Bustamante Juan M, Rivarola Héctor W, Fernández Alicia R, Enders Julio E, Fretes Ricardo, Palma José A, Paglini-Oliva Patricia A
Cátedra de Física Biomédica, Facultad de Ciencias Médicas, Universidad Nacional de Córdoba, Santa Rosa 1085, Argentina.
Int J Parasitol. 2002 Jun 15;32(7):889-96. doi: 10.1016/s0020-7519(02)00023-1.
In two murine models we studied Trypanosoma cruzi reinfection in the acute and chronic phase of experimental Chagas' disease in order to elucidate the relevance of reinfections in determining the variability of cardiac symptoms and the irreversible cardiac damage. They were followed for 120 and 600 days post infection (p.i.) for the acute and chronic model, respectively. Reinfected mice reached higher parasitaemia levels than infected mice. The survival was 33 and 21% in the chronic phase for mice reinfected in the acute phase and 13% for mice reinfected in the chronic stage at the end of the experiments. Sixty-six percent of the infected group presented electrocardiographic abnormalities (heart frequency, prolonged PQ segment or QRS complex) in the chronic stage whereas 100% of the reinfected animals exhibited electric cardiac dysfunction since 90 and 390 days p.i. for the acute and chronic reinfected model, respectively (P<0.01). Heart histopathological studies showed fibrosis and necrosis areas and mononuclear infiltrates supporting the view that parasite persistence is a major factor in continuing the tissue inflammation. This work shows that T. cruzi reinfections could be related to the variability and severity of the clinical course of Chagas' disease and that parasite persistence is involved in exacerbation of the disease.
在两个小鼠模型中,我们研究了克氏锥虫在实验性恰加斯病急性期和慢性期的再感染情况,以阐明再感染在确定心脏症状变异性和不可逆心脏损伤方面的相关性。对于急性和慢性模型,分别在感染后120天和600天对小鼠进行跟踪观察。再感染小鼠的寄生虫血症水平高于初次感染小鼠。在实验结束时,急性期再感染的小鼠在慢性期的存活率为33%,慢性期再感染的小鼠存活率为21%,而慢性期再感染的小鼠存活率为13%。66%的初次感染组小鼠在慢性期出现心电图异常(心率、PQ段延长或QRS波群异常),而对于急性和慢性再感染模型,分别在感染后90天和390天起,100%的再感染动物出现心脏功能障碍(P<0.01)。心脏组织病理学研究显示有纤维化和坏死区域以及单核细胞浸润,支持了寄生虫持续存在是导致组织炎症持续的主要因素这一观点。这项研究表明,克氏锥虫再感染可能与恰加斯病临床病程的变异性和严重程度有关,且寄生虫持续存在参与了疾病的加重过程。