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DNA 疫苗可诱导豚鼠对拉沙病毒和埃博拉病毒的个体或同时感染产生持久的保护性免疫。

DNA vaccines elicit durable protective immunity against individual or simultaneous infections with Lassa and Ebola viruses in guinea pigs.

机构信息

a Virology Division, United States Army Medical Research Institute of Infectious diseases (USAMRIID) , Fort Detrick , MD.

b Pathology Division, United States Army Medical Research Institute of Infectious diseases (USAMRIID) , Fort Detrick , MD.

出版信息

Hum Vaccin Immunother. 2017 Dec 2;13(12):3010-3019. doi: 10.1080/21645515.2017.1382780. Epub 2017 Nov 14.

Abstract

We previously developed optimized DNA vaccines against both Lassa fever and Ebola hemorrhagic fever viruses and demonstrated that they were protective individually in guinea pig and nonhuman primate models. In this study, we vaccinated groups of strain 13 guinea pigs two times, four weeks apart with 50 µg of each DNA vaccine or a mock vaccine at discrete sites by intradermal electroporation. Five weeks following the second vaccinations, guinea pigs were exposed to lethal doses of Lassa virus, Ebola virus, or a combination of both viruses simultaneously. None of the vaccinated guinea pigs, regardless of challenge virus and including the coinfected group, displayed weight loss, fever or other disease signs, and all survived to the study endpoint. All of the mock-vaccinated guinea pigs that were infected with Lassa virus, and all but one of the EBOV-infected mock-vaccinated guinea pigs succumbed. In order to determine if the dual-agent vaccination strategy could protect against both viruses if exposures were temporally separated, we held the surviving vaccinates in BSL-4 for approximately 120 days to perform a cross-challenge experiment in which guinea pigs originally infected with Lassa virus received a lethal dose of Ebola virus and those originally infected with Ebola virus were infected with a lethal dose of Lassa virus. All guinea pigs remained healthy and survived to the study endpoint. This study clearly demonstrates that DNA vaccines against Lassa and Ebola viruses can elicit protective immunity against both individual virus exposures as well as in a mixed-infection environment.

摘要

我们先前开发了针对拉沙热和埃博拉出血热病毒的优化 DNA 疫苗,并证明它们在豚鼠和非人类灵长类动物模型中分别具有保护作用。在这项研究中,我们通过皮内电穿孔在离散部位两次(间隔四周)给 13 株豚鼠接种每组 50µg 的每种 DNA 疫苗或模拟疫苗。第二次接种后五周,豚鼠暴露于拉沙病毒、埃博拉病毒或两者同时的致死剂量下。无论挑战病毒如何,包括同时感染的组,所有接种疫苗的豚鼠均未出现体重减轻、发热或其他疾病迹象,并且均存活至研究终点。所有感染拉沙病毒的模拟疫苗接种豚鼠以及除一只感染 EBOV 的模拟疫苗接种豚鼠外,均死亡。为了确定如果暴露时间间隔,双抗原疫苗接种策略是否可以预防这两种病毒,我们将幸存的疫苗接种者置于 BSL-4 中约 120 天,以进行交叉挑战实验,其中最初感染拉沙病毒的豚鼠接受致死剂量的埃博拉病毒,而最初感染埃博拉病毒的豚鼠则感染致死剂量的拉沙病毒。所有豚鼠均保持健康并存活至研究终点。这项研究清楚地表明,针对拉沙病毒和埃博拉病毒的 DNA 疫苗可以针对单独的病毒暴露以及混合感染环境产生保护性免疫。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af21/5718824/377acfbbdc12/khvi-13-12-1382780-g001.jpg

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