Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, USA.
Department of Microbiology, Immunology, and Molecular Genetics, College of Medicine, University of Kentucky, Lexington, KY, USA.
Emerg Microbes Infect. 2023 Dec;12(2):2239950. doi: 10.1080/22221751.2023.2239950.
Taï Forest virus (TAFV) is a lesser-known ebolavirus that causes lethal infections in chimpanzees and is responsible for a single human case. Limited research has been done on this human pathogen; however, with the recent emergence of filoviruses in West Africa, further investigation and countermeasure development against this virus is warranted. We developed a vesicular stomatitis virus (VSV)-based vaccine expressing the TAFV glycoprotein as the viral antigen and assessed it for protective efficacy in nonhuman primates (NHPs). Following a single high-dose vaccination, NHPs developed antigen-specific binding and neutralizing antibodies as well as modest T cell responses. Importantly, all vaccinated NHPs were uniformly protected from disease after lethal TAFV challenge while the naïve control group succumbed to the disease. Histopathologic lesions consistent with filovirus disease were present in control NHPs but were not observed in vaccinated NHPs. Transcriptional analysis of whole blood samples obtained after vaccination and challenge was performed to gain insight into molecular underpinnings conferring protection. Differentially expressed genes (DEG) detected 7 days post-vaccination were enriched to processes associated with innate immunity and antiviral responses. Only a small number of DEG was detected in vaccinated NHPs post-challenge while over 1,000 DEG were detected in control NHPs at end-stage disease which mapped to gene ontology terms indicative of defense responses and inflammation. Taken together, this data demonstrates the effective single-dose protection of the VSV-TAFV vaccine, and its potential for use in outbreaks.
太福森林病毒(TAFV)是一种鲜为人知的埃博拉病毒,可导致黑猩猩致命感染,且仅造成过一例人类感染。针对这种人类病原体的研究非常有限;然而,随着最近西非出现丝状病毒,有必要对此病毒进行进一步的调查和对策开发。我们开发了一种基于水疱性口炎病毒(VSV)的疫苗,该疫苗表达 TAFV 糖蛋白作为病毒抗原,并在非人类灵长类动物(NHP)中评估其保护效力。单次高剂量接种疫苗后,NHP 产生了针对抗原的结合抗体和中和抗体以及适度的 T 细胞反应。重要的是,所有接种疫苗的 NHP 在致命 TAFV 挑战后均受到均匀保护而免受疾病侵害,而未接种疫苗的对照组则死于该疾病。在接种疫苗和挑战后获得的全血样本中进行了转录分析,以深入了解赋予保护作用的分子基础。接种疫苗后 7 天检测到的差异表达基因(DEG)富集到与先天免疫和抗病毒反应相关的过程中。接种疫苗的 NHP 仅在挑战后检测到少量 DEG,而对照组的 NHP 在疾病末期检测到超过 1000 个 DEG,这些 DEG 映射到防御反应和炎症的基因本体论术语。总之,这些数据表明 VSV-TAFV 疫苗可有效提供单次剂量保护,并有潜力用于暴发。