TRYPANOSOMA-CRUZI GLUTATHIONE-BINDING PROTEINS (TCGBP) - PROTECTION INDUCED BY NATIVE PROTEINS IN AN EXPERIMENTAL-MODEL AND ANALYSIS OF THE ANTIBODY-RESPONSE

被引:11
作者
PLUMASMARTY, B
TAIBI, A
PESSOA, H
VERWAERDE, C
LOYENS, M
POMMIER, V
VELGE, P
CAPRON, A
OUAISSI, A
机构
[1] INST PASTEUR,CTR IMMUNOL & BIOL PARASITAIRE,TRYPANOSOMATIDS RES LAB,CNRS,F-59019 LILLE,FRANCE
[2] UNIV ESTADA RIO DE JANIERO,FAC CIENCIAS MED,RIO JANEIRO,RJ,BRAZIL
[3] INRA,F-37380 NOUZILLY,FRANCE
来源
RESEARCH IN IMMUNOLOGY | 1993年 / 144卷 / 08期
关键词
CHAGAS DISEASE; IGE; IGG; TRYPANOSOMA CRUZI; GLUTATHIONE; BINDING PROTEIN; IMMUNOPROTECTION; IGG ISOTYPES; BORDETELLA PERTUSSIS; ALUM; FREUNDS ADJUVANTS; MOUSE;
D O I
10.1016/S0923-2494(05)80002-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Three Trypanosoma cruzi glutathione-binding proteins (TcGBP) of 45, 30 and 25 kDa presenting glutathione S transferase activity were characterized from T. cruzi epimastigotes. We show here that immunization of mice using TcGBP and complete Freund's adjuvant (CFA) did not protect the animals against a challenge with bloodstream trypomastigotes. In contrast, immunization of mice using TcGBP in association with Bordetella pertussis plus alum (BpAl) resulted in greatly diminished parasitaemia and significantly protected the animals from lethal infection. Using TcGBP mixed with BpAI and a lower challenge dose, we obtained strongly diminished parasitaemia and 100 % protection in terms of survival. Only sera from mice immunized with TcGBP plus BpAl were able to kill trypomastigotes by complement-mediated lysis, whereas sera from mice immunized with TcGBP plus CFA did not. Interestingly, sera from mice immunized with TcGBP plus BpAl showed significant levels of specific IgE, IgG2a and IgG2b antibodies, whereas these isotypes were not detected in sera from mice immunized with TcGBP in CFA. All these levels were increased in sera of protected animals. These results demonstrate that TcGBP antigens can confer resistance to T. cruzi acute infection in mice, and suggest a possible functional role for both IgE and IgG2 isotypes in the induction of protective immunity.
引用
收藏
页码:553 / 563
页数:11
相关论文
共 34 条
[1]  
ALVES MJM, 1986, MOL BIOCHEM PARASIT, V21, P75, DOI 10.1016/0166-6851(86)90081-2
[2]  
ARAUJO FG, 1988, MEM I O CRUZ, V83, P138
[3]   ADJUVANTS FOR ANTI-PARASITE VACCINES [J].
BOMFORD, R .
PARASITOLOGY TODAY, 1989, 5 (02) :41-46
[4]   BIOLOGY OF TRYPANOSOMA-CRUZI [J].
BRENER, Z .
ANNUAL REVIEW OF MICROBIOLOGY, 1973, 27 :347-382
[5]  
BRENER Z, 1987, PARASITOL TODAY, V2, P196
[6]   IMMUNITY TO SCHISTOSOMES - PROGRESS TOWARD VACCINE [J].
CAPRON, A ;
DESSAINT, JP ;
CAPRON, M ;
OUMA, JH ;
BUTTERWORTH, AE .
SCIENCE, 1987, 238 (4830) :1065-1072
[7]  
CAPRON A, 1990, MOL ASPECTS IMMUNE R
[8]   TRYPANOSOMA-CRUZI - FIBRONECTIN PROMOTES UPTAKE OF EPIMASTIGOTE CULTURE FORMS BY HUMAN-NEUTROPHILS AND MONOCYTES [J].
CORNETTE, J ;
CAPRON, A ;
OUAISSI, MA .
INTERNATIONAL ARCHIVES OF ALLERGY AND APPLIED IMMUNOLOGY, 1988, 86 (02) :139-146
[9]  
EDELMAN R, 1980, REV INFECT DIS, V2, P370
[10]   COMPARISON OF GENES ENCODING TRYPANOSOMA-CRUZI ANTIGENS [J].
FRASCH, ACC ;
CAZZULO, JJ ;
ASLUND, L ;
PETTERSSON, U .
PARASITOLOGY TODAY, 1991, 7 (06) :148-151