The Stephan Angeloff Institute of Microbiology, Bulgarian Academy of Sciences, Sofia, 26, Acad. Georgi Bonchev Street, Bulgaria.
Pathog Dis. 2020 Nov 23;78(9). doi: 10.1093/femspd/ftaa065.
A novel approach for treatment of enterovirus infections was characterized. Application of treatment course of consecutive alternating administration (CAA) of triple combination of enterovirus replication inhibitors in experimental infections (20 MLD50) with coxsackievirus B3 (CVB3) strains in newborn mice is presented. It was established that in infection with cardiotropic Woodruff strain the combination of pleconaril, МDL-860 and oxoglaucine (PMO) subjected to the CAA scheme, a significant protective effect was observed. Monotherapeutic courses as well as simultaneously daily applied PMO were without effect. Analogous data were observed at experimental infection with the neurotriopic Nancy strain of CVB3. Following IC50 values of virus samples taken every day from target organs of infected animals during the whole period of study, a drug-resistance was established in monotherapy with compounds-partners in the PMO combination. At courses by the treatment scheme CAA of PMO development of drug-resistance was not established, but an increased susceptibility to the effect of the inhibitor-components in the combination was proven. Toxicity of PMO applied via the CAA scheme and in the monotherapeutic courses in both healthy and CVB3 infected animals was recorded. All data obtained prove the potential of the CAA treatment scheme for development of effective chemotherapy of enterovirus infections.
提出了一种治疗肠病毒感染的新方法。在新生小鼠的柯萨奇 B3(CVB3)病毒实验感染中(20 MLD50),连续交替给药(CAA)的三种肠病毒复制抑制剂三联体的治疗方案应用情况如下。研究结果表明,在心毒性伍尔夫株感染中,采用 CAA 方案的普乐那利、MDL-860 和蓝蓟定(PMO)三联体具有显著的保护作用。单一治疗疗程以及同时每日应用 PMO 均无效。在实验感染神经毒性 Nancy 株 CVB3 时也观察到了类似的数据。在整个研究期间,每天从感染动物的靶器官中采集病毒样本,以 IC50 值为依据,在 PMO 联合用药的单药治疗中发现了耐药性。在 PMO 的 CAA 治疗方案中,耐药性没有发展,但是证明了联合用药中抑制剂成分的敏感性增加。通过 CAA 方案和在健康及 CVB3 感染动物的单一治疗疗程中应用 PMO 的毒性已被记录。所有获得的数据都证明了 CAA 治疗方案在开发肠病毒感染有效化疗方面的潜力。