Department of Pediatrics, Teikyo University School of Medicine, 2-11-1 Kaga, Itabashi-ku, Tokyo, 173-8605, Japan.
School of Tropical Medicine and Global Health, Nagasaki University, 1-12-4 Sakamoto, Nagasaki, 852-8523, Japan.
Eur J Clin Microbiol Infect Dis. 2021 Sep;40(9):1815-1820. doi: 10.1007/s10096-021-04230-5. Epub 2021 Mar 26.
Alveolar echinococcosis (AE) is caused by the larval stage of Echinococcus multilocularis. Chemotherapy for AE involves albendazole (ABZ), which has shown insufficient efficacy. More effective chemotherapy for AE is needed. Previously, we have demonstrated that atovaquone (ATV), an antimalarial, inhibits mitochondrial complex III of E. multilocularis and restricts the development of larval cysts in in vivo experiments. Therefore, in this study, we evaluated the efficacy of ABZ and ATV combination therapy on E. multilocularis in culture and in vivo experiments. Protoscoleces were treated with 50 μM ABZ and/or ATV in the medium; the duration of parasite elimination was determined under aerobic and anaerobic culture. In the in vivo experiment, the effects of ABZ and ATV combination treatment in BALB/c mice infected orally with eggs from the feces of an adult-stage E. multilocularis-infected dog were compared with those of standard oral ABZ therapy. In the culture assay, the duration of elimination associated with ABZ and ATV combination treatment was shorter than that associated with ATV alone under aerobic conditions. Protoscolex viability progressively reduced owing to the combination treatment under anaerobic conditions; however, either drug used singly did not exhibit antiparasitic effects under hypoxia. Furthermore, compared with ABZ alone, the combination treatment significantly reduced the growth of the primary cyst in the liver of mice infected orally with parasite eggs (P = .011). ATV enhances the effect of ABZ in the treatment of AE in mice.
泡型包虫病(AE)是由细粒棘球绦虫的幼虫阶段引起的。AE 的化学疗法涉及阿苯达唑(ABZ),但其疗效不足。需要更有效的 AE 化学疗法。此前,我们已经证明抗疟药阿托伐醌(ATV)抑制细粒棘球绦虫的线粒体复合物 III,并限制幼虫囊肿在体内实验中的发展。因此,在这项研究中,我们评估了 ABZ 和 ATV 联合治疗对培养物和体内实验中细粒棘球蚴的疗效。用 50μM ABZ 和/或 ATV 处理原头节;在有氧和无氧培养下确定寄生虫消除的持续时间。在体内实验中,比较了 ABZ 和 ATV 联合治疗感染成年期感染犬粪便卵的 BALB/c 小鼠与标准口服 ABZ 治疗的效果。在培养测定中,ABZ 和 ATV 联合治疗的消除时间短于有氧条件下单独使用 ATV 的消除时间。由于联合治疗,原头节活力在缺氧条件下逐渐降低;然而,单独使用任何一种药物在缺氧条件下均无抗寄生虫作用。此外,与单独使用 ABZ 相比,联合治疗显著降低了经口感染寄生虫卵的小鼠肝脏中原发性囊肿的生长(P=0.011)。ATV 增强了 ABZ 在治疗 AE 中的作用。