首页> 美国卫生研究院文献>The Journal of General Virology >Protection from lethal challenge in a neonatal mouse model by circulating recombinant form coxsackievirus A16 vaccine candidates
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Protection from lethal challenge in a neonatal mouse model by circulating recombinant form coxsackievirus A16 vaccine candidates

机译:通过循环重组形式的柯萨奇病毒A16候选疫苗保护新生小鼠模型免受致死性攻击

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摘要

Circulating coxsackievirus A16 (CA16) is a major cause of hand, foot and mouth disease (HFMD) in South-east Asia. At present, there is no vaccine against CA16. Pathogenic animal models that are sensitive to diverse circulating CA16 viruses would be desirable for vaccine development and evaluation. In this study, we isolated and characterized several circulating CA16 viruses from recent HFMD patients. These CA16 viruses currently circulating in humans were highly pathogenic in a newly developed neonatal mouse model; we also observed and analysed the pathogenesis of representative circulating recombinant form CA16 viruses. An inactivated CA16 vaccine candidate, formulated with alum adjuvant and containing submicrogram quantities of viral proteins, protected neonatal mice born to immunized female mice from lethal-dose challenge with a series of CA16 viruses. Further analysis of humoral immunity showed that antibody elicited from both the immunized dams and their pups could neutralize various lethal viruses by a cytopathic effect in vitro. Moreover, viral titres and loads in the tissues of challenged pups in the vaccine group were far lower than those in the control group, and some were undetectable. This lethal-challenge model using pathogenic CA16 viruses and the vaccine candidates that mediated protection in this model could be useful tools for the future development and evaluation of CA16 vaccines.
机译:循环柯萨奇病毒A16(CA16)是东南亚手足口病(HFMD)的主要原因。当前,没有针对CA16的疫苗。对多种循环CA16病毒敏感的病原性动物模型将是疫苗开发和评估所需要的。在这项研究中,我们从最近的手足口病患者中分离并鉴定了几种正在传播的CA16病毒。目前在人类中传播的这些CA16病毒在新开发的新生小鼠模型中具有高致病性。我们还观察并分析了代表性循环重组形式CA16病毒的发病机理。用明矾佐剂配制并含有亚微克量的病毒蛋白的灭活CA16疫苗候选物,可以保护免疫接种的雌性小鼠所生的新生小鼠免受一系列CA16病毒的致命剂量攻击。体液免疫的进一步分析表明,从免疫的母鼠及其幼仔中获得的抗体可以通过体外的细胞病变作用中和各种致死病毒。此外,疫苗组中被攻击的幼犬的组织中的病毒滴度和载量远低于对照组,并且其中一些是无法检测到的。这种使用致病性CA16病毒的致命攻击模型以及在该模型中介导保护的候选疫苗可能是CA16疫苗未来开发和评估的有用工具。

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