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An evaluation of Chloroquine as a broad-acting antiviral against Hand, Foot and Mouth Disease

机译:氯喹的评价作为抗手动,脚和口腔疾病的广泛抗效抗病毒

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Abstract A common childhood affliction of viral origin in young children and immunocompromised adults, the Hand, Foot and Mouth Disease (HFMD) has become a significant public health concern in the Asia-Pacific Region. Characterized by the appearance of vesiculopapular rashes on the hands, feet and mouth, the disease is generally mild and self-limiting. In a minority of cases, patients can develop neurological complications that could result in permanent morbidity or even fatality. In the absence of a specific antiviral for treatment, medical care is limited to supportive and symptomatic relief, presenting a need for more research into an effective antiviral to be used in the management of the disease. In this study, we evaluated the efficacy of chloroquine, a FDA-approved lysosomotropic agent, against several serotypes of HFMD-associated enteroviruses, including EV-A71, in reducing infectious virus production. We have also evaluated chloroquine in a murine model of EV-A71 infection to ascertain its antiviral efficacy in vivo . The results suggest that chloroquine could be a broad-acting antiviral effective against HFMD-associated enteroviruses. Highlights ? Treatment of RD cells with chloroquine before and after virus inoculation inhibits EV71 replication. ? Chloroquine inhibits viral protein translation and infectious progeny production. ? Chloroquine improves the survival of EV71 infected neonatal mice, reduces symptom severity and pathology. ? Treatment of RD cells before and after virus inoculation inhibits replication of multiple serotypes of enteroviruses.
机译:阐述了幼儿病毒起源的常见童年痛苦,手中的患者,脚和口病(HFMD)已成为亚太地区的重大公共卫生问题。特征在于手,脚和嘴巴上的脉冲压疹的外观,疾病一般是轻度和自限制。在少数病例中,患者可以发育神经系统并发症,这可能导致永久性发病率甚至死亡。在没有特定的治疗抗病毒的情况下,医疗保健仅限于支持性和症状的浮雕,提出了需要更多的研究在疾病管理中使用的有效抗病毒。在这项研究中,我们评估了氯喹,FDA批准的溶酶体溶液的疗效,抵抗包括EV-A71在内的HFMD相关肠病病毒的几种血清型,减少传染病病毒生产。我们还在EV-A71感染的小鼠模型中评估了氯喹,以确定其体内抗病毒疗效。结果表明,氯喹可以是针对HFMD相关的肠病病毒的广泛抗病毒性。强调 ?病毒接种前后用氯喹处理RD细胞抑制EV71复制。还氯喹抑制病毒蛋白翻译和传染性后代生产。还氯喹改善了EV71感染的新生小鼠的存活率,降低了症状严重程度和病理学。还病毒接种前后处理RD细胞抑制肠病病毒多种血清型的复制。

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