Evidence map›Paper›PMID 42666984›Full record

ArticleBioImpacts : BI2026

Designing a multi-epitope vaccine against dengue virus-2 using

Marzieh Shokoohi, Ara Manteghi Tafreshi, Milad Mokarami, Saeedeh Akhavan, Reza Mohammadhassan

Abstract read
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Article in BioImpacts : BI, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Marzieh ShokoohiDepartment of Life Sciences Engineering, Faculty of New Sciences & Technologies, University of Tehran, Tehran, Iran.ORCID https://orcid.org/0009-0000-0601-3791
Ara Manteghi TafreshiAmino Techno Gene Private Virtual Lab, Tehran, Iran.
Milad MokaramiStudent Research Committee, Faculty of Medicine, North Khorasan University of Medical Sciences, Bojnurd, Iran.ORCID https://orcid.org/0009-0005-4652-5886
Saeedeh AkhavanDepartment of Biology, School of Basic Sciences, Science and Research Branch, Islamic Azad University (IAU), Tehran, Iran.ORCID https://orcid.org/0000-0003-4402-9983
Reza MohammadhassanAmino Techno Gene Private Virtual Lab, Tehran, Iran.ORCID https://orcid.org/0000-0002-0509-4187

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Dengue virus (DENV), transmitted by Aedes mosquitoes, remains a serious global health threat with an increasing incidence, largely due to its complex epidemiology and the impact of climate change. DENV belongs to the Methods: First, the genome of DENV-2 was analyzed and vaccine candidate proteins were identified by examining properties such as immunogenicity, toxicity, and allergenicity. The secondary and tertiary structures of the vaccine were predicted and validated, and the vaccine interaction with MHC receptors was analyzed through docking. The stability and flexibility of the vaccine were also evaluated by molecular dynamics simulation. Finally, the vaccine gene sequence was optimized for expression in Results: In this study, four proteins were selected from the initial 10 proteins after eliminating those that were allergens, toxins, or had homology to human or mouse proteins. Finally, protein 3 was identified as the source antigen for epitope prediction and vaccine construction. This highly immunogenic, non-toxic, and non-allergenic protein, located in the cytoplasm, was used to design a multi-epitope vaccine that includes selected epitopes, an IL-12 adjuvant, and a His tag. The designed vaccine consisted of 380 amino acids, exhibited a suitable stability index, and possessed a valid three-dimensional structure, with 95.4% of the amino acids located in the preferred region of the Ramachandran map. Docking and dynamic simulations demonstrated a stable interaction between the vaccine and MHC-I and MHC-II receptors. Also, the vaccine gene sequence was cloned into the pBI121 vector for optimal expression in Conclusion: This study demonstrates the potential of computational approaches for developing targeted vaccines against dengue fever. Additionally, molecular farming offers a promising, safe, and cost-effective method for large-scale production of vaccines. Future research should focus on preclinical and clinical trials to validate the safety and efficacy of the vaccine.

Indexed as

Dengue feverDengue virus 2Molecular farmingMulti-epitope vaccineVaccine development

Identifiers

PMID42666984
PMCPMC13523977

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.