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suck abstract from ncbi


10.1016/j.compbiomed.2021.104420

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suck abstract from ncbi


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pmid33930764      Comput+Biol+Med 2021 ; 133 (ä): 104420
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  • Immunogenomics guided design of immunomodulatory multi-epitope subunit vaccine against the SARS-CoV-2 new variants, and its validation through in silico cloning and immune simulation #MMPMID33930764
  • Khan A; Khan S; Saleem S; Nizam-Uddin N; Mohammad A; Khan T; Ahmad S; Arshad M; Ali SS; Suleman M; Wei DQ
  • Comput Biol Med 2021[Jun]; 133 (ä): 104420 PMID33930764show ga
  • Reports of the novel and more contagious strains of SARS-CoV-2 originating in different countries have further aggravated the pandemic situation. The recent substitutions in spike protein may be critical for the virus to evade the host's immune system and therapeutics that have already been developed. Thus, this study has employed an immunoinformatics pipeline to target the spike protein of this novel strain to construct an immunogenic epitope (CTL, HTL, and B cell) vaccine against the new variant. Our investigation revealed that 12 different epitopes imparted a critical role in immune response induction. This was validated by an exploration of physiochemical properties and experimental feasibility. In silico and host immune simulation confirmed the expression and induction of both primary and secondary immune factors such as IL, cytokines, and antibodies. The current study warrants further lab experiments to demonstrate its efficacy and safety.
  • |*COVID-19[MESH]
  • |*Viral Vaccines[MESH]
  • |Cloning, Molecular[MESH]
  • |Computer Simulation[MESH]
  • |Epitopes, B-Lymphocyte[MESH]
  • |Epitopes, T-Lymphocyte[MESH]
  • |Humans[MESH]
  • |Immunity[MESH]
  • |Molecular Docking Simulation[MESH]
  • |SARS-CoV-2[MESH]
  • |Spike Glycoprotein, Coronavirus/genetics[MESH]


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