Bonney Kevin M, Engman David M
Department of Pathology, Northwestern University, Chicago, Illinois; Department of Microbiology-Immunology, Northwestern University, Chicago, Illinois.
Department of Pathology, Northwestern University, Chicago, Illinois; Department of Microbiology-Immunology, Northwestern University, Chicago, Illinois; Department of Feinberg Cardiovascular Research Institute, Northwestern University, Chicago, Illinois.
Am J Pathol. 2015 Jun;185(6):1537-47. doi: 10.1016/j.ajpath.2014.12.023. Epub 2015 Apr 7.
Chagas heart disease is an inflammatory cardiomyopathy that develops in approximately one-third of individuals infected with the protozoan parasite Trypanosoma cruzi. Since the discovery of T. cruzi by Carlos Chagas >100 years ago, much has been learned about Chagas disease pathogenesis; however, the outcome of T. cruzi infection is highly variable and difficult to predict. Many mechanisms have been proposed to promote tissue inflammation, but the determinants and the relative importance of each have yet to be fully elucidated. The notion that some factor other than the parasite significantly contributes to the development of myocarditis was hypothesized by the first physician-scientists who noted the conspicuous absence of parasites in the hearts of those who succumbed to Chagas disease. One of these factors-autoimmunity-has been extensively studied for more than half a century. Although questions regarding the functional role of autoimmunity in the pathogenesis of Chagas disease remain unanswered, the development of autoimmune responses during infection clearly occurs in some individuals, and the implications that this autoimmunity may be pathogenic are significant. In this review, we summarize what is known about the pathogenesis of Chagas heart disease and conclude with a view of the future of Chagas disease diagnosis, pathogenesis, therapy, and prevention, emphasizing recent advances in these areas that aid in the management of Chagas disease.
恰加斯心脏病是一种炎症性心肌病,约三分之一感染原生动物寄生虫克氏锥虫的个体中会发生这种疾病。自100多年前卡洛斯·恰加斯发现克氏锥虫以来,人们对恰加斯病的发病机制有了很多了解;然而,克氏锥虫感染的结果差异很大,难以预测。人们提出了许多促进组织炎症的机制,但每种机制的决定因素及其相对重要性尚未完全阐明。最早注意到死于恰加斯病的患者心脏中明显没有寄生虫的内科医生科学家们推测,除了寄生虫之外,还有其他因素对心肌炎的发展有显著影响。其中一个因素——自身免疫——已经被广泛研究了半个多世纪。尽管关于自身免疫在恰加斯病发病机制中的功能作用问题仍未得到解答,但感染期间自身免疫反应的发展显然在一些个体中发生,而且这种自身免疫可能具有致病性的影响是重大的。在这篇综述中,我们总结了关于恰加斯心脏病发病机制的已知内容,并以对恰加斯病诊断、发病机制、治疗和预防的未来展望作为结尾,强调这些领域中有助于恰加斯病管理的最新进展。