A Multi-Epitope Vaccine Designed Against Blood-Stage of Malaria: An Immunoinformatic And Structural Approach
Abstract Malaria is a complex disease caused by genus Plasmodiumis parasites and is the leading cause of morbidity and mortality worldwide. The most severe form of malaria disease is caused by Plasmodium falciparum. A combination of different approaches is needed to control malaria, and on the other hand, resistance to first-line drugs and insecticides makes the need for an effective vaccine more mandatory than ever. Erythrocyte parasites have the most clinical symptoms, so designing the potential vaccine for this stage of infection could be very helpful. In this research, we used various bioinformatics tools to design an effective antibody-inducing multi-epitope vaccine against the blood-stage of malaria infection. For this purpose, we selected the malaria PfGARP protein as the target here. The predicted B and HTL epitopes and flagellin molecule (as an adjuvant) were connected with suitable linkers and the final construct vaccine was designed. The various properties of this construct, including physicochemical properties, 3D structures, molecular docking, molecular simulations, and in silico cloning were then carried out. Based on preliminary findings, our designed fusion construct could be proposed as a novel potential vaccine candidate against Malaria. However, in vitro and in vivo studies are essential for further validation.