Implication of transforming growth factor-β1 in chagas disease myocardiopathy

被引:69
作者
Araújo-Jorge, TC
Waghabi, MC
Hasslocher-Moreno, AM
Xavier, SS
Higuchi, MD
Keramidas, M
Bailly, S
Feige, JJ
机构
[1] Laboratory of Cell Biology, Dept. of Ultrastructure Biology, Inst. of Clin. Res. Evandro Chagas, Rio de Janeiro
[2] Department of Clinical Research, Inst. of Clin. Res. Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro
[3] Service of Pathology, Heart Institute, University of São Paulo, São Paulo
[4] Équipe Mixte INSERM 105, Department of Cellular Responses, Commissariat a l'Energie Atomique, Grenoble
[5] Lab. de Biologia Celular, Dept. Ultra-Estrutura Biologia, Instituto Oswaldo Cruz, Rio de Janeiro 21045-900, Fiocruz
关键词
D O I
10.1086/345882
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cardiac dysfunction with progressive fibrosis is a hallmark of Chagas disease. To evaluate the involvement of transforming growth factor (TGF)-beta1 in this disease, TGF-beta1 levels in patients were measured at 3 stages: asymptomatic indeterminate (IND), cardiac with no or slight heart dysfunction (Card 1), and cardiac with moderate or severe heart dysfunction (Card 2). All patients had significantly higher circulating levels of TGF-beta1 than did healthy persons, and 27% of patients in the Card 1 group had higher TGF-beta1 levels than did patients in the IND group. Immunohistochemical analysis of cardiac biopsy specimens showed strong fibronectin staining in the extracellular matrix and staining for phosphorylated Smad 2 (activation of the TGF-beta1 signaling pathway) in cell nuclei. The higher levels of latent TGF-beta1 observed in patients with myocardiopathy, together with intracellular activation of the TGF-beta1 pathway and tissue fibrosis, suggest that TGF-beta1 plays an important role in Chagas disease. TGF-beta1 may represent a new target for preventive and curative treatments of Chagas disease.
引用
收藏
页码:1823 / 1828
页数:6
相关论文
共 29 条
[1]  
[Anonymous], 1991, PEPTIDE GROWTH FACTO
[2]   Smads as transcriptional co-modulators [J].
Attisano, L ;
Wrana, JL .
CURRENT OPINION IN CELL BIOLOGY, 2000, 12 (02) :235-243
[3]   Upregulation of adhesion molecules and class IHLA in the myocardium of chronic chagasic cardiomyopathy and heart allograft rejection, but not in dilated cardiomyopathy [J].
Benvenuti, LA ;
Higuchi, ML ;
Reis, MM .
CARDIOVASCULAR PATHOLOGY, 2000, 9 (02) :111-117
[4]   Influence of parasite presence on the immunologic profile of peripheral blood mononuclear cells from chagasic patients after specific drug therapy [J].
Dutra, WO ;
daLuz, ZMP ;
Cancado, JR ;
Pereira, ME ;
BrigidoNunes, RM ;
Galvao, LMC ;
Colley, DG ;
Brener, Z ;
Gazzinelli, G ;
CarvalhoParra, JF .
PARASITE IMMUNOLOGY, 1996, 18 (11) :579-585
[5]   Repeated exposure induces periportal fibrosis in Schistosoma mansoni-infected baboons:: Role of TGF-β and IL-4 [J].
Farah, IO ;
Mola, PW ;
Kariuki, TM ;
Nyindo, M ;
Blanton, RE ;
King, CL .
JOURNAL OF IMMUNOLOGY, 2000, 164 (10) :5337-5343
[6]   alpha(2)-Macroglobulin: A binding protein for transforming growth factor-beta and various cytokines [J].
Feige, JJ ;
Negoescu, A ;
Keramidas, M ;
Souchelnitskiy, S ;
Chambaz, EM .
HORMONE RESEARCH, 1996, 45 (3-5) :227-232
[7]   THE MICROBICIDAL ACTIVITY OF INTERFERON-GAMMA-TREATED MACROPHAGES AGAINST TRYPANOSOMA-CRUZI INVOLVES AN L-ARGININE-DEPENDENT, NITROGEN OXIDE-MEDIATED MECHANISM INHIBITABLE BY INTERLEUKIN-10 AND TRANSFORMING GROWTH-FACTOR-BETA [J].
GAZZINELLI, RT ;
OSWALD, IP ;
HIENY, S ;
JAMES, SL ;
SHER, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (10) :2501-2506
[8]   ANTI-TRYPANOSOMA-CRUZI AND ANTI-LAMININ ANTIBODIES IN CHAGASIC PATIENTS AFTER SPECIFIC TREATMENT [J].
GAZZINELLI, RT ;
GALVAO, LMC ;
CARDOSO, JE ;
CANCADO, JR ;
KRETTLI, AU ;
BRENER, Z ;
GAZZINELLI, G .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (09) :1795-1800
[9]   TGF-beta latency: Biological significance and mechanisms of activation [J].
Gleizes, PE ;
Munger, JS ;
Nunes, I ;
Harpel, JG ;
Mazzieri, R ;
Noguera, I ;
Rifkin, DB .
STEM CELLS, 1997, 15 (03) :190-197
[10]  
Hansen DS, 1998, SCAND J IMMUNOL, V47, P509