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强力霉素抑制神经亲和性肠道病毒在体外的增殖。

Doxycycline inhibits neurotropic enterovirus proliferation in vitro.

机构信息

School of Public Health, Shandong First Medical University & Shandong Academy of Medical Sciences, Ji'nan 250117, China; Key Laboratory of Emerging Infectious Diseases in Universities of Shandong, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian 271000, China.

School of Clinical and Basic Medical Sciences, Shandong First Medical University & Shandong Academy of Medical Sciences, Ji'nan 250117, China.

出版信息

Virus Res. 2024 Jul;345:199388. doi: 10.1016/j.virusres.2024.199388. Epub 2024 May 16.

DOI:10.1016/j.virusres.2024.199388
PMID:38714218
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11127601/
Abstract

Human enteroviruses (EVs) represent a global public health concern due to their association with a range of serious pediatric illnesses. Despite the high morbidity and mortality exerted by EVs, no broad-spectrum antivirals are currently available. Herein, we presented evidence that doxycycline can inhibit in vitro replication of various neurotropic EVs, including enterovirus A71 (EV-A71), enterovirus D68 (EV-D68), and coxsackievirus (CV)-A6, in a dose-dependent manner. Further investigations indicated that the drug primarily acted at the post-entry stage of virus infection in vitro, with inhibitory effects reaching up to 89 % for EV-A71 when administered two hours post-infection. These findings provide valuable insights for the development of antiviral drugs against EV infections.

摘要

人类肠道病毒(EVs)因其与一系列严重儿科疾病有关,因此成为全球公共卫生关注的焦点。尽管 EVs 会导致高发病率和死亡率,但目前尚无广谱抗病毒药物。在此,我们提供的证据表明,强力霉素可以以剂量依赖的方式抑制多种神经亲和性 EV 的体外复制,包括肠道病毒 A71(EV-A71)、肠道病毒 D68(EV-D68)和柯萨奇病毒(CV)-A6。进一步的研究表明,该药物主要在病毒感染的进入后阶段发挥作用,在感染后两小时给予强力霉素时,对 EV-A71 的抑制作用高达 89%。这些发现为开发针对 EV 感染的抗病毒药物提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb4c/11127601/881d945faca3/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb4c/11127601/c2b7e2d05760/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb4c/11127601/881d945faca3/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb4c/11127601/c2b7e2d05760/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb4c/11127601/881d945faca3/gr2.jpg

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