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肌肉内电穿孔传递的多价丙型肝炎病毒 DNA 疫苗在小鼠和兔中引发强大且持久的病毒特异性免疫应答,并完全保护小鼠免受致死性委内瑞拉、西部和东部马脑炎病毒气溶胶挑战。

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.

机构信息

United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702-5011, USA.

Ichor Medical Systems, Inc., San Diego, CA 92121-3209, USA.

出版信息

J Immunol Res. 2018 Jun 3;2018:8521060. doi: 10.1155/2018/8521060. eCollection 2018.

Abstract

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.

摘要

仍然需要能够安全、有效地预防委内瑞拉(VEEV)、西部(WEEV)和东部(EEEV)马脑炎病毒的疫苗。此前,我们证明了一种经过优化以增加抗原表达并通过肌肉内(IM)电穿孔(EP)递送的 VEEV DNA 疫苗,在多种动物物种中引发了强大而持久的病毒特异性抗体反应,并为小鼠和非人类灵长类动物提供了针对 VEEV 气溶胶挑战的完全保护。在这里,我们对个体优化的 VEEV、WEEV 和 EEEV DNA 疫苗的免疫原性和保护效力进行了比较评估,这些疫苗通过 IM EP 递送时,与我们称为 3-EEV DNA 疫苗的这些疫苗的 1:1:1 混合物进行了比较。个体 DNA 疫苗和 3-EEV DNA 疫苗在小鼠和兔中引发了强大而持久的病毒特异性抗体反应,并完全保护小鼠免受同源 VEEV、WEEV 和 EEEV 气溶胶挑战。综上所述,这些研究的结果表明,个体 VEEV、WEEV 和 EEEV DNA 疫苗和通过 IM EP 递送的 3-EEV DNA 疫苗为在小鼠模型中引发针对致命脑炎病毒感染的保护提供了有效的手段,并且是有前途的下一代疫苗候选物,值得进一步开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d0/6008678/891f76221e11/JIR2018-8521060.001.jpg

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