Lab. de Fisiología de Parásitos, Centro de Biofísica y Bioquímica, IVIC, Caracas 1020A, Venezuela.
Exp Parasitol. 2013 Aug;134(4):422-9. doi: 10.1016/j.exppara.2013.05.006. Epub 2013 May 14.
Chagas disease, caused by the intracellular protozoan Trypanosoma cruzi, is associated with inflammation, discomfort and pain during the acute phase. The influence of TNF-α (tumor necrosis factor) in this disease outcome is controversial. In this way, the aim of this work was to determine the role of the TNF-α blocker etanercept in the pain, discomfort, and survival during the Chagas' acute phase of mice experimentally infected with a wild virulent strain of T. cruzi. The infection with this wild strain was responsible for a severe visceral inflammation and said parasite showed a tropism in peritoneal fluid cells. Etanercept was able to restore spontaneous vertical and horizontal activities during the second week after infection and to abolish mechanical allodynia during the first week after infection. Finally, etanercept delayed the mortality without any effect on the parasitemia rates. This is the first report that correlates sickness behavior and allodynia with TNF-α and suggests that this cytokine may play an important role in the physiopathology of the acute phase.
恰加斯病由细胞内原生动物克氏锥虫引起,与急性阶段的炎症、不适和疼痛有关。TNF-α(肿瘤坏死因子)在这种疾病结果中的影响存在争议。因此,本工作的目的是确定 TNF-α 阻断剂依那西普在实验感染野生毒力株克氏锥虫的小鼠恰加斯病急性期中疼痛、不适和生存中的作用。这种野生株的感染导致严重的内脏炎症,并且寄生虫在腹腔液细胞中表现出亲嗜性。依那西普能够在感染后第二周恢复自发垂直和水平活动,并在感染后第一周消除机械性感觉过敏。最后,依那西普延迟了死亡率,而对寄生虫血症率没有任何影响。这是首次将疾病行为和感觉过敏与 TNF-α 相关联的报告,并表明该细胞因子可能在急性期中的病理生理学中发挥重要作用。