Laboratório de Doenças Parasitárias, Escola de Medicina & Núcleo de Pesquisas em Ciências Biológicas, Universidade Federal de Ouro Preto, Minas Gerais, Brazil
Laboratório de Parasitologia Básica, Instituto de Ciências Biomédicas, Universidade Federal de Alfenas, Alfenas, Minas Gerais, Brazil.
Antimicrob Agents Chemother. 2018 May 25;62(6). doi: 10.1128/AAC.00401-18. Print 2018 Jun.
Combination therapy has been proposed as an alternative therapeutic approach for the treatment of Chagas disease. In this study, we evaluated the effect of treatment with benznidazole combined with E1224 (ravuconazole prodrug) in an experimental murine model of acute infection. The first set of experiments assessed the range of E1224 doses required to induce parasitological cure using strains with different susceptibilities to benznidazole (Y and Colombian). All E1224 doses were effective in suppressing the parasitemia and preventing death; however, parasitological cure was observed only in mice infected with Y strain. Considering these results, we evaluated the effect of combined treatment against Colombian, a multidrug-resistant strain. After exclusion of antagonistic effects using assays, infected mice were treated with E1224 and benznidazole in monotherapy or in combination at day 4 or 10 postinoculation. All treatments were well tolerated and effective in suppressing parasitemia; however, parasitological and PCR assays indicated no cure among mice treated with monotherapies. Intriguingly, the outcome of combination therapy was dependent on treatment onset. Early treatment using optimal doses of E1224-benznidazole induced a 100% cure rate, but this association could not eliminate a well-established infection. The beneficial effect of combination therapy was evidenced by further reductions of the patent parasitemia period in the group receiving combined therapy compared with monotherapies. Our results demonstrated a positive interaction between E1224 and benznidazole against murine infection using a multidrug-resistant strain and highlighted the importance of a stringent experimental model in the evaluation of new therapies.
联合治疗已被提议作为治疗恰加斯病的一种替代治疗方法。在这项研究中,我们评估了用苯硝唑联合 E1224(雷夫康唑前药)治疗急性感染实验性小鼠模型的效果。第一组实验评估了使用对苯硝唑敏感性不同的(Y 和哥伦比亚)株来诱导寄生虫学治愈所需的 E1224 剂量范围。所有 E1224 剂量均有效抑制寄生虫血症并预防死亡;然而,仅在感染 Y 株的小鼠中观察到寄生虫学治愈。考虑到这些结果,我们评估了联合治疗对抗哥伦比亚(一种多药耐药株)的效果。在用 测定排除拮抗作用后,在感染后第 4 或 10 天用 E1224 和苯硝唑单独或联合治疗感染的小鼠。所有治疗均耐受良好,有效抑制寄生虫血症;然而,寄生虫学和 PCR 检测表明,单独治疗的小鼠未治愈。有趣的是,联合治疗的结果取决于治疗开始时间。早期使用 E1224-苯硝唑的最佳剂量进行联合治疗可诱导 100%的治愈率,但这种关联不能消除已建立的感染。与单独治疗相比,联合治疗组的专利寄生虫血症期进一步缩短,证明了联合治疗的有益效果。我们的结果表明,使用多药耐药株对 E1224 和苯硝唑对小鼠 感染具有积极的相互作用,并强调了在评估新疗法时严格的实验模型的重要性。