T cell receptor V beta repertoire in the thymus and spleen of mice infected with Trypanosoma cruzi

被引:15
作者
Cardoni, RL
Antunez, MI
Orn, A
Gronvik, KO
机构
[1] KAROLINSKA INST,MICROBIOL & TUMORBIOL CTR,STOCKHOLM,SWEDEN
[2] NATL VET INST,LAB VACCINE RES,S-75007 UPPSALA,SWEDEN
关键词
D O I
10.1006/cimm.1996.0114
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The T cell receptor (TCR) V beta repertoire was studied in BALB/c, CBA/HJ, and CBA/J mice experimentally infected with Trypanosoma cruzi. The percentage of expression of 14 V beta chains of the variable domain of the TCR in the thymus and spleen was evaluated. In the thymus of acutely infected BALB/c and CBA/HJ mice there was an increase in the expression of positively selected V beta chains, without modifications in the negatively selected V beta families. These changes in the V beta chains usage in the thymus paralleled the enrichment of CD4(+) and CD8(+) single-positive T cells. During the acute infection, several changes were observed in the peripheral expression of V beta families, such as of V beta 6 in BALB/c (a 36% increase in CD8(+) T cells of the corresponding levels of V beta), of V beta 8 in CBA/HJ (a 37% decrease in CD8(+) cells), and of V beta chains 8 and 14 in CBA/J mice (V beta 14(+)CD4(+) cells increased 19%, and V beta 8 expression decreased 19 and 33% in CD4(+) and CD8(+) cells, respectively). In chronically infected BALB/c and CBA/HJ mice, no change in the V beta families was observed, neither in the thymus nor in the spleen. In acutely infected mice, the alterations of the peripheral expression of positively selected V beta families could be due to the stimulation by T. cruzi antigens and/or cytokines; the homeostatic mechanism/s that maintains the selection of the TCR V beta repertoire did not seem to be severely affected during the infections. (C) 1996 Academic Press, Inc.
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页码:238 / 245
页数:8
相关论文
共 46 条
[1]  
AIKAWA M, 1980, MALARIA, V2, P75
[3]   A DIFFERENTIAL-AVIDITY MODEL FOR T-CELL SELECTION [J].
ASHTONRICKARDT, PG ;
TONEGAWA, S .
IMMUNOLOGY TODAY, 1994, 15 (08) :362-366
[4]   TRYPANOSOMA-CRUZI - EARLY RESISTANCE INDUCED BY CULTURE-DERIVED TRYPOMASTIGOTES [J].
CAMARGO, IJB ;
ARAUJO, PMF ;
SAKURADA, JK ;
STACHMACHADO, DR ;
RANGEL, HA .
EXPERIMENTAL PARASITOLOGY, 1991, 73 (03) :260-268
[5]   AN AGE-RELATED GAMMA-DELTA T-CELL SUPPRESSOR ACTIVITY CORRELATES WITH THE OUTCOME OF AUTOIMMUNITY IN EXPERIMENTAL TRYPANOSOMA-CRUZI INFECTION [J].
CARDILLO, F ;
FALCAO, RP ;
ROSSI, MA ;
MENGEL, J .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (10) :2597-2605
[6]   THE THYMUS IN PREGNANCY - THE INTERPLAY OF NEURAL, ENDOCRINE AND IMMUNE INFLUENCES [J].
CLARKE, AG ;
KENDALL, MD .
IMMUNOLOGY TODAY, 1994, 15 (11) :545-551
[7]   T-CELL ANTIGEN RECEPTOR GENES AND T-CELL RECOGNITION [J].
DAVIS, MM ;
BJORKMAN, PJ .
NATURE, 1988, 334 (6181) :395-402
[8]  
DEMORAES MCL, 1992, IMMUNOLOGY, V77, P95
[9]  
DEMORAES MCL, 1994, INT IMMUNOL, V6, P387
[10]   TOXOPLASMA-GONDII POSSESSES A SUPERANTIGEN ACTIVITY THAT SELECTIVELY EXPANDS MURINE T-CELL RECEPTOR V-BETA-5-BEARING CD8+ LYMPHOCYTES [J].
DENKERS, EY ;
CASPAR, P ;
SHER, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (03) :985-994