C-ImmSim was used to simulate the V2’s immunological response.

C-ImmSim was used to simulate the V2’s immunological response.

<p>The development of B-cell populations (A, B), TH-cell populations (C, D), and TC-cell populations (E, F) after three consecutive injections.</p>

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Bibliographic Details
Main Author: Rehana Parvin (841451) (author)
Other Authors: Md. Habib Ullah Masum (13527469) (author), Homaira Pervin Heema (20714921) (author), Aklima Akter (5130614) (author), Mohammad Alamgir Hossain (20714924) (author), A. M. A. M. Zonaed Siddiki (8996447) (author)
Published: 2025
Subjects:
Microbiology
Biotechnology
Immunology
Cancer
Infectious Diseases
Biological Sciences not elsewhere classified
virtual physiological system
significant binding affinity
several computational platforms
gbsa analyses confirmed
following codon optimization
employed computational approaches
28a (+) plasmid
average gc content
designed vaccine candidate
potent ag5 antigen
natural killer cell
div >< p
based vaccine using
based vaccine
grand average
ag5 protein
vaccine ’
tertiary structure
successfully expressed
structurally stable
structural stability
silico </
severe implications
potent epitopes
increased ifn
immune responses
highly soluble
future preclinical
findings highlight
echinococcus </
e </
docked complexes
coli </
cell derived
cai value
animal health
also found
433 ).
34 %)
2 levels
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Description
Summary:<p>The development of B-cell populations (A, B), TH-cell populations (C, D), and TC-cell populations (E, F) after three consecutive injections.</p>

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