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从“一分子、一靶点、一疾病”概念到寻找治疗非脊髓灰质炎肠道病毒(NPEV)感染的多靶点疗法

From the "One-Molecule, One-Target, One-Disease" Concept towards Looking for Multi-Target Therapeutics for Treating Non-Polio Enterovirus (NPEV) Infections.

作者信息

Roux Hugo, Touret Franck, Rathelot Pascal, Vanelle Patrice, Roche Manon

机构信息

Aix-Marseille Université, CNRS, ICR UMR_7273, LPCR, Faculté de Pharmacie, 13005 Marseille, France.

Unité des Virus Émergents (UVE: Aix-Marseille Université, Università di Corsica, IRD 190, Inserm 1207, IRBA), 13005 Marseille, France.

出版信息

Pharmaceuticals (Basel). 2024 Sep 16;17(9):1218. doi: 10.3390/ph17091218.

DOI:10.3390/ph17091218
PMID:39338380
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11434921/
Abstract

Non-polio enteroviruses (NPEVs), namely coxsackieviruses (CV), echoviruses (E), enteroviruses (EV), and rhinoviruses (RV), are responsible for a wide variety of illnesses. Some infections can progress to life-threatening conditions in children or immunocompromised patients. To date, no treatments have been approved. Several molecules have been evaluated through clinical trials without success. To overcome these failures, the multi-target directed ligand (MTDL) strategy could be applied to tackle enterovirus infections. This work analyzes registered clinical trials involving antiviral drugs to highlight the best candidates and develops filters to apply to a selection for MTDL synthesis. We explicitly stated the methods used to answer the question: which solution can fight NPEVs effectively? We note the originality and relevance of this proposal in relation to the state of the art in the enterovirus-inhibitors field. Several combinations are possible to broaden the antiviral spectrum and potency. We discuss data related to the virus and data related to each LEAD compound identified so far. Overall, this study proposes a perspective on different strategies to overcome issues identified in clinical trials and evaluate the "MTDL" potential to improve the efficacy of drugs, broaden the antiviral targets, possibly reduce the adverse effects, drug design costs and limit the selection of drug-resistant virus variants.

摘要

非脊髓灰质炎肠道病毒(NPEVs),即柯萨奇病毒(CV)、埃可病毒(E)、肠道病毒(EV)和鼻病毒(RV),可引发多种疾病。某些感染在儿童或免疫功能低下的患者中可能会发展为危及生命的病症。迄今为止,尚无获批的治疗方法。一些分子已通过临床试验进行评估,但未获成功。为克服这些失败,可应用多靶点导向配体(MTDL)策略来应对肠道病毒感染。这项工作分析了涉及抗病毒药物的注册临床试验,以突出最佳候选药物,并开发筛选方法以应用于MTDL合成的选择。我们明确阐述了用于回答问题的方法:哪种解决方案能有效对抗NPEVs?我们注意到该提议相对于肠道病毒抑制剂领域现有技术水平的新颖性和相关性。有几种组合可能会拓宽抗病毒谱和效力。我们讨论了与病毒相关的数据以及与迄今确定的每种先导化合物相关的数据。总体而言,本研究提出了一种关于不同策略的观点,以克服临床试验中发现的问题,并评估“MTDL”在提高药物疗效、拓宽抗病毒靶点、可能减少不良反应、药物设计成本以及限制耐药病毒变体选择方面的潜力。

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