;
HILL, DL ;
BROOME, CV ;
BAND, JD ;
FRASER, DW .
NEW ENGLAND JOURNAL OF MEDICINE, 1980, 303 (25) :1436-1442
[29]  
Tao X, 1997, J IMMUNOL, V158, P4237
[30]  
Torres MJ, 1998, CLIN EXP ALLERGY, V28, P1264