首页> 外文期刊>Journal of immunology research. >A Multiagent Alphavirus DNA Vaccine Delivered by Intramuscular Electroporation Elicits Robust and Durable Virus-Specific Immune Responses in Mice and Rabbits and Completely Protects Mice against Lethal Venezuelan, Western, and Eastern Equine Encephalitis Virus Aerosol Challenges
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A Multiagent Alphavirus DNA Vaccine Delivered by Intramuscular Electroporation Elicits Robust and Durable Virus-Specific Immune Responses in Mice and Rabbits and Completely Protects Mice against Lethal Venezuelan, Western, and Eastern Equine Encephalitis Virus Aerosol Challenges

机译:通过肌内电穿孔提供的多元素alphavirus DNA疫苗,在小鼠和兔子中引发鲁棒和耐用的病毒特异性免疫应答,并完全保护小鼠免受致死乙烯基,西部和东部大当量的患者气溶胶挑战

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摘要

There remains a need for vaccines that can safely and effectively protect against the biological threat agents Venezuelan (VEEV), western (WEEV), and eastern (EEEV) equine encephalitis virus. Previously, we demonstrated that a VEEV DNA vaccine that was optimized for increased antigen expression and delivered by intramuscular (IM) electroporation (EP) elicited robust and durable virus-specific antibody responses in multiple animal species and provided complete protection against VEEV aerosol challenge in mice and nonhuman primates. Here, we performed a comparative evaluation of the immunogenicity and protective efficacy of individual optimized VEEV, WEEV, and EEEV DNA vaccines with that of a 1  1  1 mixture of these vaccines, which we have termed the 3-EEV DNA vaccine, when delivered by IM EP. The individual DNA vaccines and the 3-EEV DNA vaccine elicited robust and durable virus-specific antibody responses in mice and rabbits and completely protected mice from homologous VEEV, WEEV, and EEEV aerosol challenges. Taken together, the results from these studies demonstrate that the individual VEEV, WEEV, and EEEV DNA vaccines and the 3-EEV DNA vaccine delivered by IM EP provide an effective means of eliciting protection against lethal encephalitic alphavirus infections in a murine model and represent viable next-generation vaccine candidates that warrant further development.
机译:仍然需要安全有效地防止生物威胁委内瑞拉(VEEV),西方(WEEV)和东部(EEEV)大肢体脑炎病毒的疫苗。以前,我们证明了针对抗原表达的抗原表达和通过肌内(IM)电穿孔(EP)递送的VEEV DNA疫苗引发了多种动物物种中的鲁棒和耐用的病毒特异性抗体反应,并提供了针对小鼠veev气溶胶挑战的完全保护和非人的灵长类动物。在这里,我们对这些疫苗的111个混合物的单个优化的VEEV,WEEV和EEEV DNA疫苗进行了对比较评估,这些疫苗的111个混合物中,我们称为3-EEV DNA疫苗我是ep。各个DNA疫苗和3-EEV DNA疫苗引发了小鼠和兔的鲁棒和耐用的病毒特异性抗体反应,并从同源VEEV,VEEV和EEEV气溶胶挑战中完全保护小鼠。这些研究的结果表明,IM EP所提供的个体VEEV,WEEV和EEEV DNA疫苗和3-EEV DNA疫苗提供了对鼠模型中致死脑脑梗塞感染的有效手段,并代表可行下一代疫苗候选人提供进一步发展。

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