Comparative study of the presence of Trypanosoma cruzi kDNA inflammation and denervation in chagasic patients with and without megaesophagus

被引:45
作者
da Silveira, ABM
Arantes, RME
Vago, AR
Lemos, EM
Adad, SJ
Correa-Oliveira, R
Reis, DD
机构
[1] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Morfol, BR-31270901 Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Gen Pathol, Belo Horizonte, MG, Brazil
[3] UFES, Dept Pathol, Vitoria, Espirito Santo, Brazil
[4] Med Sch Triangulo Uberaba, Dept Pathol, Uberaba, MG, Brazil
[5] Fiocruz MS, Ctr Pesquisas Rene Rachou, Belo Horizonte, MG, Brazil
关键词
Trypanosoma cruzi; kDNA; myenteric plexus; inflammatory cells;
D O I
10.1017/S0031182005008061
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Neuronal lesions have been considered the hallmark of chagasic megaesophagus, but the role of Trypanosoma cruzi. and the participation of the inflammatory cells in this process are still debated. In the present study we counted neurons in the oesophagus from patients with and without megaesophagus and further examined these samples for the presence of parasite kDNA and cells with cytolytic potential (Natural Killer cells, cytotoxic lymphocytes and macrophages). The presence of parasite kDNA was demonstrated in 100% of cases with megaesophagus and in 60% of patients without megaesophagus. When analysed for the number Of neurons, the patients without megaesophagus could be classified into 2 groups, as having normal or a decreased number of neurons. The former group did not show any inflammatory process, but interestingly, all patients without megaesophagus presenting decreased number of neurons also presented both parasite kDNA and inflammatory process in the organ. We further observed that the numbers of cytotoxic cells in the myenteric plexus region inversely correlate with the number of neurons. These data together strongly Suggest that chronic lesions in chagasic megaesophagus might be a consequence of immune-mediated mechanisms, that last until the chronic phase of infection, and are dependent on the persistence of parasite in the host's tissue.
引用
收藏
页码:627 / 634
页数:8
相关论文
共 30 条
[1]   CONTRIBUTION TO THE STUDY OF THE PATHOLOGY AND PATHOGENESIS OF THE CHAGASIC MEGAESOPHAGUS [J].
ADAD, SJ ;
ANDRADE, DCD ;
LOPES, ER ;
CHAPADEIRO, E .
REVISTA DO INSTITUTO DE MEDICINA TROPICAL DE SAO PAULO, 1991, 33 (06) :443-450
[2]   CONSTRUCTION AND USE OF A MULTI-COMPETITOR GENE FOR QUANTITATIVE RT-PCR USING EXISTING PRIMER SETS [J].
BENAVIDES, GR ;
HUBBY, B ;
GROSSE, WM ;
MCGRAW, RA ;
TARLETON, RL .
JOURNAL OF IMMUNOLOGICAL METHODS, 1995, 181 (02) :145-156
[3]   Clinical evolution and morbi-mortality in Chagas disease [J].
Chapadeiro, E .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 1999, 94 :309-310
[4]   Cell-mediated immune response in megacolon from patients with chronic Chagas' disease [J].
Corbett, CEP ;
Ribeiro, U ;
Prianti, MDG ;
Habr-Gama, A ;
Okumara, M ;
Gama-Rodrigues, J .
DISEASES OF THE COLON & RECTUM, 2001, 44 (07) :993-998
[5]   CHAGASIC CARDIOPATHY - DEMONSTRATION OF A SERUM GAMMA-GLOBULIN FACTOR WHICH REACTS WITH ENDOCARDIUM AND VASCULAR STRUCTURES [J].
COSSIO, PM ;
DIEZ, C ;
SZARFMAN, A ;
KREUTZER, E ;
CANDIOLO, B ;
ARANA, RM .
CIRCULATION, 1974, 49 (01) :13-21
[6]  
de Oliveira RB, 1998, AM J GASTROENTEROL, V93, P884, DOI 10.1111/j.1572-0241.1998.270_r.x
[7]   Acute Chagas' disease:: immunohistochemical characteristics of T cell infiltrate and its relationship with T-cruzi parasitic antigens. [J].
Fuenmayor, C ;
Higuchi, ML ;
Carrasco, H ;
Parada, H ;
Gutierrez, P ;
Aiello, V ;
Palomino, S .
ACTA CARDIOLOGICA, 2005, 60 (01) :33-37
[8]   Trypanosoma cruzi:: Optimization of polymerase chain reaction for detection in human blood [J].
Gomes, ML ;
Macedo, AM ;
Vago, AR ;
Pena, SDJ ;
Galvao, LMC ;
Chiari, E .
EXPERIMENTAL PARASITOLOGY, 1998, 88 (01) :28-33
[9]   Interleukin-12 but not interleukin-18 is required for immunity to Trypanosoma cruzi in mice [J].
Graefe, SEB ;
Jacobs, T ;
Gaworski, I ;
Klauenberg, U ;
Steeg, C ;
Fleischer, B .
MICROBES AND INFECTION, 2003, 5 (10) :833-839
[10]   Type 1 immunity provides optimal protection against both mucosal and systemic Trypanosoma cruzi challenges [J].
Hoft, DF ;
Eickhoff, CS .
INFECTION AND IMMUNITY, 2002, 70 (12) :6715-6725