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恰加斯病:已知情况与所需措施——一篇背景文章

Chagas disease: what is known and what is needed--a background article.

作者信息

Coura José Rodrigues

机构信息

Laboratório de Doenças Parasitárias, Instituto Oswaldo Cruz, Fiocruz, Rio de Janeiro, 21045-900, Brasil.

出版信息

Mem Inst Oswaldo Cruz. 2007 Oct 30;102 Suppl 1:113-22. doi: 10.1590/s0074-02762007000900018.

Abstract

Chagas disease began millions of years ago as an enzootic disease of wild animals and started to be transmitted to man accidentally in the form of an anthropozoonosis when man invaded wild ecotopes. Endemic Chagas disease became established as a zoonosis over the last 200-300 years through forest clearance for agriculture and livestock rearing and adaptation of triatomines to domestic environments and to man and domestic animals as a food source. It is estimated that 15 to 16 million people are infected with Trypanosoma cruzi in Latin America and 75 to 90 million people are exposed to infection. When T. cruzi is transmitted to man through the feces of triatomines, at bite sites or in mucosa, through blood transfusion or orally through contaminated food, it invades the bloodstream and lymphatic system and becomes established in the muscle and cardiac tissue, the digestive system and phagocytic cells. This causes inflammatory lesions and immune responses, particularly mediated by CD4+, CD8+, interleukin-2 (IL) and IL-4, with cell and neuron destruction and fibrosis, and leads to blockage of the cardiac conduction system, arrhythmia, cardiac insufficiency, aperistalsis, and dilatation of hollow viscera, particularly the esophagus and colon. T. cruzi may also be transmitted from mother to child across the placenta and through the birth canal, thus causing abortion, prematurity, and organic lesions in the fetus. In immunosuppressed individuals, T. cruzi infection may become reactivated such that it spreads as a severe disease causing diffuse myocarditis and lesions of the central nervous system. Chagas disease is characterized by an acute phase with or without symptoms, and with entry point signs (inoculation chagoma or Romaña's sign), fever, adenomegaly, hepatosplenomegaly, and evident parasitemia, and an indeterminate chronic phase (asymptomatic, with normal results from electrocardiogram and x-ray of the heart, esophagus, and colon) or with a cardiac, digestive or cardiac-digestive form. There is great regional variation in the morbidity due to Chagas disease, and severe cardiac or digestive forms may occur in 10 to 50% of the cases, or the indeterminate form in the other asymptomatic cases, but with positive serology. Several acute cases have been reported from Amazon region most of them by T. cruzi I, Z3, and a hybrid ZI/Z3. We conclude this article presenting the ten top Chagas disease needs for the near future.

摘要

恰加斯病始于数百万年前,是野生动物的一种地方性动物病,当人类侵入野生生态环境时,它开始以人畜共患病的形式偶然传播给人类。在过去200 - 300年间,由于为农业和畜牧业开垦森林,以及锥蝽适应家庭环境并将人类和家畜作为食物来源,地方性恰加斯病逐渐成为一种人畜共患病。据估计,拉丁美洲有1500万至1600万人感染克氏锥虫,7500万至9000万人面临感染风险。当克氏锥虫通过锥蝽的粪便、在叮咬部位或黏膜处、通过输血或经口通过受污染食物传播给人类时,它会侵入血液循环和淋巴系统,并在肌肉和心脏组织、消化系统及吞噬细胞中定植。这会引发炎症性病变和免疫反应,尤其是由CD4 +、CD8 +、白细胞介素 - 2(IL)和IL - 4介导的反应,导致细胞和神经元破坏以及纤维化,并引发心脏传导系统阻塞、心律失常、心脏功能不全、蠕动消失以及中空脏器扩张,特别是食管和结肠。克氏锥虫也可通过胎盘和产道从母亲传播给胎儿,从而导致流产、早产以及胎儿出现器质性病变。在免疫抑制个体中,克氏锥虫感染可能会重新激活,进而发展为一种严重疾病,引发弥漫性心肌炎和中枢神经系统病变。恰加斯病的特征是急性期有症状或无症状,伴有感染部位体征(接种性恰加斯肿或罗阿尼亚征)、发热、腺肿大、肝脾肿大以及明显的寄生虫血症,还有不确定的慢性期(无症状,心电图以及心脏、食管和结肠的X光检查结果正常)或心脏型、消化型或心脏 - 消化型。恰加斯病的发病率存在很大的地区差异,10%至50%的病例可能出现严重的心脏型或消化型,其他无症状病例则可能为不确定型,但血清学检测呈阳性。亚马逊地区报告了几例急性病例,其中大多数由克氏锥虫I型、Z3型以及杂交ZI/Z3型引起。我们在本文结尾列出了近期恰加斯病最迫切需要解决的十大问题。

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