Alamri Abdulaziz, Almutairi Saeedah, Al Rokayan Salman, Zaky Mohamed Y, Abdel-Maksoud Mostafa A, Fatima Israr
Biochemistry Department, College of Science, King Saud University, Riyadh, Saudi Arabia.
Botany and Microbiology Department, College of Science, King Saud University, Riyadh, Saudi Arabia.
Mol Divers. 2025 Jul 15. doi: 10.1007/s11030-025-11249-9.
The Arenaviridae family of viruses includes the Machupo virus (MACV), which is associated with the potentially fatal Bolivian hemorrhagic fever, a disease with a mortality rate of 15%-30% depending on the speed of diagnosis and the availability of health facilities. To date, there is no licensed vaccine available for MACV, highlighting the need for a preventive measure. In this work, we use immunoinformatics approaches to create a multi-epitope vaccine based on the most dominant MACV proteins. For constructational epitopes, we selected glycoprotein precurssor (GP), nucleoprotein (NP), RNA-dependant RNA polymerase (L), and Zinc-binding RING finger protein (Z) from garner the proteins essential for replicating and invading a host cell. Using in silico prediction methods, a total of thirteen T-cell epitopes (seven MHC class I and six MHC class II binders) and eight B-cell epitopes were identified as having the greatest potential to elicit strong and broad-spectrum immune responses. These selected epitopes were validated in silico to ensure the highest degree of immunogenicity and no allergenic or toxic effects. To increase the potential of the vaccine to elicit an immune response, the 50S ribosomal protein L7/L12 was added as an adjuvant. The analysis of population coverage indicated that the epitopes could provide immunological protection to nearly 98.04% of the world population. The theoretical vaccine design included 3D modeling and simulation of docking to immunoreceptors like Toll-like receptor 4 (TLR4) and MHC molecules, which confirmed their stable and high-affinity binding interactions. The results from in silico simulations of the immune response also showed abundant production of antibodies and strong engagement of various T-cell subsets. In summary, this study proposes a multi-epitope Machupo virus vaccine candidate that can be tested in the lab to evaluate its effectiveness as a preventative measure for Bolivian hemorrhagic fever.
沙粒病毒科病毒包括马丘波病毒(MACV),它与具有潜在致命性的玻利维亚出血热有关,这种疾病的死亡率在15%至30%之间,具体取决于诊断速度和医疗设施的可及性。迄今为止,尚无针对马丘波病毒的许可疫苗,这凸显了采取预防措施的必要性。在这项研究中,我们运用免疫信息学方法,基于马丘波病毒最主要的蛋白质构建一种多表位疫苗。对于构建表位,我们从获取的用于复制和侵入宿主细胞的必需蛋白质中选择了糖蛋白前体(GP)、核蛋白(NP)、RNA依赖性RNA聚合酶(L)和锌结合环指蛋白(Z)。通过计算机预测方法,总共鉴定出13个T细胞表位(7个MHC I类结合表位和6个MHC II类结合表位)以及8个B细胞表位,它们最有可能引发强烈且广谱的免疫反应。这些选定的表位在计算机上进行了验证,以确保具有最高程度的免疫原性,且无过敏或毒性作用。为提高疫苗引发免疫反应的潜力,添加了50S核糖体蛋白L7/L12作为佐剂。群体覆盖率分析表明,这些表位可为全球近98.04%的人口提供免疫保护。理论疫苗设计包括对与Toll样受体4(TLR4)和MHC分子等免疫受体对接的3D建模和模拟,这证实了它们稳定且高亲和力的结合相互作用。免疫反应的计算机模拟结果还显示抗体大量产生以及各种T细胞亚群的强烈参与。总之,本研究提出了一种多表位马丘波病毒疫苗候选物,可在实验室中进行测试,以评估其作为玻利维亚出血热预防措施的有效性。