Characterization of the immune response to Leishmania infantum recombinant antigens

被引:34
作者
de Carvalho, LP
Soto, M
Jerônimo, S
Dondji, B
Bacellar, O
Luz, V
Orge, GO
Alonso, C
Jesus, AR
Carvalho, EM
机构
[1] Univ Fed Bahia, SErv Imunol, Hosp Univ Prof Edgard Santos, BR-40110160 Salvador, BA, Brazil
[2] UAM, CSIC, Ctr Biol Mol, Madrid, Spain
[3] Univ Fed Rio Grande Norte, Dept Bioquim, BR-59072970 Natal, RN, Brazil
[4] Univ Ngaoundere, Fac Sci, Dept Biol Sci, Ngaoundere, Cameroon
关键词
leishmaniasis; immuneregulation; IFN-gamma; KMP11;
D O I
10.1016/S1286-4579(02)00051-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Leishmaniases have a high prevalence in tropical countries. In order to improve existing diagnostic systems based on total Leishmania proteins, and to identify antigen candidates for vaccine development, an intensive search for the identification of antigens was performed using molecular biology techniques. In this study, the immune response to three L. infantum recombinant antigens was evaluated. Upon stimulation with KMP11, mononuclear cells from leishmaniasis patients produced high levels of IL-10, while a predominant IFN-gamma production could be observed in cultures stimulated with H2A and soluble Leishmania antigen. All the recombinant antigens induced very little IL-5. KMP11 decreased IFN-gamma production by 48% in cultures of peripheral blood mononuclear cells from cutaneous leishmaniasis patients who had been stimulated with soluble Leishmania antigen. Furthermore, antibodies to KMP11 were detected in the sera from all patients with visceral leishmaniasis and in the majority of the sera from patients with cutaneous leishmaniasis or individuals with asymptomatic L. chagasi infection. Thus, KMP11 is recognized by cells and sera of patients with different clinical forms of leishmaniasis, and KMP11, through IL-10 production, proved to be a potent antigen in modulating type 1 immune response. (C) 2003 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
引用
收藏
页码:7 / 12
页数:6
相关论文
共 31 条
[1]   IL-10 and IL-12 are the main regulatory cytokines in visceral leishmaniasis [J].
Bacellar, O ;
D'Oliveira, A ;
Jerônimo, S ;
Carvalho, EM .
CYTOKINE, 2000, 12 (08) :1228-1231
[2]   EVALUATION OF THE MICRO ENZYME-LINKED-IMMUNOSORBENT-ASSAY (ELISA) FOR ANTIBODIES IN AMERICAN VISCERAL LEISHMANIASIS - ANTIGEN SELECTION FOR DETECTION OF INFECTION-SPECIFIC RESPONSES [J].
BADARO, R ;
REED, SG ;
BARRAL, A ;
ORGE, G ;
JONES, TC .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1986, 35 (01) :72-78
[3]  
BOMTIM G, 1996, EXP PARASITOL, V84, P188
[4]  
BURNS JM, 1991, J IMMUNOL, V146, P742
[5]   IMMUNOLOGICAL MARKERS OF CLINICAL EVOLUTION IN CHILDREN RECENTLY INFECTED WITH LEISHMANIA-DONOVANI-CHAGASI [J].
CARVALHO, EM ;
BARRAL, A ;
PEDRALSAMPAIO, D ;
BARRALNETTO, M ;
BADARO, R ;
ROCHA, H ;
JOHNSON, WD .
JOURNAL OF INFECTIOUS DISEASES, 1992, 165 (03) :535-540
[6]   ANTIGEN-SPECIFIC IMMUNOSUPPRESSION IN VISCERAL LEISHMANIASIS IS CELL-MEDIATED [J].
CARVALHO, EM ;
BACELLAR, O ;
BARRAL, A ;
BADARO, R ;
JOHNSON, WD .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (03) :860-864
[7]   ABSENCE OF GAMMA-INTERFERON AND INTERLEUKIN-2 PRODUCTION DURING ACTIVE VISCERAL LEISHMANIASIS [J].
CARVALHO, EM ;
BADARO, R ;
REED, SG ;
JONES, TC ;
JOHNSON, WD .
JOURNAL OF CLINICAL INVESTIGATION, 1985, 76 (06) :2066-2069
[8]  
CARVALHO EM, 1985, J IMMUNOL, V135, P4144
[9]  
Castes M, 1993, Biol Res, V26, P233
[10]  
Cook JW, 2001, AM SURGEON, V67, P237