Evidence map›Paper›PMID 40571886›Full record

ArticleMolecular biotechnology2026

Uncovering the Unique Epitopes: Validation of In-Silico Synthesized Tetravalent Dengue Vaccine (dvac) Through Cloning, Expression, and Immunogenic Analysis.

Sitara Nasar, Saima Iftikhar, Muhammad Shahid Nadeem

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Article in Molecular biotechnology, 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

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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

3 authors.

Sitara NasarSchool of Biological Sciences, University of the Punjab, Lahore, Pakistan.
Saima IftikharSchool of Biological Sciences, University of the Punjab, Lahore, Pakistan. Saima.sbs@pu.edu.pk.ORCID http://orcid.org/0000-0002-0410-6959
Muhammad Shahid NadeemKing Abdulaziz University Jeddah, Jeddah, Saudi Arabia.

Funding

Higher Education Commision, Pakistan NRPU#7136
6 · The paper itself

Abstract

Dengue is an arthropod borne viral illness which infects millions of people each year. Despite the huge global losses, an effective medication is still unavailable against the disease. For vaccine development, reverse vaccinology approach is being tremendously used as it saves time, energy, cost and resources by selecting the potential epitopes for developing an effective vaccine formulation. In our previous study, we have also used reverse vaccinology approach to propose a multi-epitope vaccine formulation (dvac) against dengue, by targeting the conserved epitopes from all of its serotypes. In this study, we have performed population coverage analysis and molecular dynamic simulation studies which predicted that dvac could offer protection to 98.5% of world population against dengue and forms stable interactions with TLR3/TLR4 receptors, respectively. Moreover, we have performed in-lab gene cloning and expression analysis of dvac in Escherichia coli. The purified dvac is subjected to anti-NS1, anti-dNS1 and anti-EDIII antibodies, raised in rabbits, and the ELISA results confirmed the individuality and intactness of the epitopes incorporated in the refolded dvac molecule. The results from this study endorse the use of dvac as a potential dengue vaccine candidate and also support the reverse vaccinology approach for developing novel therapeutic formulations.

Indexed as

DengueDengue VaccinesDengue VirusEpitopesAnimalsAntibodies, ViralCloning, MolecularHumansMolecular Dynamics SimulationRabbitsToll-Like Receptor 3Viral Nonstructural ProteinsAntibodies, ViralDengue VaccinesEpitopesToll-Like Receptor 3Viral Nonstructural ProteinsDenguedvacELISAReverse vaccinology

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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.