Abdi Sayed Aliul Hasan, Ali Amena, Sayed Shabihul Fatma, Ali Abuzer, Alam Prawez
Department of Pharmacy, Al Baha University, Al Baha 1988, Saudi Arabia.
Department of Pharmaceutical Chemistry, College of Pharmacy, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.
Vaccines (Basel). 2022 Sep 19;10(9):1564. doi: 10.3390/vaccines10091564.
Currently, there are limited treatment options available for the monkeypox disease. We used a computational strategy to design a specific antigenic vaccine against pathogens. After using various immunoinformatic tools and filters, cytotoxic T-cell lymphocyte (CTL)-, helper T-cell lymphocyte (HTL)-, and interferon gamma (IFN-γ)-inducing epitopes, which comprised the vaccine, in addition to other parameters, such as antigenic and allergic profiles, were assessed to confirm the safety of the vaccine. However, vaccine interaction and stability with Toll-like receptors (TLRs) were assessed by dynamic simulation methods, and it was found that the constructed vaccine was stable. In addition, C-IMMSIM tools were used to determine the immune-response-triggering capabilities of the vaccine. These immunoinformatic findings reveal that constructed vaccine candidates may be capable of triggering an efficient immune response for monkeypox viral infections. However, experimental evaluation is required to verify the safety and immunogenic profile of constructed vaccines.
目前,猴痘疾病的治疗选择有限。我们采用了一种计算策略来设计针对病原体的特异性抗原疫苗。在使用各种免疫信息学工具和筛选方法后,除了抗原性和过敏特征等其他参数外,还对构成疫苗的细胞毒性T淋巴细胞(CTL)、辅助性T淋巴细胞(HTL)和干扰素γ(IFN-γ)诱导表位进行了评估,以确认疫苗的安全性。然而,通过动态模拟方法评估了疫苗与Toll样受体(TLR)的相互作用和稳定性,发现构建的疫苗是稳定的。此外,使用C-IMMSIM工具来确定疫苗引发免疫反应的能力。这些免疫信息学研究结果表明,构建的候选疫苗可能能够引发针对猴痘病毒感染的有效免疫反应。然而,需要进行实验评估来验证构建疫苗的安全性和免疫原性特征。