Multi-pathogen based chimeric vaccine to fight against COVID-19 and concomitant coinfections
Original Research Paper
Molecular Docking Simulation
COVID-19 Vaccines
SARS-CoV-2
Coinfection
Vaccines, Subunit
Humans
COVID-19
Epitopes, T-Lymphocyte
Epitopes, B-Lymphocyte
Computational Biology
Viral Vaccines
3. Good health
DOI:
10.1007/s10529-023-03380-0
Publication Date:
2023-05-06T09:02:17Z
AUTHORS (6)
ABSTRACT
COVID-19 has proved to be a fatal disease of the year 2020, due to which thousands of people globally have lost their lives, and still, the infection cases are at a high rate. Experimental studies suggested that SARS-CoV-2 interacts with various microorganisms, and this coinfection is accountable for the augmentation of infection severity.In this study, we have designed a multi-pathogen vaccine by involving the immunogenic proteins from S. pneumonia, H. influenza, and M. tuberculosis, as they are dominantly associated with SARS-CoV-2. A total of 8 antigenic protein sequences were selected to predict B-cell, HTL, and CTL epitopes restricted to the most prevalent HLA alleles. The selected epitopes were antigenic, non-allergenic, and non-toxic and were linked with adjuvant and linkers to make the vaccine protein more immunogenic, stable, and flexible. The tertiary structure, Ramachandran plot, and discontinuous B-cell epitopes were predicted. Docking and MD simulation study has shown efficient binding of the chimeric vaccine with the TLR4 receptor.The in silico immune simulation analysis has shown a high level of cytokines and IgG after a three-dose injection. Hence, this strategy could be a better way to decrease the disease's severity and could be used as a weapon to prevent this pandemic.
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