a Virology Division, United States Army Medical Research Institute of Infectious diseases (USAMRIID) , Fort Detrick , MD , USA.
b Pathology Division, United States Army Medical Research Institute of Infectious diseases (USAMRIID) , Fort Detrick , MD , USA.
Hum Vaccin Immunother. 2017 Dec 2;13(12):2902-2911. doi: 10.1080/21645515.2017.1356500. Epub 2017 Oct 18.
Lassa virus (LASV) is an ambisense RNA virus in the Arenaviridae family and is the etiological agent of Lassa fever, a severe hemorrhagic disease endemic to West and Central Africa. There are no US Food and Drug Administration (FDA)-licensed vaccines available to prevent Lassa fever. in our previous studies, we developed a gene-optimized DNA vaccine that encodes the glycoprotein precursor gene of LASV (Josiah strain) and demonstrated that 3 vaccinations accompanied by dermal electroporation protected guinea pigs from LASV-associated illness and death. Here, we describe an initial efficacy experiment in cynomolgus macaque nonhuman primates (NHPs) in which we followed an identical 3-dose vaccine schedule that was successful in guinea pigs, and a follow-on experiment in which we used an accelerated vaccination strategy consisting of 2 administrations, spaced 4 weeks apart. In both studies, all of the LASV DNA-vaccinated NHPs survived challenge and none of them had measureable, sustained viremia or displayed weight loss or other disease signs post-exposure. Three of 10 mock-vaccinates survived exposure to LASV, but all of them became acutely ill post-exposure and remained chronically ill to the study end point (45 d post-exposure). Two of the 3 survivors experienced sensorineural hearing loss (described elsewhere). These results clearly demonstrate that the LASV DNA vaccine combined with dermal electroporation is a highly effective candidate for eventual use in humans.
拉萨病毒(LASV)是一种负义 RNA 病毒,属于 Arenaviridae 科,是拉沙热的病原体,拉沙热是一种严重的出血性疾病,流行于西非和中非。目前尚无美国食品和药物管理局(FDA)批准的疫苗可预防拉沙热。在我们之前的研究中,我们开发了一种基因优化的 DNA 疫苗,该疫苗编码 LASV 的糖蛋白前体基因(Josiah 株),并证明 3 次疫苗接种伴随皮内电穿孔可保护豚鼠免受 LASV 相关疾病和死亡的侵害。在这里,我们描述了在食蟹猴非人灵长类动物(NHP)中的首次疗效实验,我们遵循了与豚鼠相同的 3 剂疫苗接种方案,该方案在豚鼠中取得了成功,随后进行了一项后续实验,我们使用了 2 次间隔 4 周的加速疫苗接种策略。在这两项研究中,所有接受 LASV DNA 疫苗接种的 NHP 在接受挑战后均存活下来,并且没有可测量的持续病毒血症,也没有出现体重减轻或其他疾病迹象。在 LASV 暴露后,10 名模拟接种疫苗的动物中有 3 只存活,但所有动物在暴露后均出现急性疾病,并持续到研究终点(暴露后 45 天)。3 名幸存者中的 2 人经历了感觉神经性听力损失(在其他地方描述)。这些结果清楚地表明,LASV DNA 疫苗与皮内电穿孔相结合是一种非常有效的候选疫苗,最终可用于人类。