Pathogenesis of chronic Chagas heart disease

被引:550
作者
Marin-Neto, Jose Antonio
Cunha-Neto, Edecio
Maciel, Benedito C.
Simoes, Marcus V.
机构
[1] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Internal Med, Div Cardiol, Ribeirao Preto, Brazil
[2] Univ Sao Paulo, Inst Heart, InCor, Sao Paulo, Brazil
[3] Millenium Inst Conselho Nacl Pesquisa, Inst Invest Immunol, Sao Paulo, Brazil
关键词
autonomic nervous system; cardiomyopathy; Chagas disease; immune system; inflammation; microcirculation; Valsalva maneuver;
D O I
10.1161/CIRCULATIONAHA.106.624296
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - Chagas disease remains a significant public health issue and a major cause of morbidity and mortality in Latin America. Despite nearly 1 century of research, the pathogenesis of chronic Chagas cardiomyopathy is incompletely understood, the most intriguing challenge of which is the complex host-parasite interaction. Methods and Results - A systematic review of the literature found in MEDLINE, EMBASE, BIREME, LILACS, and SCIELO was performed to search for relevant references on pathogenesis and pathophysiology of Chagas disease. Evidence from studies in animal models and in anima nobile points to 4 main pathogenetic mechanisms to explain the development of chronic Chagas heart disease: autonomic nervous system derangements, microvascular disturbances, parasite-dependent myocardial aggression, and immune-mediated myocardial injury. Despite its prominent peculiarities, the role of autonomic derangements and microcirculatory disturbances is probably ancillary among causes of chronic myocardial damage. The pathogenesis of chronic Chagas heart disease is dependent on a low-grade but incessant systemic infection with documented immune-adverse reaction. Parasite persistence and immunological mechanisms are inextricably related in the myocardial aggression in the chronic phase of Chagas heart disease. Conclusions - Most clinical studies have been performed in very small number of patients. Future research should explore the clinical potential implications and therapeutic opportunities of these 2 fundamental underlying pathogenetic mechanisms.
引用
收藏
页码:1109 / 1123
页数:15
相关论文
共 152 条
  • [1] Molecular mimicry between cardiac myosin and Trypanosoma cruzi antigen B13: identification of a B13-driven human T cell clone that recognizes cardiac myosin
    Abel, LCJ
    Kalil, J
    CunhaNeto, E
    [J]. BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 1997, 30 (11) : 1305 - 1308
  • [2] Chronic Chagas' disease cardiomyopathy patients display an increased IFN-γ response to Trypanosoma cruzi infection
    Abel, LCJ
    Rizzo, LV
    Ianni, B
    Albuquerque, F
    Bacal, F
    Carrara, D
    Bocchi, EA
    Teixeira, HC
    Mady, C
    Kalil, J
    Cunha-Neto, E
    [J]. JOURNAL OF AUTOIMMUNITY, 2001, 17 (01) : 99 - 107
  • [3] Neuron count reevaluation in the myenteric plexus of chagasic megacolon after morphometric neuron analysis
    Adad, SJ
    Cançado, CG
    Etchebehere, RM
    Teixeira, VPA
    Gomes, UA
    Chapadeiro, E
    Lopes, ER
    [J]. VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY, 2001, 438 (03): : 254 - 258
  • [4] Trypanosoma cruzi modulates the profile of memory CD8+ T cells in chronic Chagas' disease patients
    Albareda, MC
    Laucella, SA
    Alvarez, MG
    Armenti, AH
    Bertochi, G
    Tarleton, RL
    Postan, M
    [J]. INTERNATIONAL IMMUNOLOGY, 2006, 18 (03) : 465 - 471
  • [5] ALCANTARA F G D, 1970, Revista Goiana de Medicina, V16, P159
  • [6] Amorim D D, 1995, Sao Paulo Med J, V113, P772
  • [7] AMORIM DS, 1982, MAYO CLIN PROC, V57, P48
  • [8] EFFECTS OF ACUTE ELEVATION IN BLOOD PRESSURE AND OF ATROPINE ON HEART RATE IN CHAGAS DISEASE - A PRELIMINARY REPORT
    AMORIM, DS
    GODOY, RA
    MANCO, JC
    TANAKA, A
    GALLO, L
    [J]. CIRCULATION, 1968, 38 (02) : 289 - &
  • [9] AMORIM DS, 1982, BRIT HEART J, V47, P11
  • [10] AMORIM DS, 1973, ACTA CARDIOL, V28, P4311