Predicted LBL, CTL, and HTL epitopes from BabA, CagA, and VacA proteins for the development of multi-epitope vaccine.

Predicted LBL, CTL, and HTL epitopes from BabA, CagA, and VacA proteins for the development of multi-epitope vaccine.

<p>Predicted LBL, CTL, and HTL epitopes from BabA, CagA, and VacA proteins for the development of multi-epitope vaccine.</p>

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Bibliographic Details
Main Author: Md. Nahian (20571297) (author)
Other Authors: Md. Rasel Khan (20571300) (author), Fabiha Rahman (20691385) (author), Hossain Mohammed Reza (20691388) (author), Imren Bayil (18887023) (author), Tanjum Ahmed Nodee (20691391) (author), Tabassum Basher (20691394) (author), Mostafizur Rahaman Sany (20691397) (author), Rabeya Najnin Munmun (20691400) (author), S. M. Ariful Habib (20691403) (author), Lincon Mazumder (15455463) (author), Mrityunjoy Acharjee (3761959) (author)
Published: 2025
Subjects:
Microbiology
Biotechnology
Immunology
Cancer
Infectious Diseases
Space Science
Biological Sciences not elsewhere classified
Information Systems not elsewhere classified
secondary mrna structure
optimized restriction sites
current drug treatments
control infections caused
computational approaches offer
epitope subunit vaccine
chosen vaccine constructs
licensed vaccines available
epitope subunit vaccines
proposed vaccine candidates
helicobacter pylori </
molecular docking simulations
vaccine candidates
molecular docking
pylori </
safe vaccines
immune simulations
silico </
h </
− 20
viable strategy
viable alternative
vaca ).
structural flexibility
strongly immunogenic
scale production
potent b
population coverage
persistently infects
performed using
peptic ulcers
negative bacterium
mediated immunity
laboratory validation
increased risk
immunoinformatic strategy
human stomach
gastric cancer
favored regions
extremophilic characteristics
evaluated based
designing antigenic
codon adaptation
bacterium make
analyses suggest
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