Hassan Dariushnejad - Department of Medical Biotechnology, Faculty of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran
Vajihe Ghorbanzadeh - Razi Herbal Medicines Research Center, Lorestan University of Medical Sciences, Khorramabad, Iran
Soheila Akbari - Department of Obstetrics and Gynecology, Lorestan University of Medical Sciences, Khorramabad, Iran
Pejman Hashemzadeh - Department of Medical Biotechnology, Faculty of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran

Background and Aim: SARS-CoV-۲ is the causative agent of Coronavirus ۲۰۱۹ or COVID-۱۹ in the world. Novel coronavirus disease is a respiratory disease. To date, there have been challenges in the treatment for COVID-۱۹ and emerged new variants like UK B۱.۱.۷. Accordingly, an effective prevention regime is needed for this infection, which covers most variants. The purpose of this research was to predict the conserved epitopes of Spike and Nucleocapsid proteins from SARS-CoV-۲ for the design of a novel coronavirus ۲۰۱۹ multi-epitope vaccine using in silico tools. Materials and Methods: Computational analysis and immunoinformatics approaches include identification of potential conserve epitopes and selection of epitopes based on allergenicity, toxicity, antigenicity, and molecular docking were used for epitope prediction and screening. In the next step, selected segments of the epitopes were attached by the suitable linkers. Finally, Maltese-bound protein (MBP) as an adjuvant was added to the novel vaccine structure. The secondary and third structures of the designed multi-epitope vaccine were predicted via immunoinformatics algorithms. Predicted structure refined and validated for attaining best stability. In the end, immunoinformatics evaluation, molecular docking, and molecular dynamics were performed to confirm vaccine efficiency. Codon optimization and in silico cloning were done to ensure the expression yield of the novel multi-epitope vaccine in the target host. Results:  This study showed that our data support the suggestion that the designed vaccine could induce immune responses against SARS-CoV-۲ variants. Conclusion:  The structure designed had acceptable quality with software reviews. Further in vitro and in vivo experiments are needed to confirm the safety and immunogenicity of the candidate vaccine.

B۱.۱.۷ variant, COVID-۱۹, Immunoinformatics, SARS-CoV-۲, Vaccine, ایمونو انفورماتیک, کووید-۱۹, واکسن, SARS-CoV-۲, واریانت B۱.۱.۷