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An inactivated hand-foot-and-mouth disease vaccine using the enterovirus 71 (C4a) strain isolated from a Korean patient induces a strong immunogenic response in mice

机译:使用从一名韩国患者中分离出的肠道病毒71(C4a)株灭活的手足口病疫苗可在小鼠中诱导强烈的免疫原性应答

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摘要

Enterovirus 71 (EV71) is a major causative agent of hand-foot-and-mouth disease (HFMD) frequently occurring in children. HFMD induced by EV71 can cause serious health problems and has been reported worldwide, particularly in the Asia-Pacific region. In this study, we assessed the immunogenicity of a formalin-inactivated HFMD vaccine using an EV71 strain (FI-EV71 C4a) isolated from a Korean patient. The vaccine candidate was evaluated in mice to determine the vaccination doses and vaccine schedules. BALB/c mice were intramuscularly administered 5, 10, or 20 μg FI-EV71 vaccine, followed by a booster 2 weeks later. EV71-specific antibodies and neutralizing antibodies were induced and maintained until the end of the experimental period in all vaccinated groups. To determine the effectiveness of adjuvant for the EV71 vaccine, three adjuvants, i.e., aluminium hydroxide gel, monophosphoryl lipid A, and polyinosinic-polycytidylic acid, were administered separately with the FI-EV71 vaccine to mice via the intramuscular route. Mice administered the FI-EV71 vaccine formulated with all three adjuvants induced a significantly increased antibody response compared with that of the single adjuvant groups. The vaccinated group with triple adjuvants exhibited more rapid induction of EV71-specific and neutralizing antibodies than the other groups. These results suggested that the role of adjuvant in inactivated vaccine was important for eliciting effective immune responses against EV71. In conclusion, our results showed that FI-EV71 was a potential candidate vaccine for prevention of EV71 infection.
机译:肠病毒71(EV71)是儿童经常发生的手足口病(HFMD)的主要病原体。 EV71引起的手足口病可引起严重的健康问题,并且在世界范围内都有报道,特别是在亚太地区。在这项研究中,我们使用从韩国患者身上分离的EV71株(FI-EV71 C4a)评估了福尔马林灭活的HFMD疫苗的免疫原性。在小鼠中评估候选疫苗,以确定疫苗接种剂量和疫苗时间表。向BALB / c小鼠肌肉内注射5、10或20μgFI-EV71疫苗,然后在2周后加强免疫。在所有接种组中,EV71特异性抗体和中和抗体被诱导并维持到实验期结束。为了确定佐剂对EV71疫苗的有效性,将三种佐剂,即氢氧化铝凝胶,单磷酰脂质A和多肌苷-聚胞苷酸与FI-EV71疫苗分别通过肌内途径给予小鼠。与单一佐剂组相比,给予所有三种佐剂配制的FI-EV71疫苗的小鼠诱导了明显增强的抗体应答。接种三重佐剂的组比其他组表现出更快的EV71特异性和中和抗体诱导。这些结果表明佐剂在灭活疫苗中的作用对于引发针对EV71的有效免疫应答非常重要。总之,我们的结果表明,FI-EV71是预防EV71感染的潜在候选疫苗。

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