Comparative analysis of cell phenotypes in different severe clinical forms of Chagas' disease

被引:11
作者
Cardoso, GM
Morato, MJF
Gomes, JAS
Rocha, MOC
Bonfim, IP
Williams-Blangero, S
VandeBerg, JL
Reis, MR
Magalhaes, EFL
Correa-Oliveira, R
机构
[1] Fiocruz MS, Lab Imunol Celular & Mol, Ctr Pesquisas Rene Rachou, BR-30190002 Belo Horizonte, MG, Brazil
[2] Ctr Univ Newton Paiva, Belo Horizonte, MG, Brazil
[3] Univ Fed Minas Gerais, Fac Med, Curso Posgrad Med Trop, Belo Horizonte, MG, Brazil
[4] Unidade Hosp Dr Arquimedes Vieira de Brito, Posse, Go, Brazil
[5] SW Fdn Biomed Res, Dept Genet, San Antonio, TX 78284 USA
[6] Fiocruz MS, Ctr Pesquisas Goncalo Moniz, Lab Patol & Biol Mol, Salvador, BA, Brazil
[7] Univ Fed Espirito Santo, NDI, Vitoria, ES, Brazil
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2006年 / 11卷
关键词
Chagas' disease; cytokine; clinical forms; parasite; disease; blood; cell;
D O I
10.2741/1870
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The understanding of the role of the immune response in the development of gastrointestinal and cardiodigestive (CD) forms of Chagas disease has received little attention. In this paper, the commitment of each leukocyte population of peripheral blood to the production of IFNgamma, TNF-alpha, IL-12, IL-4, IL-5 and IL-10 was studied in patients with the CD form of Chagas disease. The data show that cells from patients with the CD form of the disease have distinct cytokine profiles when compared with the other clinical forms of Chagas disease and suggest that eosinophils are the major source of cytokine production in this clinical entity. The data presented in this paper demonstrate that patients with CD form can be distinguished from patients with gastrointestinal or cardiac forms of the disease by the distinct cytokine profile of peripheral blood cells.
引用
收藏
页码:1158 / 1163
页数:6
相关论文
共 14 条
[1]
Interleukin-12 stimulation of lymphoproliferative responses in Trypanosoma cruzi infection [J].
Da Silva, APG ;
Abrahamsohn, ID .
IMMUNOLOGY, 2001, 104 (03) :349-354
[2]
Innate and acquired immunity in the pathogenesis of chagas disease [J].
Golgher, D ;
Gazzinelli, RT .
AUTOIMMUNITY, 2004, 37 (05) :399-409
[3]
Evidence that development of severe cardiomyopathy in human Chagas' disease is due to a thl-specific immune response [J].
Gomes, JAS ;
Bahia-Oliveira, LMG ;
Rocha, MOC ;
Martins-Filho, OA ;
Gazzinelli, G ;
Correa-Oliveira, R .
INFECTION AND IMMUNITY, 2003, 71 (03) :1185-1193
[4]
Decreased CD4+ circulating T lymphocytes in patients with gastrointestinal Chagas disease [J].
Lemos, EM ;
Reis, DD ;
Adad, SJ ;
Silva, GC ;
Crema, E ;
Correa-Oliveira, R .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1998, 88 (02) :150-155
[5]
OLIVEIRA RB, 1998, AM J GASTROENTEROL, V93, P884
[6]
Phenotypic characterization of the inflammatory cells in chagasic mega-oesophagus [J].
Reis, DD ;
Lemos, EM ;
Silva, GC ;
Adad, SJ ;
McCurley, T ;
Correa-Oliveira, R ;
Machado, CRS .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 2001, 95 (02) :177-178
[7]
Gastrointestinal eosinophils [J].
Rothenberg, ME ;
Mishra, A ;
Brandt, EB ;
Hogan, SP .
IMMUNOLOGICAL REVIEWS, 2001, 179 :139-155
[8]
Differential expression of systemic cytokine profiles in Chagas' disease is associated with endemicity of Trypanosoma cruzi infections [J].
Samudio, M ;
Montenegro-James, S ;
de Cabral, M ;
Martinez, J ;
de Arias, AR ;
Woroniecky, O ;
James, MA .
ACTA TROPICA, 1998, 69 (02) :89-97
[9]
Cytokine responses in Trypanosoma cruzi-infected children in Paraguay [J].
Samudio, M ;
Montenegro-James, S ;
Cabral, M ;
Martinez, J ;
De Arias, AR ;
James, MA .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1998, 58 (01) :119-121
[10]
The physiological and pathophysiological roles of eosinophils in the gastrointestinal tract [J].
Straumann, A ;
Simon, HU .
ALLERGY, 2004, 59 (01) :15-25