Why the study?
A novel approach using consecutive alternating administration of a triple combination of enterovirus replication inhibitors was characterized for treating enterovirus infections.
Does consecutive alternating administration of a triple combination of anti-enteroviral compounds (pleconaril, MDL-860, and oxoglaucine) improve protective effects and prevent drug resistance in mice infected with coxsackievirus B3?
Does consecutive alternating administration of a triple combination of anti-enteroviral compounds (pleconaril, MDL-860, and oxoglaucine) improve protective effects and prevent drug resistance in mice infected with coxsackievirus B3?
Consecutive alternating administration of a triple antiviral combination provides significant protection and prevents drug resistance in a murine model of coxsackievirus B3 infection.
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.
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Stoyanova et al. (2020) studied this question.
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