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Nifurtimox response of Trypanosoma cruzi isolates from an outbreak of Chagas disease in Caracas, Venezuela

机译:委内瑞拉的Chagas疾病爆发的触发瘤Cruzi的Nifurtimox响应

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Background & objectives: In Venezuela, Chagas disease (ChD) is considered a serious health problem, with about 6 million people at risk; and acute outbreaks due to oral transmission of Chagas Disease (OChD) are becoming increasingly important. In 2007 there was a major outbreak of OChD and although patients from this episode were treated with nifurtimox (Lampit (R)-Bayer), about 70% therapeutic failure was registered. These results led us to examine whether parasite's drug susceptibility was related to this therapeutic failure. Methods: The Trypanosoma cruzi parasites were isolated by haemoculture of the peripheral blood drawn from the pre- and post-nifurtimox treated patients infected in the 2007 OChD outbreak at Caracas, Venezuela. The in vitro assays for drug testing were performed by the MTT methodology followed by calculation of inhibitory concentration-50 (IC50) values. Results: Parasite isolates obtained from the infected patients prior and after nifurtimox treatment when subjected to variable concentrations of the drug showed great heterogeneity in susceptibility with IC50 values ranging from 4.07 +/- 1.82 to 94.92 +/- 7.24 mu M. Interpretation & conclusion: The high heterogeneity in nifurtimox IC50 values in the isolates and clones from the OChD patients, suggests that the therapeutic failure to nifurtimox could be due in part to a phenotypic variability that existed in the wild parasite population at the original source of contamination. Though, further pharmacological studies are needed to confirm the existence of natural nifurtimox resistance in the parasite.
机译:背景与目的:在委内瑞拉,查加斯病(ChD)被认为是一个严重的健康问题,约有600万人处于危险之中;由于恰加斯病(OChD)的口服传播而导致的急性暴发正变得越来越重要。2007年发生了一次重大的OChD暴发,尽管这一事件的患者接受了硝呋替莫(Lampit(R)-拜耳)治疗,但约70%的治疗失败。这些结果促使我们研究寄生虫的药物敏感性是否与治疗失败有关。方法:通过对2007年委内瑞拉加拉加斯OChD暴发期间感染的硝呋替莫治疗前后患者的外周血进行血液培养,分离克鲁兹锥虫寄生虫。采用MTT法进行体外药物试验,然后计算抑制浓度-50(IC50)值。结果:在接受不同浓度的药物治疗之前和之后,从感染患者获得的寄生虫分离物在易感性上表现出很大的异质性,IC50值在4.07+/-1.82到94.92+/-7.24μM之间。解释与结论:来自OChD患者的分离物和克隆物中的nifurtimox IC50值具有高度异质性,表明硝呋替莫治疗失败的部分原因可能是原始污染源野生寄生虫种群中存在的表型变异。不过,还需要进一步的药理学研究来证实疟原虫对硝基苯莫司的天然耐药性。

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