Related Experiment Video
Updated: Aug 16, 2025

Rapid, Seamless Generation of Recombinant Poxviruses using Host Range and Visual Selection
Published on: May 24, 2020
Multi-Epitope Vaccine Design against Monkeypox Virus via Reverse Vaccinology Method Exploiting Immunoinformatic and
Kunal Bhattacharya1,2, Israa M Shamkh3,4, Mohammad Shahbaz Khan5
1Pratiksha Institute of Pharmaceutical Sciences, Guwahati 781026, Assam, India.
Researchers developed a potential monkeypox virus vaccine using bioinformatics and immunoinformatics. This novel multi-epitope vaccine shows promise for global protection against monkeypox virus, pending further studies.
Area of Science:
- Virology
- Vaccinology
- Bioinformatics
Background:
- Monkeypox virus is a zoonotic orthopox DNA virus of growing global concern.
- No specific vaccine is currently available, necessitating the development of novel preventative strategies.
- Bioinformatics and immunoinformatics approaches offer powerful tools for rapid vaccine design.
Purpose of the Study:
- To design and computationally evaluate a potential vaccine against the monkeypox virus.
- To utilize B-cell and T-cell epitopes for a multi-epitope vaccine construct.
- To assess the vaccine's efficacy, safety, and population coverage through in silico methods.
Main Methods:
- A multi-epitope vaccine was designed using B-cell and T-cell epitopes from the MPXVgp181 strain.
- Computational tools were employed to predict antigenicity, allergenicity, toxicity, and population coverage.
- In silico immune simulations and expression/cloning studies in *E. coli* were performed.
Main Results:
- The vaccine construct was predicted to be antigenic, non-allergenic, and non-toxic.
- High global population coverage and a satisfactory immune response were computationally predicted.
- Successful in silico expression and cloning indicated suitability for large-scale production.
Conclusions:
- A promising multi-epitope vaccine candidate against monkeypox virus was computationally designed.
- The vaccine's in silico profile suggests potential for broad efficacy and safety.
- Further in vitro and in vivo validation is warranted to advance this vaccine towards clinical application.
More Related Videos
05:15Detection of Neutralization-sensitive Epitopes in Antigens Displayed on Virus-Like Particle VLP-Based Vaccines Using a Capture Assay
Published on: February 10, 2022
10:58Production of E. coli-expressed Self-Assembling Protein Nanoparticles for Vaccines Requiring Trimeric Epitope Presentation
Published on: August 21, 2019