Galabov Angel S, Nikolova Ivanka, Vassileva-Pencheva Ralitsa, Stoyanova Adelina
Pril (Makedon Akad Nauk Umet Odd Med Nauki). 2015;36(2):91-9. doi: 10.1515/prilozi-2015-0057.
Human enteroviruses distributed worldwide are causative agents of a broad spectrum of diseases with extremely high morbidity, including a series of severe illnesses of the central nervous system, heart, endocrine pancreas, skeleton muscles, etc., as well as the common cold contributing to the development of chronic respiratory diseases, including the chronic obstructive pulmonary disease. The above mentioned diseases along with the significantly high morbidity and mortality in children, as well as in the high-risk populations (immunodeficiencies, neonates) definitely formulate the chemotherapy as the main tool for the control of enterovirus infections. At present, clinically effective antivirals for use in the treatment of enteroviral infection do not exist, in spite of the large amount of work carried out in this field. The main reason for this is the development of drug resistance. We studied the process of development of resistance to the strongest inhibitors of enteroviruses, WIN compounds (VP1 protein hydrophobic pocket blockers), especially in the models in vivo, Coxsackievirus B (CV-B) infections in mice. We introduced the tracing of a panel of phenotypic markers (MIC50 value, plaque shape and size, stability at 50℃, pathogenicity in mice) for characterization of the drug-mutants (resistant and dependent) as a very important stage in the study of enterovirus inhibitors. Moreover, as a result of VP1 RNA sequence analysis performed on the model of disoxaril mutants of CVB1, we determined the molecular basis of the drug-resistance. The monotherapy courses were the only approach used till now. For the first time in the research for anti-enterovirus antivirals our team introduced the testing of combination effect of the selective inhibitors of enterovirus replication with different mode of action. This study resulted in the selection of a number of very effective in vitro double combinations with synergistic effect and a broad spectrum of sensitive enteroviruses. The most prospective attainment in our examinations in this field was the development of a novel scheme for the combined application of anti-enteroviral substances in coxsackievirus B1 neuroinfection in newborn mice. It consisted of a consecutive, alternating and non simultaneous administration of the substances in the combination. The triple combination - disoxaril- guanidine. HCl-oxoglaucine (DGO) showed a high effectiveness expressed in the marked reduction of the mortality rate in infected mice as compared both to the placebo group, and to the partner compounds used alone every day, and to the same combination applied simultaneously every day. The studies of the drug sensitivity of viral brain isolates from mice treated with DGO combination showed not only preserved, but even increased sensitivity to the drugs included in the combination. Obviously, the consecutive alternating administration of anti-enteroviral substances hinders the occurrence of drug-resistance in the course of the experimental enteroviral infections in mice.
人类肠道病毒分布于世界各地,是多种发病率极高的疾病的病原体,包括一系列中枢神经系统、心脏、内分泌胰腺、骨骼肌等的严重疾病,以及引发慢性呼吸道疾病(包括慢性阻塞性肺疾病)的普通感冒。上述疾病以及儿童和高危人群(免疫缺陷者、新生儿)中显著较高的发病率和死亡率,无疑使化学疗法成为控制肠道病毒感染的主要手段。尽管在该领域开展了大量工作,但目前尚无临床上有效的用于治疗肠道病毒感染的抗病毒药物。主要原因是耐药性的产生。我们研究了对肠道病毒最强抑制剂WIN化合物(VP1蛋白疏水口袋阻滞剂)产生耐药性的过程,尤其是在体内模型中,即小鼠感染柯萨奇病毒B(CV - B)的过程。我们引入了一组表型标记(MIC50值、噬斑形状和大小、50℃稳定性、对小鼠的致病性)的追踪,以表征药物突变体(耐药和依赖型),这是肠道病毒抑制剂研究中非常重要的一个阶段。此外,通过对CVB1的二氯苯醚菊酯突变体模型进行VP1 RNA序列分析,我们确定了耐药性的分子基础。到目前为止,单一疗法疗程是唯一使用的方法。在抗肠道病毒抗病毒药物的研究中,我们团队首次引入了对具有不同作用方式的肠道病毒复制选择性抑制剂的联合效应测试。这项研究筛选出了一些在体外具有协同效应且对多种敏感肠道病毒有效的双重组合。在该领域我们研究中最有前景的成果是开发了一种在新生小鼠柯萨奇病毒B1神经感染中联合应用抗肠道病毒物质的新方案。它包括连续、交替且不同时给药组合中的物质。三联组合——二氯苯醚菊酯 - 盐酸胍 - 氧化青藤碱(DGO)显示出高效性,与安慰剂组、每天单独使用的对照化合物组以及每天同时使用相同组合的组相比,感染小鼠的死亡率显著降低。对用DGO组合治疗的小鼠的病毒脑分离株进行药物敏感性研究表明,其不仅对组合中的药物保持敏感性,甚至敏感性有所增加。显然,连续交替给药抗肠道病毒物质可防止在小鼠实验性肠道病毒感染过程中出现耐药性。